NM_007294.4(BRCA1):c.4185+5A>G AND not provided
- Somatic classification
of clinical impact: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Somatic classification
of oncogenicity: - None
- Review status:
- (0/4) 0 stars out of maximum of 4 starsno assertion criteria provided
- Record status:
- current
- Accession:
- RCV000759532.7
Allele description [Variation Report for NM_007294.4(BRCA1):c.4185+5A>G]
NM_007294.4(BRCA1):c.4185+5A>G
- Gene:
- BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
- Variant type:
- single nucleotide variant
- Cytogenetic location:
- 17q21.31
- Genomic location:
- Preferred name:
- NM_007294.4(BRCA1):c.4185+5A>G
- HGVS:
- NC_000017.11:g.43090939T>C
- NG_005905.2:g.127045A>G
- NM_001407571.1:c.3972+5A>G
- NM_001407581.1:c.4185+5A>G
- NM_001407582.1:c.4185+5A>G
- NM_001407583.1:c.4185+5A>G
- NM_001407585.1:c.4185+5A>G
- NM_001407587.1:c.4182+5A>G
- NM_001407590.1:c.4182+5A>G
- NM_001407591.1:c.4182+5A>G
- NM_001407593.1:c.4185+5A>G
- NM_001407594.1:c.4185+5A>G
- NM_001407596.1:c.4185+5A>G
- NM_001407597.1:c.4185+5A>G
- NM_001407598.1:c.4185+5A>G
- NM_001407602.1:c.4185+5A>G
- NM_001407603.1:c.4185+5A>G
- NM_001407605.1:c.4185+5A>G
- NM_001407610.1:c.4182+5A>G
- NM_001407611.1:c.4182+5A>G
- NM_001407612.1:c.4182+5A>G
- NM_001407613.1:c.4182+5A>G
- NM_001407614.1:c.4182+5A>G
- NM_001407615.1:c.4182+5A>G
- NM_001407616.1:c.4185+5A>G
- NM_001407617.1:c.4185+5A>G
- NM_001407618.1:c.4185+5A>G
- NM_001407619.1:c.4185+5A>G
- NM_001407620.1:c.4185+5A>G
- NM_001407621.1:c.4185+5A>G
- NM_001407622.1:c.4185+5A>G
- NM_001407623.1:c.4185+5A>G
- NM_001407624.1:c.4185+5A>G
- NM_001407625.1:c.4185+5A>G
- NM_001407626.1:c.4185+5A>G
- NM_001407627.1:c.4182+5A>G
- NM_001407628.1:c.4182+5A>G
- NM_001407629.1:c.4182+5A>G
- NM_001407630.1:c.4182+5A>G
- NM_001407631.1:c.4182+5A>G
- NM_001407632.1:c.4182+5A>G
- NM_001407633.1:c.4182+5A>G
- NM_001407634.1:c.4182+5A>G
- NM_001407635.1:c.4182+5A>G
- NM_001407636.1:c.4182+5A>G
- NM_001407637.1:c.4182+5A>G
- NM_001407638.1:c.4182+5A>G
- NM_001407639.1:c.4185+5A>G
- NM_001407640.1:c.4185+5A>G
- NM_001407641.1:c.4185+5A>G
- NM_001407642.1:c.4185+5A>G
- NM_001407644.1:c.4182+5A>G
- NM_001407645.1:c.4182+5A>G
- NM_001407646.1:c.4176+5A>G
- NM_001407647.1:c.4176+5A>G
- NM_001407648.1:c.4062+5A>G
- NM_001407649.1:c.4059+5A>G
- NM_001407652.1:c.4185+5A>G
- NM_001407653.1:c.4107+5A>G
- NM_001407654.1:c.4107+5A>G
- NM_001407655.1:c.4107+5A>G
- NM_001407656.1:c.4107+5A>G
- NM_001407657.1:c.4107+5A>G
- NM_001407658.1:c.4107+5A>G
- NM_001407659.1:c.4104+5A>G
- NM_001407660.1:c.4104+5A>G
- NM_001407661.1:c.4104+5A>G
- NM_001407662.1:c.4104+5A>G
- NM_001407663.1:c.4107+5A>G
- NM_001407664.1:c.4062+5A>G
- NM_001407665.1:c.4062+5A>G
- NM_001407666.1:c.4062+5A>G
- NM_001407667.1:c.4062+5A>G
- NM_001407668.1:c.4062+5A>G
- NM_001407669.1:c.4062+5A>G
- NM_001407670.1:c.4059+5A>G
- NM_001407671.1:c.4059+5A>G
- NM_001407672.1:c.4059+5A>G
- NM_001407673.1:c.4059+5A>G
- NM_001407674.1:c.4062+5A>G
- NM_001407675.1:c.4062+5A>G
- NM_001407676.1:c.4062+5A>G
- NM_001407677.1:c.4062+5A>G
- NM_001407678.1:c.4062+5A>G
- NM_001407679.1:c.4062+5A>G
- NM_001407680.1:c.4062+5A>G
- NM_001407681.1:c.4062+5A>G
- NM_001407682.1:c.4062+5A>G
- NM_001407683.1:c.4062+5A>G
- NM_001407684.1:c.4185+5A>G
- NM_001407685.1:c.4059+5A>G
- NM_001407686.1:c.4059+5A>G
- NM_001407687.1:c.4059+5A>G
- NM_001407688.1:c.4059+5A>G
- NM_001407689.1:c.4059+5A>G
- NM_001407690.1:c.4059+5A>G
- NM_001407691.1:c.4059+5A>G
- NM_001407692.1:c.4044+5A>G
- NM_001407694.1:c.4044+5A>G
- NM_001407695.1:c.4044+5A>G
- NM_001407696.1:c.4044+5A>G
- NM_001407697.1:c.4044+5A>G
- NM_001407698.1:c.4044+5A>G
- NM_001407724.1:c.4044+5A>G
- NM_001407725.1:c.4044+5A>G
- NM_001407726.1:c.4044+5A>G
- NM_001407727.1:c.4044+5A>G
- NM_001407728.1:c.4044+5A>G
- NM_001407729.1:c.4044+5A>G
- NM_001407730.1:c.4044+5A>G
- NM_001407731.1:c.4044+5A>G
- NM_001407732.1:c.4044+5A>G
- NM_001407733.1:c.4044+5A>G
- NM_001407734.1:c.4044+5A>G
- NM_001407735.1:c.4044+5A>G
- NM_001407736.1:c.4044+5A>G
- NM_001407737.1:c.4044+5A>G
- NM_001407738.1:c.4044+5A>G
- NM_001407739.1:c.4044+5A>G
- NM_001407740.1:c.4041+5A>G
- NM_001407741.1:c.4041+5A>G
- NM_001407742.1:c.4041+5A>G
- NM_001407743.1:c.4041+5A>G
- NM_001407744.1:c.4041+5A>G
- NM_001407745.1:c.4041+5A>G
- NM_001407746.1:c.4041+5A>G
- NM_001407747.1:c.4041+5A>G
- NM_001407748.1:c.4041+5A>G
- NM_001407749.1:c.4041+5A>G
- NM_001407750.1:c.4044+5A>G
- NM_001407751.1:c.4044+5A>G
- NM_001407752.1:c.4044+5A>G
- NM_001407838.1:c.4041+5A>G
- NM_001407839.1:c.4041+5A>G
- NM_001407841.1:c.4041+5A>G
- NM_001407842.1:c.4041+5A>G
- NM_001407843.1:c.4041+5A>G
- NM_001407844.1:c.4041+5A>G
- NM_001407845.1:c.4041+5A>G
- NM_001407846.1:c.4041+5A>G
- NM_001407847.1:c.4041+5A>G
- NM_001407848.1:c.4041+5A>G
- NM_001407849.1:c.4041+5A>G
- NM_001407850.1:c.4044+5A>G
- NM_001407851.1:c.4044+5A>G
- NM_001407852.1:c.4044+5A>G
- NM_001407853.1:c.3972+5A>G
- NM_001407854.1:c.4185+5A>G
- NM_001407858.1:c.4185+5A>G
- NM_001407859.1:c.4185+5A>G
- NM_001407860.1:c.4182+5A>G
- NM_001407861.1:c.4182+5A>G
- NM_001407862.1:c.3984+5A>G
- NM_001407863.1:c.4062+5A>G
- NM_001407874.1:c.3981+5A>G
- NM_001407875.1:c.3981+5A>G
- NM_001407879.1:c.3975+5A>G
- NM_001407881.1:c.3975+5A>G
- NM_001407882.1:c.3975+5A>G
- NM_001407884.1:c.3975+5A>G
- NM_001407885.1:c.3975+5A>G
- NM_001407886.1:c.3975+5A>G
- NM_001407887.1:c.3975+5A>G
- NM_001407889.1:c.3975+5A>G
- NM_001407894.1:c.3972+5A>G
- NM_001407895.1:c.3972+5A>G
- NM_001407896.1:c.3972+5A>G
- NM_001407897.1:c.3972+5A>G
- NM_001407898.1:c.3972+5A>G
- NM_001407899.1:c.3972+5A>G
- NM_001407900.1:c.3975+5A>G
- NM_001407902.1:c.3975+5A>G
- NM_001407904.1:c.3975+5A>G
- NM_001407906.1:c.3975+5A>G
- NM_001407907.1:c.3975+5A>G
- NM_001407908.1:c.3975+5A>G
- NM_001407909.1:c.3975+5A>G
- NM_001407910.1:c.3975+5A>G
- NM_001407915.1:c.3972+5A>G
- NM_001407916.1:c.3972+5A>G
- NM_001407917.1:c.3972+5A>G
- NM_001407918.1:c.3972+5A>G
- NM_001407919.1:c.4062+5A>G
- NM_001407920.1:c.3921+5A>G
- NM_001407921.1:c.3921+5A>G
- NM_001407922.1:c.3921+5A>G
- NM_001407923.1:c.3921+5A>G
- NM_001407924.1:c.3921+5A>G
- NM_001407925.1:c.3921+5A>G
- NM_001407926.1:c.3921+5A>G
- NM_001407927.1:c.3921+5A>G
- NM_001407928.1:c.3921+5A>G
- NM_001407929.1:c.3921+5A>G
- NM_001407930.1:c.3918+5A>G
- NM_001407931.1:c.3918+5A>G
- NM_001407932.1:c.3918+5A>G
- NM_001407933.1:c.3921+5A>G
- NM_001407934.1:c.3918+5A>G
- NM_001407935.1:c.3921+5A>G
- NM_001407936.1:c.3918+5A>G
- NM_001407937.1:c.4062+5A>G
- NM_001407938.1:c.4062+5A>G
- NM_001407939.1:c.4062+5A>G
- NM_001407940.1:c.4059+5A>G
- NM_001407941.1:c.4059+5A>G
- NM_001407942.1:c.4044+5A>G
- NM_001407943.1:c.4041+5A>G
- NM_001407944.1:c.4044+5A>G
- NM_001407945.1:c.4044+5A>G
- NM_001407946.1:c.3852+5A>G
- NM_001407947.1:c.3852+5A>G
- NM_001407948.1:c.3852+5A>G
- NM_001407949.1:c.3852+5A>G
- NM_001407950.1:c.3852+5A>G
- NM_001407951.1:c.3852+5A>G
- NM_001407952.1:c.3852+5A>G
- NM_001407953.1:c.3852+5A>G
- NM_001407954.1:c.3849+5A>G
- NM_001407955.1:c.3849+5A>G
- NM_001407956.1:c.3849+5A>G
- NM_001407957.1:c.3852+5A>G
- NM_001407958.1:c.3849+5A>G
- NM_001407959.1:c.3804+5A>G
- NM_001407960.1:c.3804+5A>G
- NM_001407962.1:c.3801+5A>G
- NM_001407963.1:c.3804+5A>G
- NM_001407964.1:c.4041+5A>G
- NM_001407965.1:c.3681+5A>G
- NM_001407966.1:c.3297+5A>G
- NM_001407967.1:c.3297+5A>G
- NM_001407968.1:c.1581+5A>G
- NM_001407969.1:c.1581+5A>G
- NM_001407970.1:c.876+5A>G
- NM_001407971.1:c.876+5A>G
- NM_001407972.1:c.873+5A>G
- NM_001407973.1:c.876+5A>G
- NM_001407974.1:c.876+5A>G
- NM_001407975.1:c.876+5A>G
- NM_001407976.1:c.876+5A>G
- NM_001407977.1:c.876+5A>G
- NM_001407978.1:c.876+5A>G
- NM_001407979.1:c.876+5A>G
- NM_001407980.1:c.876+5A>G
- NM_001407981.1:c.876+5A>G
- NM_001407982.1:c.876+5A>G
- NM_001407983.1:c.876+5A>G
- NM_001407984.1:c.873+5A>G
- NM_001407985.1:c.873+5A>G
- NM_001407986.1:c.873+5A>G
- NM_001407990.1:c.876+5A>G
- NM_001407991.1:c.873+5A>G
- NM_001407992.1:c.873+5A>G
- NM_001407993.1:c.876+5A>G
- NM_001408392.1:c.873+5A>G
- NM_001408396.1:c.873+5A>G
- NM_001408397.1:c.873+5A>G
- NM_001408398.1:c.873+5A>G
- NM_001408399.1:c.873+5A>G
- NM_001408400.1:c.873+5A>G
- NM_001408401.1:c.873+5A>G
- NM_001408402.1:c.873+5A>G
- NM_001408403.1:c.876+5A>G
- NM_001408404.1:c.876+5A>G
- NM_001408406.1:c.870+5A>G
- NM_001408407.1:c.873+5A>G
- NM_001408408.1:c.867+5A>G
- NM_001408409.1:c.798+5A>G
- NM_001408410.1:c.735+5A>G
- NM_001408411.1:c.798+5A>G
- NM_001408412.1:c.798+5A>G
- NM_001408413.1:c.795+5A>G
- NM_001408414.1:c.798+5A>G
- NM_001408415.1:c.798+5A>G
- NM_001408416.1:c.795+5A>G
- NM_001408418.1:c.759+5A>G
- NM_001408419.1:c.759+5A>G
- NM_001408420.1:c.759+5A>G
- NM_001408421.1:c.756+5A>G
- NM_001408422.1:c.759+5A>G
- NM_001408423.1:c.759+5A>G
- NM_001408424.1:c.756+5A>G
- NM_001408425.1:c.753+5A>G
- NM_001408426.1:c.753+5A>G
- NM_001408427.1:c.753+5A>G
- NM_001408428.1:c.753+5A>G
- NM_001408429.1:c.753+5A>G
- NM_001408430.1:c.753+5A>G
- NM_001408431.1:c.756+5A>G
- NM_001408432.1:c.750+5A>G
- NM_001408433.1:c.750+5A>G
- NM_001408434.1:c.750+5A>G
- NM_001408435.1:c.750+5A>G
- NM_001408436.1:c.753+5A>G
- NM_001408437.1:c.753+5A>G
- NM_001408438.1:c.753+5A>G
- NM_001408439.1:c.753+5A>G
- NM_001408440.1:c.753+5A>G
- NM_001408441.1:c.753+5A>G
- NM_001408442.1:c.753+5A>G
- NM_001408443.1:c.753+5A>G
- NM_001408444.1:c.753+5A>G
- NM_001408445.1:c.750+5A>G
- NM_001408446.1:c.750+5A>G
- NM_001408447.1:c.750+5A>G
- NM_001408448.1:c.750+5A>G
- NM_001408450.1:c.750+5A>G
- NM_001408451.1:c.741+5A>G
- NM_001408452.1:c.735+5A>G
- NM_001408453.1:c.735+5A>G
- NM_001408454.1:c.735+5A>G
- NM_001408455.1:c.735+5A>G
- NM_001408456.1:c.735+5A>G
- NM_001408457.1:c.735+5A>G
- NM_001408458.1:c.735+5A>G
- NM_001408459.1:c.735+5A>G
- NM_001408460.1:c.735+5A>G
- NM_001408461.1:c.735+5A>G
- NM_001408462.1:c.732+5A>G
- NM_001408463.1:c.732+5A>G
- NM_001408464.1:c.732+5A>G
- NM_001408465.1:c.732+5A>G
- NM_001408466.1:c.735+5A>G
- NM_001408467.1:c.735+5A>G
- NM_001408468.1:c.732+5A>G
- NM_001408469.1:c.735+5A>G
- NM_001408470.1:c.732+5A>G
- NM_001408472.1:c.876+5A>G
- NM_001408473.1:c.873+5A>G
- NM_001408474.1:c.675+5A>G
- NM_001408475.1:c.672+5A>G
- NM_001408476.1:c.675+5A>G
- NM_001408478.1:c.666+5A>G
- NM_001408479.1:c.666+5A>G
- NM_001408480.1:c.666+5A>G
- NM_001408481.1:c.666+5A>G
- NM_001408482.1:c.666+5A>G
- NM_001408483.1:c.666+5A>G
- NM_001408484.1:c.666+5A>G
- NM_001408485.1:c.666+5A>G
- NM_001408489.1:c.666+5A>G
- NM_001408490.1:c.663+5A>G
- NM_001408491.1:c.663+5A>G
- NM_001408492.1:c.666+5A>G
- NM_001408493.1:c.663+5A>G
- NM_001408494.1:c.636+5A>G
- NM_001408495.1:c.633+5A>G
- NM_001408496.1:c.612+5A>G
- NM_001408497.1:c.612+5A>G
- NM_001408498.1:c.612+5A>G
- NM_001408499.1:c.612+5A>G
- NM_001408500.1:c.612+5A>G
- NM_001408501.1:c.612+5A>G
- NM_001408502.1:c.543+5A>G
- NM_001408503.1:c.609+5A>G
- NM_001408504.1:c.609+5A>G
- NM_001408505.1:c.609+5A>G
- NM_001408506.1:c.549+5A>G
- NM_001408507.1:c.549+5A>G
- NM_001408508.1:c.540+5A>G
- NM_001408509.1:c.540+5A>G
- NM_001408510.1:c.495+5A>G
- NM_001408511.1:c.492+5A>G
- NM_001408512.1:c.372+5A>G
- NM_001408513.1:c.666+5A>G
- NM_001408514.1:c.666+5A>G
- NM_007294.4:c.4185+5A>GMANE SELECT
- NM_007297.4:c.4044+5A>G
- NM_007298.4:c.876+5A>G
- NM_007299.4:c.876+5A>G
- NM_007300.4:c.4185+5A>G
- LRG_292t1:c.4185+5A>G
- LRG_292:g.127045A>G
- NC_000017.10:g.41242956T>C
- NM_007294.3:c.4185+5A>G
This HGVS expression did not pass validation- Links:
- dbSNP: rs766330646
- NCBI 1000 Genomes Browser:
- rs766330646
- Molecular consequence:
- NM_001407571.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407581.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407582.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407583.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407585.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407587.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407590.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407591.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407593.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407594.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407596.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407597.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407598.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407602.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407603.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407605.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407610.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407611.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407612.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407613.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407614.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407615.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407616.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407617.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407618.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407619.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407620.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407621.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407622.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407623.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407624.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407625.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407626.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407627.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407628.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407629.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407630.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407631.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407632.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407633.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407634.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407635.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407636.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407637.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407638.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407639.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407640.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407641.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407642.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407644.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407645.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407646.1:c.4176+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407647.1:c.4176+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407648.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407649.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407652.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407653.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407654.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407655.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407656.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407657.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407658.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407659.1:c.4104+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407660.1:c.4104+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407661.1:c.4104+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407662.1:c.4104+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407663.1:c.4107+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407664.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407665.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407666.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407667.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407668.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407669.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407670.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407671.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407672.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407673.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407674.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407675.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407676.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407677.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407678.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407679.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407680.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407681.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407682.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407683.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407684.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407685.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407686.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407687.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407688.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407689.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407690.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407691.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407692.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407694.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407695.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407696.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407697.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407698.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407724.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407725.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407726.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407727.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407728.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407729.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407730.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407731.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407732.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407733.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407734.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407735.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407736.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407737.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407738.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407739.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407740.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407741.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407742.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407743.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407744.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407745.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407746.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407747.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407748.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407749.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407750.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407751.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407752.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407838.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407839.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407841.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407842.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407843.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407844.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407845.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407846.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407847.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407848.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407849.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407850.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407851.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407852.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407853.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407854.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407858.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407859.1:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407860.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407861.1:c.4182+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407862.1:c.3984+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407863.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407874.1:c.3981+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407875.1:c.3981+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407879.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407881.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407882.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407884.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407885.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407886.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407887.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407889.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407894.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407895.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407896.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407897.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407898.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407899.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407900.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407902.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407904.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407906.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407907.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407908.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407909.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407910.1:c.3975+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407915.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407916.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407917.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407918.1:c.3972+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407919.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407920.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407921.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407922.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407923.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407924.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407925.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407926.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407927.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407928.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407929.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407930.1:c.3918+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407931.1:c.3918+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407932.1:c.3918+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407933.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407934.1:c.3918+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407935.1:c.3921+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407936.1:c.3918+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407937.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407938.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407939.1:c.4062+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407940.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407941.1:c.4059+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407942.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407943.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407944.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407945.1:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407946.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407947.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407948.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407949.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407950.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407951.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407952.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407953.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407954.1:c.3849+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407955.1:c.3849+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407956.1:c.3849+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407957.1:c.3852+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407958.1:c.3849+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407959.1:c.3804+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407960.1:c.3804+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407962.1:c.3801+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407963.1:c.3804+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407964.1:c.4041+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407965.1:c.3681+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407966.1:c.3297+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407967.1:c.3297+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407968.1:c.1581+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407969.1:c.1581+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407970.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407971.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407972.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407973.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407974.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407975.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407976.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407977.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407978.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407979.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407980.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407981.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407982.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407983.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407984.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407985.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407986.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407990.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407991.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407992.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001407993.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408392.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408396.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408397.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408398.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408399.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408400.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408401.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408402.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408403.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408404.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408406.1:c.870+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408407.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408408.1:c.867+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408409.1:c.798+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408410.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408411.1:c.798+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408412.1:c.798+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408413.1:c.795+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408414.1:c.798+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408415.1:c.798+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408416.1:c.795+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408418.1:c.759+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408419.1:c.759+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408420.1:c.759+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408421.1:c.756+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408422.1:c.759+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408423.1:c.759+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408424.1:c.756+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408425.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408426.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408427.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408428.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408429.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408430.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408431.1:c.756+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408432.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408433.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408434.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408435.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408436.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408437.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408438.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408439.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408440.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408441.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408442.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408443.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408444.1:c.753+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408445.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408446.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408447.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408448.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408450.1:c.750+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408451.1:c.741+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408452.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408453.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408454.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408455.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408456.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408457.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408458.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408459.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408460.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408461.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408462.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408463.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408464.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408465.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408466.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408467.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408468.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408469.1:c.735+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408470.1:c.732+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408472.1:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408473.1:c.873+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408474.1:c.675+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408475.1:c.672+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408476.1:c.675+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408478.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408479.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408480.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408481.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408482.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408483.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408484.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408485.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408489.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408490.1:c.663+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408491.1:c.663+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408492.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408493.1:c.663+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408494.1:c.636+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408495.1:c.633+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408496.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408497.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408498.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408499.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408500.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408501.1:c.612+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408502.1:c.543+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408503.1:c.609+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408504.1:c.609+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408505.1:c.609+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408506.1:c.549+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408507.1:c.549+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408508.1:c.540+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408509.1:c.540+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408510.1:c.495+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408511.1:c.492+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408512.1:c.372+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408513.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_001408514.1:c.666+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007294.4:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007297.4:c.4044+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007298.4:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007299.4:c.876+5A>G - intron variant - [Sequence Ontology: SO:0001627]
- NM_007300.4:c.4185+5A>G - intron variant - [Sequence Ontology: SO:0001627]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000888906 | Quest Diagnostics Nichols Institute San Juan Capistrano | criteria provided, single submitter (Quest Diagnostics criteria) | Uncertain significance (Apr 21, 2018) | germline | clinical testing | |
SCV000983297 | GeneDx | criteria provided, single submitter (GeneDx Variant Classification (06012015)) | Likely benign (Mar 30, 2018) | germline | clinical testing |
Summary from all submissions
Ethnicity | Origin | Affected | Individuals | Families | Chromosomes tested | Number Tested | Family history | Method |
---|---|---|---|---|---|---|---|---|
not provided | germline | yes | not provided | not provided | not provided | not provided | not provided | clinical testing |
not provided | germline | unknown | not provided | not provided | not provided | not provided | not provided | clinical testing |
Citations
PubMed
A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.
Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.
Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.
- PMID:
- 26467025
- PMCID:
- PMC4737317
Details of each submission
From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV000888906.2
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | PubMed (1) |
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | unknown | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
From GeneDx, SCV000983297.1
# | Ethnicity | Individuals | Chromosomes Tested | Family History | Method | Citations |
---|---|---|---|---|---|---|
1 | not provided | not provided | not provided | not provided | clinical testing | not provided |
Description
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
# | Sample | Method | Observation | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences | |
1 | germline | yes | not provided | not provided | not provided | not provided | not provided | not provided | not provided |
Last Updated: Feb 28, 2024