ClinVar Miner

List of variants in gene INF2 reported by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP
NM_022489.3(INF2):c.105C>T (p.Pro35=) rs4983530
NM_022489.3(INF2):c.1736-18C>T rs199612826
NM_022489.3(INF2):c.1949+16A>G rs11850821
NM_022489.3(INF2):c.2310+8delA rs3840006
NM_022489.3(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.3(INF2):c.2458C>T (p.Arg820Trp) rs79327775
NM_022489.3(INF2):c.2571C>T (p.Ser857=) rs62640005
NM_022489.3(INF2):c.2630G>A (p.Arg877Gln) rs142678449
NM_022489.3(INF2):c.2640T>C (p.Asp880=) rs10133301
NM_022489.3(INF2):c.2775+15C>T rs73347508
NM_022489.3(INF2):c.3066T>C (p.Asp1022=) rs4983535
NM_022489.3(INF2):c.3069C>T (p.Pro1023=) rs75382114
NM_022489.3(INF2):c.3108T>C (p.Leu1036=) rs186075307
NM_022489.3(INF2):c.3153C>T (p.Asp1051=) rs117457867
NM_022489.3(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.3(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.3(INF2):c.3286C>T (p.Pro1096Ser) rs34251364
NM_022489.3(INF2):c.3404C>T (p.Thr1135Met) rs3803311
NM_022489.3(INF2):c.3747G>A (p.Gln1249=) rs149939482
NM_022489.3(INF2):c.391+17G>A rs4074531
NM_022489.3(INF2):c.391+18A>T rs115458897
NM_022489.3(INF2):c.391+6C>T rs75115369
NM_022489.3(INF2):c.42G>A (p.Leu14=) rs62638758
NM_022489.3(INF2):c.489C>T (p.Asp163=) rs769080446
NM_022489.3(INF2):c.624C>T (p.Pro208=) rs750610272
NM_022489.3(INF2):c.843+16C>T rs118017785
NM_022489.3(INF2):c.879G>A (p.Ser293=) rs184709736

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.