ClinVar Miner

List of variants in gene COL4A1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_001845.5(COL4A1):c.*1404T>C rs56406633
NM_001845.5(COL4A1):c.3326-7dupT rs139122216
NM_001845.6(COL4A1):c.*1014C>T rs139916479
NM_001845.6(COL4A1):c.*1099G>A rs193065628
NM_001845.6(COL4A1):c.*176A>G rs11545877
NM_001845.6(COL4A1):c.*265A>G rs555157539
NM_001845.6(COL4A1):c.*609T>C rs189966143
NM_001845.6(COL4A1):c.*766G>A rs371130027
NM_001845.6(COL4A1):c.*975A>C rs28362515
NM_001845.6(COL4A1):c.1000-13C>G rs115358624
NM_001845.6(COL4A1):c.1000-5T>G rs75711155
NM_001845.6(COL4A1):c.1466-6C>T rs183563055
NM_001845.6(COL4A1):c.161C>T (p.Pro54Leu) rs34004222
NM_001845.6(COL4A1):c.1673C>T (p.Ala558Val) rs200252122
NM_001845.6(COL4A1):c.2103C>T (p.Asp701=) rs561116319
NM_001845.6(COL4A1):c.2313G>A (p.Ala771=) rs781701888
NM_001845.6(COL4A1):c.2624C>G (p.Pro875Arg) rs201964644
NM_001845.6(COL4A1):c.2627-4dup rs1555303159
NM_001845.6(COL4A1):c.2647G>A (p.Val883Ile) rs41275090
NM_001845.6(COL4A1):c.2811C>T (p.Ser937=) rs765239658
NM_001845.6(COL4A1):c.2869+6T>C rs557198622
NM_001845.6(COL4A1):c.2955G>C (p.Gln985His) rs145018661
NM_001845.6(COL4A1):c.2968+4C>T rs1555303033
NM_001845.6(COL4A1):c.3198+10G>A rs202002553
NM_001845.6(COL4A1):c.3285C>T (p.Ser1095=) rs267603751
NM_001845.6(COL4A1):c.3288A>G (p.Pro1096=) rs2305082
NM_001845.6(COL4A1):c.329T>C (p.Ile110Thr) rs138269346
NM_001845.6(COL4A1):c.3506-7C>G rs377592935
NM_001845.6(COL4A1):c.3634A>T (p.Met1212Leu) rs199557190
NM_001845.6(COL4A1):c.3776C>G (p.Pro1259Arg) rs146329532
NM_001845.6(COL4A1):c.3877-8G>A rs370539477
NM_001845.6(COL4A1):c.393G>A (p.Glu131=) rs34458255
NM_001845.6(COL4A1):c.3949+10C>T rs188122235
NM_001845.6(COL4A1):c.3972C>T (p.Leu1324=) rs535848796
NM_001845.6(COL4A1):c.4005C>T (p.Gly1335=) rs140722653
NM_001845.6(COL4A1):c.4010C>T (p.Pro1337Leu) rs189728415
NM_001845.6(COL4A1):c.4056C>T (p.Tyr1352=) rs140210015
NM_001845.6(COL4A1):c.405C>T (p.Leu135=) rs138888319
NM_001845.6(COL4A1):c.4150+3G>A rs545498227
NM_001845.6(COL4A1):c.4229T>C (p.Met1410Thr) rs200734000
NM_001845.6(COL4A1):c.4250-12C>T rs202055679
NM_001845.6(COL4A1):c.4441C>T (p.Arg1481Trp) rs199586038
NM_001845.6(COL4A1):c.4640+3G>T rs770167198
NM_001845.6(COL4A1):c.4640+8G>A rs117566874
NM_001845.6(COL4A1):c.4658C>T (p.Ala1553Val) rs201150281
NM_001845.6(COL4A1):c.4797G>A (p.Ala1599=) rs146638269
NM_001845.6(COL4A1):c.4803C>T (p.Pro1601=) rs190097900
NM_001845.6(COL4A1):c.4941G>A (p.Pro1647=) rs115834242
NM_001845.6(COL4A1):c.501C>T (p.Pro167=) rs16975612
NM_001845.6(COL4A1):c.651+4_651+5insCAC rs760194800
NM_001845.6(COL4A1):c.690C>T (p.Asp230=) rs149688210
NM_001845.6(COL4A1):c.708C>G (p.Val236=) rs139523466
NM_001845.6(COL4A1):c.781-12G>A rs202198648
NM_001845.6(COL4A1):c.807+3C>T rs192723236
NM_001845.6(COL4A1):c.904-9C>T rs201481886
NM_001845.6(COL4A1):c.994G>C (p.Gly332Arg) rs150182714

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.