Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.3856149C>ACA372805526GLIS3c.2333G>T (p.Ser778Ile)
n.775G>T
c.1868G>T (p.Ser623Ile)
n.689G>T
n.873G>T
c.1667G>T (p.Ser556Ile)
9g.3856149C>GCA372805527GLIS3c.2333G>C (p.Ser778Thr)
n.775G>C
c.1868G>C (p.Ser623Thr)
n.689G>C
n.873G>C
c.1667G>C (p.Ser556Thr)
9g.3856149C>TCA372805528GLIS3c.2333G>A (p.Ser778Asn)
n.775G>A
c.1868G>A (p.Ser623Asn)
n.689G>A
n.873G>A
c.1667G>A (p.Ser556Asn)
9g.3856150T>ACA372805529GLIS3c.2332A>T (p.Ser778Cys)
n.774A>T
c.1867A>T (p.Ser623Cys)
n.688A>T
n.872A>T
c.1666A>T (p.Ser556Cys)
9g.3856150T>CCA372805530GLIS3c.2332A>G (p.Ser778Gly)
n.774A>G
c.1867A>G (p.Ser623Gly)
n.688A>G
n.872A>G
c.1666A>G (p.Ser556Gly)
9g.3856150T>GCA372805531GLIS3c.2332A>C (p.Ser778Arg)
n.774A>C
c.1867A>C (p.Ser623Arg)
n.688A>C
n.872A>C
c.1666A>C (p.Ser556Arg)
9g.3856151G>ACA4967827GLIS3c.2331C>T (p.Ile777=)
n.773C>T
c.1866C>T (p.Ile622=)
n.687C>T
n.871C>T
c.1665C>T (p.Ile555=)
dbSNP ExAC gnomAD
9g.3856151G>CCA372805532GLIS3c.2331C>G (p.Ile777Met)
n.773C>G
c.1866C>G (p.Ile622Met)
n.687C>G
n.871C>G
c.1665C>G (p.Ile555Met)
9g.3856151G=CA1828933263GLIS3c.2331C= (p.Ile777=)
n.773C=
c.1866C= (p.Ile622=)
n.687C=
n.871C=
c.1665C= (p.Ile555=)
9g.3856151G>TCA463714809GLIS3c.2331C>A (p.Ile777=)
n.773C>A
c.1866C>A (p.Ile622=)
n.687C>A
n.871C>A
c.1665C>A (p.Ile555=)
9g.3856152A=CA1828933264GLIS3c.2330T= (p.Ile777=)
n.772T=
c.1865T= (p.Ile622=)
n.686T=
n.870T=
c.1664T= (p.Ile555=)
9g.3856152A>CCA372805533GLIS3c.2330T>G (p.Ile777Ser)
n.772T>G
c.1865T>G (p.Ile622Ser)
n.686T>G
n.870T>G
c.1664T>G (p.Ile555Ser)
9g.3856152A>GCA372805534GLIS3c.2330T>C (p.Ile777Thr)
n.772T>C
c.1865T>C (p.Ile622Thr)
n.686T>C
n.870T>C
c.1664T>C (p.Ile555Thr)
9g.3856152A>TCA4967828GLIS3c.2330T>A (p.Ile777Asn)
n.772T>A
c.1865T>A (p.Ile622Asn)
n.686T>A
n.870T>A
c.1664T>A (p.Ile555Asn)
dbSNP ExAC gnomAD
9g.3856153T>ACA372805535GLIS3c.2329A>T (p.Ile777Phe)
n.771A>T
c.1864A>T (p.Ile622Phe)
n.685A>T
n.869A>T
c.1663A>T (p.Ile555Phe)
9g.3856153T>CCA372805537GLIS3c.2329A>G (p.Ile777Val)
n.771A>G
c.1864A>G (p.Ile622Val)
n.685A>G
n.869A>G
c.1663A>G (p.Ile555Val)
9g.3856153T>GCA372805536GLIS3c.2329A>C (p.Ile777Leu)
n.771A>C
c.1864A>C (p.Ile622Leu)
n.685A>C
n.869A>C
c.1663A>C (p.Ile555Leu)
9g.3856153T=CA1828933266GLIS3c.2329A= (p.Ile777=)
n.771A=
c.1864A= (p.Ile622=)
n.685A=
n.869A=
c.1663A= (p.Ile555=)
9g.3856153_3856156delinsTGTGCA1828933265GLIS3c.2326_2329delinsCACA (p.His776=)
n.768_771delinsCACA
c.1861_1864delinsCACA (p.His621=)
n.682_685delinsCACA
n.866_869delinsCACA
c.1660_1663delinsCACA (p.His554=)
9g.3856154G>ACA463714810GLIS3c.2328C>T (p.His776=)
n.770C>T
c.1863C>T (p.His621=)
n.684C>T
n.868C>T
c.1662C>T (p.His554=)
9g.3856154G>CCA188287319GLIS3c.2328C>G (p.His776Gln)
n.770C>G
c.1863C>G (p.His621Gln)
n.684C>G
n.868C>G
c.1662C>G (p.His554Gln)
dbSNP gnomAD
9g.3856154G=CA1828933268GLIS3c.2328C= (p.His776=)
n.770C=
c.1863C= (p.His621=)
n.684C=
n.868C=
c.1662C= (p.His554=)
9g.3856154G>TCA372805538GLIS3c.2328C>A (p.His776Gln)
n.770C>A
c.1863C>A (p.His621Gln)
n.684C>A
n.868C>A
c.1662C>A (p.His554Gln)
9g.3856157_3856159delCA1828933267GLIS3c.2326_2328del (p.His776del)
n.768_770del
c.1861_1863del (p.His621del)
n.682_684del
n.866_868del
c.1660_1662del (p.His554del)
dbSNP
9g.3856155T>ACA372805539GLIS3c.2327A>T (p.His776Leu)
n.769A>T
c.1862A>T (p.His621Leu)
n.683A>T
n.867A>T
c.1661A>T (p.His554Leu)
9g.3856155T>CCA4967829GLIS3c.2327A>G (p.His776Arg)
n.769A>G
c.1862A>G (p.His621Arg)
n.683A>G
n.867A>G
c.1661A>G (p.His554Arg)
dbSNP ExAC gnomAD
9g.3856155T>GCA372805540GLIS3c.2327A>C (p.His776Pro)
n.769A>C
c.1862A>C (p.His621Pro)
n.683A>C
n.867A>C
c.1661A>C (p.His554Pro)
9g.3856155T=CA1828933269GLIS3c.2327A= (p.His776=)
n.769A=
c.1862A= (p.His621=)
n.683A=
n.867A=
c.1661A= (p.His554=)
9g.3856156G>ACA372805541GLIS3c.2326C>T (p.His776Tyr)
n.768C>T
c.1861C>T (p.His621Tyr)
n.682C>T
n.866C>T
c.1660C>T (p.His554Tyr)
9g.3856156G>CCA372805542GLIS3c.2326C>G (p.His776Asp)
n.768C>G
c.1861C>G (p.His621Asp)
n.682C>G
n.866C>G
c.1660C>G (p.His554Asp)
9g.3856156G=CA1828933270GLIS3c.2326C= (p.His776=)
n.768C=
c.1861C= (p.His621=)
n.682C=
n.866C=
c.1660C= (p.His554=)
9g.3856156G>TCA372805543GLIS3c.2326C>A (p.His776Asn)
n.768C>A
c.1861C>A (p.His621Asn)
n.682C>A
n.866C>A
c.1660C>A (p.His554Asn)
9g.3856157G>ACA463714811GLIS3c.2325C>T (p.His775=)
n.767C>T
c.1860C>T (p.His620=)
n.681C>T
n.865C>T
c.1659C>T (p.His553=)
9g.3856157G>CCA372805544GLIS3c.2325C>G (p.His775Gln)
n.767C>G
c.1860C>G (p.His620Gln)
n.681C>G
n.865C>G
c.1659C>G (p.His553Gln)
9g.3856157G=CA1828933271GLIS3c.2325C= (p.His775=)
n.767C=
c.1860C= (p.His620=)
n.681C=
n.865C=
c.1659C= (p.His553=)
9g.3856157G>TCA4967830GLIS3c.2325C>A (p.His775Gln)
n.767C>A
c.1860C>A (p.His620Gln)
n.681C>A
n.865C>A
c.1659C>A (p.His553Gln)
dbSNP ExAC gnomAD
9g.3856158T>ACA372805545GLIS3c.2324A>T (p.His775Leu)
n.766A>T
c.1859A>T (p.His620Leu)
n.680A>T
n.864A>T
c.1658A>T (p.His553Leu)
9g.3856158T>CCA372805546GLIS3c.2324A>G (p.His775Arg)
n.766A>G
c.1859A>G (p.His620Arg)
n.680A>G
n.864A>G
c.1658A>G (p.His553Arg)
9g.3856158T>GCA372805547GLIS3c.2324A>C (p.His775Pro)
n.766A>C
c.1859A>C (p.His620Pro)
n.680A>C
n.864A>C
c.1658A>C (p.His553Pro)
9g.3856159G>ACA4967831GLIS3c.2323C>T (p.His775Tyr)
n.765C>T
c.1858C>T (p.His620Tyr)
n.679C>T
n.863C>T
c.1657C>T (p.His553Tyr)
ClinVar dbSNP ExAC gnomAD
9g.3856159G>CCA372805548GLIS3c.2323C>G (p.His775Asp)
n.765C>G
c.1858C>G (p.His620Asp)
n.679C>G
n.863C>G
c.1657C>G (p.His553Asp)
9g.3856159G=CA1828933272GLIS3c.2323C= (p.His775=)
n.765C=
c.1858C= (p.His620=)
n.679C=
n.863C=
c.1657C= (p.His553=)
9g.3856159G>TCA372805549GLIS3c.2323C>A (p.His775Asn)
n.765C>A
c.1858C>A (p.His620Asn)
n.679C>A
n.863C>A
c.1657C>A (p.His553Asn)
9g.3856160A>CCA463714812GLIS3c.2322T>G (p.Pro774=)
n.764T>G
c.1857T>G (p.Pro619=)
n.678T>G
n.862T>G
c.1656T>G (p.Pro552=)
9g.3856160A>GCA463714814GLIS3c.2322T>C (p.Pro774=)
n.764T>C
c.1857T>C (p.Pro619=)
n.678T>C
n.862T>C
c.1656T>C (p.Pro552=)
9g.3856160A>TCA463714813GLIS3c.2322T>A (p.Pro774=)
n.764T>A
c.1857T>A (p.Pro619=)
n.678T>A
n.862T>A
c.1656T>A (p.Pro552=)
9g.3856161G>ACA372805550GLIS3c.2321C>T (p.Pro774Leu)
n.763C>T
c.1856C>T (p.Pro619Leu)
n.677C>T
n.861C>T
c.1655C>T (p.Pro552Leu)
COSMIC COSMIC
9g.3856161G>CCA372805551GLIS3c.2321C>G (p.Pro774Arg)
n.763C>G
c.1856C>G (p.Pro619Arg)
n.677C>G
n.861C>G
c.1655C>G (p.Pro552Arg)
9g.3856161G>TCA372805552GLIS3c.2321C>A (p.Pro774His)
n.763C>A
c.1856C>A (p.Pro619His)
n.677C>A
n.861C>A
c.1655C>A (p.Pro552His)
9g.3856162G>ACA372805553GLIS3c.2320C>T (p.Pro774Ser)
n.762C>T
c.1855C>T (p.Pro619Ser)
n.676C>T
n.860C>T
c.1654C>T (p.Pro552Ser)

Number of alleles fetched