ClinVar Miner

List of variants in gene TAF1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004606.5(TAF1):c.830A>T (p.Gln277Leu) rs150416138 0.00079
NM_004606.5(TAF1):c.3228-6T>C rs376706489 0.00069
NM_004606.5(TAF1):c.2688G>A (p.Glu896=) rs148921433 0.00059
NM_004606.5(TAF1):c.891C>T (p.Tyr297=) rs149605307 0.00045
NM_004606.5(TAF1):c.297T>C (p.Asp99=) rs144106353 0.00036
NM_004606.5(TAF1):c.4698G>A (p.Arg1566=) rs148007434 0.00033
NM_004606.5(TAF1):c.4754-4A>G rs370696191 0.00029
NM_004606.5(TAF1):c.4155G>A (p.Thr1385=) rs202158967 0.00009
NM_004606.5(TAF1):c.3090G>A (p.Val1030=) rs745568855 0.00008
NM_004606.5(TAF1):c.5230C>T (p.Leu1744=) rs139893377 0.00006
NM_004606.5(TAF1):c.1666-8A>G rs374932400 0.00003
NM_004606.5(TAF1):c.4948T>C (p.Leu1650=) rs779320845 0.00003
NM_004606.5(TAF1):c.633A>G (p.Pro211=) rs773107206 0.00001
NM_004606.4(TAF1):c.22C>T (p.Leu8=)
NM_004606.5(TAF1):c.*424C>T
NM_004606.5(TAF1):c.-7C>T rs1437283873
NM_004606.5(TAF1):c.1086G>A (p.Gly362=)
NM_004606.5(TAF1):c.1170G>A (p.Glu390=)
NM_004606.5(TAF1):c.145T>C (p.Leu49=)
NM_004606.5(TAF1):c.1480C>T (p.Arg494Trp)
NM_004606.5(TAF1):c.204C>G (p.Thr68=)
NM_004606.5(TAF1):c.2122-3T>C
NM_004606.5(TAF1):c.2569+3C>T
NM_004606.5(TAF1):c.2928G>A (p.Gln976=) rs2148371952
NM_004606.5(TAF1):c.4209A>G (p.Thr1403=)
NM_004606.5(TAF1):c.4302C>T (p.Asn1434=)
NM_004606.5(TAF1):c.4812A>G (p.Thr1604=)
NM_004606.5(TAF1):c.4982G>A (p.Arg1661Gln)
NM_004606.5(TAF1):c.5358C>T (p.Asp1786=)
NM_004606.5(TAF1):c.5399+7G>A
NM_004606.5(TAF1):c.627C>G (p.Thr209=)

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.