ClinVar Miner

List of variants in gene COL4A1 reported as uncertain significance for Brain small vessel disease with hemorrhage

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP
NM_001845.6(COL4A1):c.*1039A>G rs776016334
NM_001845.6(COL4A1):c.*137G>A rs886049956
NM_001845.6(COL4A1):c.*477G>T rs886049955
NM_001845.6(COL4A1):c.*510A>G rs886049954
NM_001845.6(COL4A1):c.*531T>A rs886049953
NM_001845.6(COL4A1):c.*634_*635AT[8] rs886049952
NM_001845.6(COL4A1):c.*6C>G rs762512053
NM_001845.6(COL4A1):c.*887del rs886049951
NM_001845.6(COL4A1):c.-20G>T rs886049965
NM_001845.6(COL4A1):c.-71C>G rs867117624
NM_001845.6(COL4A1):c.1385A>G (p.Gln462Arg) rs750386918
NM_001845.6(COL4A1):c.1588C>T (p.Pro530Ser) rs145172612
NM_001845.6(COL4A1):c.1858G>C (p.Ala620Pro) rs372803920
NM_001845.6(COL4A1):c.2007C>T (p.Pro669=) rs145645897
NM_001845.6(COL4A1):c.2095+7C>G rs886049961
NM_001845.6(COL4A1):c.2126C>T (p.Pro709Leu) rs150129180
NM_001845.6(COL4A1):c.2160C>T (p.Gly720=) rs781133776
NM_001845.6(COL4A1):c.2262C>T (p.Pro754=) rs750538499
NM_001845.6(COL4A1):c.2344+11G>A rs886049960
NM_001845.6(COL4A1):c.2706G>A (p.Pro902=) rs754208625
NM_001845.6(COL4A1):c.2732C>T (p.Pro911Leu) rs778143775
NM_001845.6(COL4A1):c.280-12C>T rs200121908
NM_001845.6(COL4A1):c.2968+12A>G rs752476229
NM_001845.6(COL4A1):c.3018T>G (p.Leu1006=) rs886049959
NM_001845.6(COL4A1):c.3164C>T (p.Pro1055Leu) rs375787099
NM_001845.6(COL4A1):c.3241A>G (p.Lys1081Glu) rs886049958
NM_001845.6(COL4A1):c.3431C>G (p.Thr1144Arg) rs769021800
NM_001845.6(COL4A1):c.3557-14T>C rs886049957
NM_001845.6(COL4A1):c.3742+14G>A rs377503687
NM_001845.6(COL4A1):c.380G>T (p.Gly127Val) rs886049963
NM_001845.6(COL4A1):c.388-11T>C rs201801894
NM_001845.6(COL4A1):c.4021+14T>A rs755709828
NM_001845.6(COL4A1):c.4038T>C (p.Pro1346=) rs372556002
NM_001845.6(COL4A1):c.4271C>T (p.Pro1424Leu) rs760889798
NM_001845.6(COL4A1):c.4442G>A (p.Arg1481Gln) rs376607450
NM_001845.6(COL4A1):c.553-8C>T rs199534388
NM_001845.6(COL4A1):c.766A>G (p.Thr256Ala) rs886049962
NM_001845.6(COL4A1):c.82A>G (p.Lys28Glu) rs886049964

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.