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Links from Gene

Items: 6

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr15:32964740-32988830
GRCh38:
Chr15:32672539-32696629
SCG5, GREM1, LOC105370757, ARHGAP11A-SCG5Familial colorectal cancerUncertain significance
(Jan 11, 2018)
criteria provided, single submitterVCV000476577
2.
Likely benign
(Jun 1, 2012)
criteria provided, single submitterVCV000424722
3.
GRCh37:
Chr15:32983953
GRCh38:
Chr15:32691752
SCG5, ARHGAP11A-SCG5R178*, R177*, R591*Hereditary Mixed PolyposisUncertain significance
(Aug 13, 2015)
criteria provided, single submitterVCV000374976
4.
GRCh37:
Chr15:32920998
GRCh38:
Chr15:32628797
ARHGAP11A, ARHGAP11A-SCG5R311I, R122Ino interpretation for the single variantno interpretation for the single variantVCV000242613
5.
GRCh37:
Chr15:32927988
GRCh38:
Chr15:32635787
ARHGAP11A, ARHGAP11A-SCG5S452C, S263Cno interpretation for the single variantno interpretation for the single variantVCV000242612
6.
GRCh37:
Chr15:32929344-32929345
GRCh38:
Chr15:32637143-32637144
ARHGAP11A, ARHGAP11A-SCG5Inborn genetic diseasesLikely pathogenic
(Apr 18, 2014)
criteria provided, single submitterVCV000225089
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