SNP for Gene (Select 282618) - SNP

Links from Gene

Items: 1 to 20 of 1291

<< First< Prev

Page of 65

Next >Last >>

Select item 14914178111.

rs1491417811 has merged into rs10638174 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGAGAGAGAGAGAGA>-,GAGA,GAGAGA,GAGAGAGA,GAGAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
Chromosome:: 19:39294564 (GRCh38)
19:39785204 (GRCh37)
Canonical SPDI:: NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:39294548:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
Gene:: IFNL1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGAGAGAGAGAGA=0./0 (ALFA)
-=0.125/1 (KOREAN)
AGAG=0.2544/1274 (1000Genomes)
HGVS:: NC_000019.10:g.39294550GA[7], NC_000019.10:g.39294550GA[9], NC_000019.10:g.39294550GA[10], NC_000019.10:g.39294550GA[11], NC_000019.10:g.39294550GA[12], NC_000019.10:g.39294550GA[13], NC_000019.10:g.39294550GA[14], NC_000019.10:g.39294550GA[15], NC_000019.10:g.39294550GA[17], NC_000019.10:g.39294550GA[18], NC_000019.10:g.39294550GA[19], NC_000019.10:g.39294550GA[20], NC_000019.10:g.39294550GA[21], NC_000019.10:g.39294550GA[22], NC_000019.10:g.39294550GA[23], NC_000019.10:g.39294550GA[24], NC_000019.10:g.39294550GA[25], NC_000019.10:g.39294550GA[26], NC_000019.10:g.39294550GA[27], NC_000019.10:g.39294550GA[30], NC_000019.9:g.39785190GA[7], NC_000019.9:g.39785190GA[9], NC_000019.9:g.39785190GA[10], NC_000019.9:g.39785190GA[11], NC_000019.9:g.39785190GA[12], NC_000019.9:g.39785190GA[13], NC_000019.9:g.39785190GA[14], NC_000019.9:g.39785190GA[15], NC_000019.9:g.39785190GA[17], NC_000019.9:g.39785190GA[18], NC_000019.9:g.39785190GA[19], NC_000019.9:g.39785190GA[20], NC_000019.9:g.39785190GA[21], NC_000019.9:g.39785190GA[22], NC_000019.9:g.39785190GA[23], NC_000019.9:g.39785190GA[24], NC_000019.9:g.39785190GA[25], NC_000019.9:g.39785190GA[26], NC_000019.9:g.39785190GA[27], NC_000019.9:g.39785190GA[30], NW_025791808.1:g.74932GA[7], NW_025791808.1:g.74932GA[9], NW_025791808.1:g.74932GA[10], NW_025791808.1:g.74932GA[11], NW_025791808.1:g.74932GA[12], NW_025791808.1:g.74932GA[13], NW_025791808.1:g.74932GA[14], NW_025791808.1:g.74932GA[15], NW_025791808.1:g.74932GA[17], NW_025791808.1:g.74932GA[18], NW_025791808.1:g.74932GA[19], NW_025791808.1:g.74932GA[20], NW_025791808.1:g.74932GA[21], NW_025791808.1:g.74932GA[22], NW_025791808.1:g.74932GA[23], NW_025791808.1:g.74932GA[24], NW_025791808.1:g.74932GA[25], NW_025791808.1:g.74932GA[26], NW_025791808.1:g.74932GA[27], NW_025791808.1:g.74932GA[30]

Select item 14907100032.

rs1490710003 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:39297539 (GRCh38)
19:39788179 (GRCh37)
Canonical SPDI:: NC_000019.10:39297538:C:G,NC_000019.10:39297538:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.39297539C>G, NC_000019.10:g.39297539C>T, NC_000019.9:g.39788179C>G, NC_000019.9:g.39788179C>T, NW_025791808.1:g.77921C>G, NW_025791808.1:g.77921C>T

Select item 14905953253.

rs1490595325 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:39296218 (GRCh38)
19:39786858 (GRCh37)
Canonical SPDI:: NC_000019.10:39296217:G:A
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.39296218G>A, NC_000019.9:g.39786858G>A, NW_025791808.1:g.76600G>A

Select item 14905703234.

rs1490570323 has merged into rs59725017 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:39297322 (GRCh38)
19:39787962 (GRCh37)
Canonical SPDI:: NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:39297310:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTT=0.225/9 (GENOME_DK)
HGVS:: NC_000019.10:g.39297322_39297336del, NC_000019.10:g.39297323_39297336del, NC_000019.10:g.39297324_39297336del, NC_000019.10:g.39297325_39297336del, NC_000019.10:g.39297326_39297336del, NC_000019.10:g.39297327_39297336del, NC_000019.10:g.39297328_39297336del, NC_000019.10:g.39297329_39297336del, NC_000019.10:g.39297330_39297336del, NC_000019.10:g.39297331_39297336del, NC_000019.10:g.39297332_39297336del, NC_000019.10:g.39297333_39297336del, NC_000019.10:g.39297334_39297336del, NC_000019.10:g.39297335_39297336del, NC_000019.10:g.39297336del, NC_000019.10:g.39297336dup, NC_000019.10:g.39297335_39297336dup, NC_000019.10:g.39297334_39297336dup, NC_000019.10:g.39297333_39297336dup, NC_000019.10:g.39297332_39297336dup, NC_000019.10:g.39297331_39297336dup, NC_000019.10:g.39297329_39297336dup, NC_000019.9:g.39787962_39787976del, NC_000019.9:g.39787963_39787976del, NC_000019.9:g.39787964_39787976del, NC_000019.9:g.39787965_39787976del, NC_000019.9:g.39787966_39787976del, NC_000019.9:g.39787967_39787976del, NC_000019.9:g.39787968_39787976del, NC_000019.9:g.39787969_39787976del, NC_000019.9:g.39787970_39787976del, NC_000019.9:g.39787971_39787976del, NC_000019.9:g.39787972_39787976del, NC_000019.9:g.39787973_39787976del, NC_000019.9:g.39787974_39787976del, NC_000019.9:g.39787975_39787976del, NC_000019.9:g.39787976del, NC_000019.9:g.39787976dup, NC_000019.9:g.39787975_39787976dup, NC_000019.9:g.39787974_39787976dup, NC_000019.9:g.39787973_39787976dup, NC_000019.9:g.39787972_39787976dup, NC_000019.9:g.39787971_39787976dup, NC_000019.9:g.39787969_39787976dup, NW_025791808.1:g.77704_77718del, NW_025791808.1:g.77705_77718del, NW_025791808.1:g.77706_77718del, NW_025791808.1:g.77707_77718del, NW_025791808.1:g.77708_77718del, NW_025791808.1:g.77709_77718del, NW_025791808.1:g.77710_77718del, NW_025791808.1:g.77711_77718del, NW_025791808.1:g.77712_77718del, NW_025791808.1:g.77713_77718del, NW_025791808.1:g.77714_77718del, NW_025791808.1:g.77715_77718del, NW_025791808.1:g.77716_77718del, NW_025791808.1:g.77717_77718del, NW_025791808.1:g.77718del, NW_025791808.1:g.77718dup, NW_025791808.1:g.77717_77718dup, NW_025791808.1:g.77716_77718dup, NW_025791808.1:g.77715_77718dup, NW_025791808.1:g.77714_77718dup, NW_025791808.1:g.77713_77718dup, NW_025791808.1:g.77711_77718dup

Select item 14902254775.

rs1490225477 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:39297827 (GRCh38)
19:39788467 (GRCh37)
Canonical SPDI:: NC_000019.10:39297826:T:A
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.39297827T>A, NC_000019.9:g.39788467T>A, NW_025791808.1:g.78209T>A

Select item 14893524766.

rs1489352476 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:39295584 (GRCh38)
19:39786224 (GRCh37)
Canonical SPDI:: NC_000019.10:39295583:T:C
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.39295584T>C, NC_000019.9:g.39786224T>C, NW_025791808.1:g.75966T>C

Select item 14891250387.

rs1489125038 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:39294496 (GRCh38)
19:39785136 (GRCh37)
Canonical SPDI:: NC_000019.10:39294495:T:C
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000016/2 (GnomAD)
HGVS:: NC_000019.10:g.39294496T>C, NC_000019.9:g.39785136T>C, NW_025791808.1:g.74878T>C

Select item 14890561078.

rs1489056107 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:39295850 (GRCh38)
19:39786490 (GRCh37)
Canonical SPDI:: NC_000019.10:39295849:C:G
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.39295850C>G, NC_000019.9:g.39786490C>G, NW_025791808.1:g.76232C>G

Select item 14888411959.

rs1488841195 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39297755 (GRCh38)
19:39788395 (GRCh37)
Canonical SPDI:: NC_000019.10:39297754:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.39297755C>T, NC_000019.9:g.39788395C>T, NW_025791808.1:g.78137C>T

Select item 148675966810.

rs1486759668 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:39296590 (GRCh38)
19:39787230 (GRCh37)
Canonical SPDI:: NC_000019.10:39296589:T:G
Gene:: IFNL1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.39296590T>G, NC_000019.9:g.39787230T>G, NW_025791808.1:g.76972T>G, NM_172140.2:c.169T>G, NM_172140.1:c.169T>G, NP_742152.1:p.Leu57Val

Select item 148500533811.

rs1485005338 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:39297388 (GRCh38)
19:39788028 (GRCh37)
Canonical SPDI:: NC_000019.10:39297387:G:A
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000034/9 (TOPMED)
A=0.000107/14 (GnomAD)
HGVS:: NC_000019.10:g.39297388G>A, NC_000019.9:g.39788028G>A, NW_025791808.1:g.77770G>A

Select item 148480749912.

rs1484807499 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 19:39298305 (GRCh38)
19:39788945 (GRCh37)
Canonical SPDI:: NC_000019.10:39298304:CCC:CC
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.39298307del, NC_000019.9:g.39788947del, NW_025791808.1:g.78689del

Select item 148435283113.

rs1484352831 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39295562 (GRCh38)
19:39786202 (GRCh37)
Canonical SPDI:: NC_000019.10:39295561:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000162/3 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000079/11 (GnomAD)
T=0.00067/3 (Estonian)
HGVS:: NC_000019.10:g.39295562C>T, NC_000019.9:g.39786202C>T, NW_025791808.1:g.75944C>T

Select item 148338518314.

rs1483385183 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:39295192 (GRCh38)
19:39785832 (GRCh37)
Canonical SPDI:: NC_000019.10:39295191:A:G
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.39295192A>G, NC_000019.9:g.39785832A>G, NW_025791808.1:g.75574A>G

Select item 148215561715.

rs1482155617 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:39298742 (GRCh38)
19:39789382 (GRCh37)
Canonical SPDI:: NC_000019.10:39298741:G:C
Gene:: IFNL1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.39298742G>C, NC_000019.9:g.39789382G>C, NW_025791808.1:g.79124G>C

Select item 148130885516.

rs1481308855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 19:39296908 (GRCh38)
19:39787548 (GRCh37)
Canonical SPDI:: NC_000019.10:39296907:A:C,NC_000019.10:39296907:A:T
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
C=0.001092/2 (Korea1K)
HGVS:: NC_000019.10:g.39296908A>C, NC_000019.10:g.39296908A>T, NC_000019.9:g.39787548A>C, NC_000019.9:g.39787548A>T, NW_025791808.1:g.77290A>C, NW_025791808.1:g.77290A>T

Select item 148083465017.

rs1480834650 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:39294325 (GRCh38)
19:39784965 (GRCh37)
Canonical SPDI:: NC_000019.10:39294324:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.39294325G>A, NC_000019.9:g.39784965G>A, NW_025791808.1:g.74707G>A

Select item 148081507118.

rs1480815071 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39297526 (GRCh38)
19:39788166 (GRCh37)
Canonical SPDI:: NC_000019.10:39297525:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000019.10:g.39297526C>T, NC_000019.9:g.39788166C>T, NW_025791808.1:g.77908C>T

Select item 148036407419.

rs1480364074 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:39295485 (GRCh38)
19:39786125 (GRCh37)
Canonical SPDI:: NC_000019.10:39295484:C:G,NC_000019.10:39295484:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.39295485C>G, NC_000019.10:g.39295485C>T, NC_000019.9:g.39786125C>G, NC_000019.9:g.39786125C>T, NW_025791808.1:g.75867C>G, NW_025791808.1:g.75867C>T

Select item 148018784420.

rs1480187844 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39299004 (GRCh38)
19:39789644 (GRCh37)
Canonical SPDI:: NC_000019.10:39299003:C:T
Gene:: IFNL1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.39299004C>T, NC_000019.9:g.39789644C>T, NW_025791808.1:g.79386C>T

<< First< Prev

Page of 65

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1291

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity