ClinVar Miner

List of variants in gene STAT1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_007315.4(STAT1):c.*855G>A rs188557905 0.00037
NM_007315.4(STAT1):c.*121C>T rs938403650 0.00022
NM_007315.4(STAT1):c.*461del rs201656062 0.00018
NM_007315.4(STAT1):c.*670T>G rs186033487 0.00018
NM_007315.4(STAT1):c.*281C>T rs762197567 0.00006
NM_007315.4(STAT1):c.*137T>C rs571207686 0.00005
NM_007315.4(STAT1):c.*362T>C rs886055377 0.00003
NM_007315.4(STAT1):c.*921G>C rs886055376 0.00003
NM_007315.4(STAT1):c.1713T>G (p.Pro571=) rs772114461 0.00003
NM_007315.4(STAT1):c.201A>G (p.Gln67=) rs148148052 0.00003
NM_007315.4(STAT1):c.2087C>A (p.Pro696His) rs138723664 0.00003
NM_007315.3(STAT1):c.*1628A>G rs886055373 0.00002
NM_007315.4(STAT1):c.*1066C>T rs780655672 0.00002
NM_007315.4(STAT1):c.*959G>A rs967454724 0.00002
NM_007315.4(STAT1):c.372+13C>T rs911316159 0.00002
NM_007315.4(STAT1):c.735C>T (p.Ser245=) rs768384746 0.00002
NM_007315.4(STAT1):c.*1012A>G rs1691307752 0.00001
NM_007315.4(STAT1):c.*1163T>C rs1329457174 0.00001
NM_007315.4(STAT1):c.*1260A>G rs886055374 0.00001
NM_007315.4(STAT1):c.*1514A>G rs1433022831 0.00001
NM_007315.4(STAT1):c.-293C>G rs886055382 0.00001
NM_007315.4(STAT1):c.1222-3T>C rs886055379 0.00001
NM_007315.4(STAT1):c.1683C>T (p.Ile561=) rs886055378 0.00001
NM_007315.4(STAT1):c.18A>C (p.Glu6Asp) rs986212030 0.00001
NM_007315.4(STAT1):c.*1094G>C rs550489659
NM_007315.4(STAT1):c.*1154C>T rs977912956
NM_007315.4(STAT1):c.*1175A>T rs967975098
NM_007315.4(STAT1):c.*1187C>G rs1691294583
NM_007315.4(STAT1):c.*1298A>G rs1691288268
NM_007315.4(STAT1):c.*1317G>A rs368576923
NM_007315.4(STAT1):c.*1473C>T rs755752702
NM_007315.4(STAT1):c.*1482A>G rs1691271835
NM_007315.4(STAT1):c.*363A>G rs1691358240
NM_007315.4(STAT1):c.*461G>A rs200344731
NM_007315.4(STAT1):c.*645T>G rs1285562768
NM_007315.4(STAT1):c.*932A>C rs886055375
NM_007315.4(STAT1):c.1248C>T (p.Gly416=) rs140787216
NM_007315.4(STAT1):c.1256C>G (p.Thr419Arg) rs1347113886
NM_007315.4(STAT1):c.1967C>T (p.Ala656Val) rs1574638429
NM_007315.4(STAT1):c.501A>G (p.Gln167=) rs1167103580
NM_007315.4(STAT1):c.714G>A (p.Glu238=) rs886055380
NM_007315.4(STAT1):c.786-12G>C rs562518878

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.