ClinVar Miner

List of variants in gene ANO10 reported by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln) rs3772165 0.58882
NM_018075.5(ANO10):c.1293+9A>G rs7616708 0.56196
NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly) rs56389778 0.05750
NM_018075.5(ANO10):c.486C>T (p.Leu162=) rs34829628 0.02348
NM_018075.5(ANO10):c.788G>A (p.Arg263His) rs41289586 0.01896
NM_018075.5(ANO10):c.74A>C (p.Gln25Pro) rs112040665 0.01413
NM_018075.5(ANO10):c.627T>C (p.Ala209=) rs61742945 0.01193
NM_018075.5(ANO10):c.1669-8T>G rs115769245 0.00517
NM_018075.5(ANO10):c.1915-5863G>A rs141400669 0.00503
NM_018075.5(ANO10):c.980A>G (p.Tyr327Cys) rs146569520 0.00359
NM_018075.5(ANO10):c.1133G>A (p.Arg378Gln) rs61732728 0.00281
NM_018075.5(ANO10):c.1915-5816C>A rs146629436 0.00245
NM_018075.5(ANO10):c.1954A>G (p.Met652Val) rs147989825 0.00180
NM_018075.5(ANO10):c.963C>T (p.Phe321=) rs149196477 0.00097
NM_018075.5(ANO10):c.88G>C (p.Glu30Gln) rs147605535 0.00085
NM_018075.5(ANO10):c.1914+3G>A rs113187031 0.00068
NM_018075.5(ANO10):c.566G>A (p.Arg189Gln) rs148873732 0.00056
NM_018075.5(ANO10):c.850C>A (p.Pro284Thr) rs192531429 0.00030
NM_018075.5(ANO10):c.343_345del (p.Asn115del) rs771064874 0.00021
NM_018075.5(ANO10):c.1864A>G (p.Met622Val) rs141806947 0.00019
NM_018075.5(ANO10):c.790G>A (p.Gly264Ser) rs375470443 0.00019
NM_018075.5(ANO10):c.236T>G (p.Met79Arg) rs201275096 0.00017
NM_018075.5(ANO10):c.837A>T (p.Arg279Ser) rs374795191 0.00014
NM_018075.5(ANO10):c.397G>A (p.Glu133Lys) rs571983239 0.00008
NM_018075.5(ANO10):c.512T>C (p.Phe171Ser) rs373386030 0.00004
NM_018075.5(ANO10):c.5A>T (p.Lys2Ile) rs569513041 0.00004
NM_018075.5(ANO10):c.938G>A (p.Arg313His) rs747769148 0.00004
NM_018075.5(ANO10):c.1401G>T (p.Val467=) rs149580265 0.00003
NM_018075.5(ANO10):c.1559C>T (p.Ala520Val) rs150026260 0.00003
NM_018075.5(ANO10):c.1962C>T (p.Ser654=) rs756170502 0.00003
NM_018075.5(ANO10):c.989T>G (p.Leu330Arg) rs1024962328 0.00003
NM_018075.5(ANO10):c.224C>T (p.Ser75Phe) rs769095178 0.00002
NM_018075.5(ANO10):c.1716G>A (p.Ala572=) rs746207433 0.00001
NM_018075.5(ANO10):c.1797+1G>A rs1206950481 0.00001
NM_018075.5(ANO10):c.2T>C (p.Met1Thr) rs531656357 0.00001
NM_018075.5(ANO10):c.305A>G (p.Tyr102Cys) rs754580837 0.00001
NM_018075.5(ANO10):c.312C>G (p.Thr104=) rs757830418 0.00001
NM_018075.5(ANO10):c.338-2A>G rs761765455 0.00001
NM_018075.5(ANO10):c.416A>T (p.Asp139Val) rs1341078381 0.00001
NM_018075.5(ANO10):c.473-2A>T rs1553724533 0.00001
NM_018075.5(ANO10):c.866A>G (p.His289Arg) rs371063079 0.00001
NM_018075.5(ANO10):c.*10G>A
NM_018075.5(ANO10):c.1050C>A (p.Ser350Arg) rs143141504
NM_018075.5(ANO10):c.1056dup (p.Glu353Ter)
NM_018075.5(ANO10):c.1137T>C (p.Tyr379=)
NM_018075.5(ANO10):c.1179_1180del (p.Glu393fs)
NM_018075.5(ANO10):c.1260C>T (p.Ala420=) rs1365986557
NM_018075.5(ANO10):c.1315A>G (p.Thr439Ala) rs1559701894
NM_018075.5(ANO10):c.132dup (p.Asp45fs) rs540331226
NM_018075.5(ANO10):c.1429A>G (p.Thr477Ala)
NM_018075.5(ANO10):c.1585G>T (p.Glu529Ter)
NM_018075.5(ANO10):c.158_169dup (p.Arg53_Leu56dup) rs761124350
NM_018075.5(ANO10):c.159A>G (p.Arg53=) rs533186096
NM_018075.5(ANO10):c.1688G>A (p.Ser563Asn) rs1553709113
NM_018075.5(ANO10):c.1715C>A (p.Ala572Glu) rs759026322
NM_018075.5(ANO10):c.1715C>T (p.Ala572Val) rs759026322
NM_018075.5(ANO10):c.1724G>A (p.Gly575Glu) rs865842244
NM_018075.5(ANO10):c.1753C>A (p.Pro585Thr)
NM_018075.5(ANO10):c.1760C>G (p.Ser587Ter)
NM_018075.5(ANO10):c.1853G>A (p.Arg618Gln)
NM_018075.5(ANO10):c.1866G>A (p.Met622Ile)
NM_018075.5(ANO10):c.1915-5883G>C
NM_018075.5(ANO10):c.341A>G (p.Asn114Ser)
NM_018075.5(ANO10):c.412A>G (p.Lys138Glu)
NM_018075.5(ANO10):c.45C>T (p.Phe15=)
NM_018075.5(ANO10):c.473-2A>G rs1553724533
NM_018075.5(ANO10):c.488C>T (p.Thr163Met)
NM_018075.5(ANO10):c.532G>A (p.Ala178Thr)
NM_018075.5(ANO10):c.602G>A (p.Arg201His)
NM_018075.5(ANO10):c.608A>G (p.Tyr203Cys) rs779190429
NM_018075.5(ANO10):c.712G>C (p.Glu238Gln)
NM_018075.5(ANO10):c.86A>G (p.Glu29Gly)
NM_018075.5(ANO10):c.946C>T (p.Leu316=)
NM_018075.5(ANO10):c.966G>A (p.Val322=)
NM_018075.5(ANO10):c.96del (p.Glu33fs) rs758937084

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.