ClinVar Miner

List of variants in gene ANO10 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018075.5(ANO10):c.88G>C (p.Glu30Gln) rs147605535 0.00085
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.1559C>T (p.Ala520Val) rs150026260 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.305A>G (p.Tyr102Cys) rs754580837 0.00001
NM_018075.5(ANO10):c.416A>T (p.Asp139Val) rs1341078381 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.1137T>C (p.Tyr379=)
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.1429A>G (p.Thr477Ala)
NM_018075.5(ANO10):c.158_169dup (p.Arg53_Leu56dup) rs761124350
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.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.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=)

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.