ClinVar Miner

List of variants in gene COL12A1 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP
NM_004370.6(COL12A1):c.1551A>G (p.Thr517=) rs34767467
NM_004370.6(COL12A1):c.1892-8_1892-6del rs199713791
NM_004370.6(COL12A1):c.1897G>T (p.Val633Phe) rs200315815
NM_004370.6(COL12A1):c.2007G>A (p.Ala669=) rs77790445
NM_004370.6(COL12A1):c.2086T>C (p.Leu696=) rs116691242
NM_004370.6(COL12A1):c.2275C>T (p.Pro759Ser) rs141517088
NM_004370.6(COL12A1):c.2481G>A (p.Thr827=) rs35170847
NM_004370.6(COL12A1):c.2772T>C (p.Tyr924=) rs35429515
NM_004370.6(COL12A1):c.2965G>A (p.Gly989Arg) rs139332405
NM_004370.6(COL12A1):c.3630C>T (p.Ile1210=) rs572531941
NM_004370.6(COL12A1):c.3651C>T (p.Thr1217=) rs140319205
NM_004370.6(COL12A1):c.4001-10G>A rs73749974
NM_004370.6(COL12A1):c.4186C>A (p.Arg1396=) rs115511838
NM_004370.6(COL12A1):c.4245T>C (p.Tyr1415=) rs34830422
NM_004370.6(COL12A1):c.4876T>G (p.Ser1626Ala) rs77654847
NM_004370.6(COL12A1):c.4917C>T (p.Asp1639=) rs80102965
NM_004370.6(COL12A1):c.5133C>T (p.Phe1711=) rs180961776
NM_004370.6(COL12A1):c.5225G>A (p.Arg1742His) rs79830915
NM_004370.6(COL12A1):c.5508G>A (p.Thr1836=) rs77425231
NM_004370.6(COL12A1):c.5727C>T (p.Tyr1909=) rs146146364
NM_004370.6(COL12A1):c.5874A>G (p.Pro1958=) rs186035636
NM_004370.6(COL12A1):c.6062G>A (p.Arg2021Gln) rs34438461
NM_004370.6(COL12A1):c.6198A>C (p.Pro2066=) rs34619869
NM_004370.6(COL12A1):c.626A>C (p.Lys209Thr) rs75535959
NM_004370.6(COL12A1):c.6281C>A (p.Thr2094Asn) rs201567848
NM_004370.6(COL12A1):c.6345A>G (p.Gly2115=) rs553575841
NM_004370.6(COL12A1):c.6444A>T (p.Ile2148=) rs36002196
NM_004370.6(COL12A1):c.6479A>T (p.Glu2160Val) rs35523808
NM_004370.6(COL12A1):c.6590C>T (p.Thr2197Ile) rs117038107
NM_004370.6(COL12A1):c.6848G>A (p.Gly2283Glu) rs77094372
NM_004370.6(COL12A1):c.7299G>T (p.Thr2433=) rs35551395
NM_004370.6(COL12A1):c.7786A>G (p.Ile2596Val) rs35710072
NM_004370.6(COL12A1):c.8179-10A>G rs142509363
NM_004370.6(COL12A1):c.8237T>C (p.Val2746Ala) rs34369939
NM_004370.6(COL12A1):c.834T>G (p.Ala278=) rs16886258
NM_004370.6(COL12A1):c.8421C>T (p.Arg2807=) rs371949188
NM_004370.6(COL12A1):c.8565A>G (p.Pro2855=) rs202239067
NM_004370.6(COL12A1):c.8622A>G (p.Pro2874=) rs368321891
NM_004370.6(COL12A1):c.8925A>G (p.Gly2975=) rs190820180
NM_004370.6(COL12A1):c.8970T>C (p.Gly2990=) rs190501064
NM_004370.6(COL12A1):c.8980T>C (p.Ser2994Pro) rs34846477
NM_004370.6(COL12A1):c.9083G>A (p.Arg3028His) rs41266761
NM_004370.6(COL12A1):c.9162C>T (p.Tyr3054=) rs35292916

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.