Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.101473652A>CCA476546355TRPC6c.1866T>G (p.Pro622=)
c.1518T>G (p.Pro506=)
c.1701T>G (p.Pro567=)
c.1632T>G (p.Pro544=)
n.2222T>G
11g.101473652A>GCA476546356TRPC6c.1866T>C (p.Pro622=)
c.1518T>C (p.Pro506=)
c.1701T>C (p.Pro567=)
c.1632T>C (p.Pro544=)
n.2222T>C
11g.101473652A>TCA476546357TRPC6c.1866T>A (p.Pro622=)
c.1518T>A (p.Pro506=)
c.1701T>A (p.Pro567=)
c.1632T>A (p.Pro544=)
n.2222T>A
11g.101473653G>ACA382440279TRPC6c.1865C>T (p.Pro622Leu)
c.1517C>T (p.Pro506Leu)
c.1700C>T (p.Pro567Leu)
c.1631C>T (p.Pro544Leu)
n.2221C>T
11g.101473653G>CCA382440280TRPC6c.1865C>G (p.Pro622Arg)
c.1517C>G (p.Pro506Arg)
c.1700C>G (p.Pro567Arg)
c.1631C>G (p.Pro544Arg)
n.2221C>G
 dbSNP gnomAD v3 gnomAD v4
11g.101473653G=CA1995831445TRPC6c.1865C= (p.Pro622=)
c.1517C= (p.Pro506=)
c.1700C= (p.Pro567=)
c.1631C= (p.Pro544=)
n.2221C=
11g.101473653G>TCA382440281TRPC6c.1865C>A (p.Pro622His)
c.1517C>A (p.Pro506His)
c.1700C>A (p.Pro567His)
c.1631C>A (p.Pro544His)
n.2221C>A
11g.101473654G>ACA382440282TRPC6c.1864C>T (p.Pro622Ser)
c.1516C>T (p.Pro506Ser)
c.1699C>T (p.Pro567Ser)
c.1630C>T (p.Pro544Ser)
n.2220C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.101473654G>CCA382440284TRPC6c.1864C>G (p.Pro622Ala)
c.1516C>G (p.Pro506Ala)
c.1699C>G (p.Pro567Ala)
c.1630C>G (p.Pro544Ala)
n.2220C>G
11g.101473654G=CA1995831448TRPC6c.1864C= (p.Pro622=)
c.1516C= (p.Pro506=)
c.1699C= (p.Pro567=)
c.1630C= (p.Pro544=)
n.2220C=
11g.101473654G>TCA382440283TRPC6c.1864C>A (p.Pro622Thr)
c.1516C>A (p.Pro506Thr)
c.1699C>A (p.Pro567Thr)
c.1630C>A (p.Pro544Thr)
n.2220C>A
11g.101473655T>ACA476546361TRPC6c.1863A>T (p.Gly621=)
c.1515A>T (p.Gly505=)
c.1698A>T (p.Gly566=)
c.1629A>T (p.Gly543=)
n.2219A>T
11g.101473655T>CCA476546363TRPC6c.1863A>G (p.Gly621=)
c.1515A>G (p.Gly505=)
c.1698A>G (p.Gly566=)
c.1629A>G (p.Gly543=)
n.2219A>G
11g.101473655T>GCA476546362TRPC6c.1863A>C (p.Gly621=)
c.1515A>C (p.Gly505=)
c.1698A>C (p.Gly566=)
c.1629A>C (p.Gly543=)
n.2219A>C
11g.101473656C>ACA382440285TRPC6c.1862G>T (p.Gly621Val)
c.1514G>T (p.Gly505Val)
c.1697G>T (p.Gly566Val)
c.1628G>T (p.Gly543Val)
n.2218G>T
11g.101473656C>GCA382440286TRPC6c.1862G>C (p.Gly621Ala)
c.1514G>C (p.Gly505Ala)
c.1697G>C (p.Gly566Ala)
c.1628G>C (p.Gly543Ala)
n.2218G>C
11g.101473656C>TCA382440287TRPC6c.1862G>A (p.Gly621Glu)
c.1514G>A (p.Gly505Glu)
c.1697G>A (p.Gly566Glu)
c.1628G>A (p.Gly543Glu)
n.2218G>A
11g.101473657C>ACA382440288TRPC6c.1861G>T (p.Gly621Ter)
c.1513G>T (p.Gly505Ter)
c.1696G>T (p.Gly566Ter)
c.1627G>T (p.Gly543Ter)
n.2217G>T
11g.101473657C>GCA382440289TRPC6c.1861G>C (p.Gly621Arg)
c.1513G>C (p.Gly505Arg)
c.1696G>C (p.Gly566Arg)
c.1627G>C (p.Gly543Arg)
n.2217G>C
11g.101473657C>TCA382440290TRPC6c.1861G>A (p.Gly621Arg)
c.1513G>A (p.Gly505Arg)
c.1696G>A (p.Gly566Arg)
c.1627G>A (p.Gly543Arg)
n.2217G>A
11g.101473658A>CCA382440291TRPC6c.1860T>G (p.Phe620Leu)
c.1512T>G (p.Phe504Leu)
c.1695T>G (p.Phe565Leu)
c.1626T>G (p.Phe542Leu)
n.2216T>G
11g.101473658A>GCA476546366TRPC6c.1860T>C (p.Phe620=)
c.1512T>C (p.Phe504=)
c.1695T>C (p.Phe565=)
c.1626T>C (p.Phe542=)
n.2216T>C
11g.101473658A>TCA382440292TRPC6c.1860T>A (p.Phe620Leu)
c.1512T>A (p.Phe504Leu)
c.1695T>A (p.Phe565Leu)
c.1626T>A (p.Phe542Leu)
n.2216T>A
11g.101473659A>CCA382440293TRPC6c.1859T>G (p.Phe620Cys)
c.1511T>G (p.Phe504Cys)
c.1694T>G (p.Phe565Cys)
c.1625T>G (p.Phe542Cys)
n.2215T>G
11g.101473659A>GCA382440294TRPC6c.1859T>C (p.Phe620Ser)
c.1511T>C (p.Phe504Ser)
c.1694T>C (p.Phe565Ser)
c.1625T>C (p.Phe542Ser)
n.2215T>C
11g.101473659A>TCA382440295TRPC6c.1859T>A (p.Phe620Tyr)
c.1511T>A (p.Phe504Tyr)
c.1694T>A (p.Phe565Tyr)
c.1625T>A (p.Phe542Tyr)
n.2215T>A
11g.101473660A>CCA382440296TRPC6c.1858T>G (p.Phe620Val)
c.1510T>G (p.Phe504Val)
c.1693T>G (p.Phe565Val)
c.1624T>G (p.Phe542Val)
n.2214T>G
11g.101473660A>GCA382440298TRPC6c.1858T>C (p.Phe620Leu)
c.1510T>C (p.Phe504Leu)
c.1693T>C (p.Phe565Leu)
c.1624T>C (p.Phe542Leu)
n.2214T>C
11g.101473660A>TCA382440297TRPC6c.1858T>A (p.Phe620Ile)
c.1510T>A (p.Phe504Ile)
c.1693T>A (p.Phe565Ile)
c.1624T>A (p.Phe542Ile)
n.2214T>A
11g.101473661G>ACA476546369TRPC6c.1857C>T (p.Ser619=)
c.1509C>T (p.Ser503=)
c.1692C>T (p.Ser564=)
c.1623C>T (p.Ser541=)
n.2213C>T
11g.101473661G>CCA382440299TRPC6c.1857C>G (p.Ser619Arg)
c.1509C>G (p.Ser503Arg)
c.1692C>G (p.Ser564Arg)
c.1623C>G (p.Ser541Arg)
n.2213C>G
11g.101473661G>TCA382440300TRPC6c.1857C>A (p.Ser619Arg)
c.1509C>A (p.Ser503Arg)
c.1692C>A (p.Ser564Arg)
c.1623C>A (p.Ser541Arg)
n.2213C>A
11g.101473662C>ACA382440301TRPC6c.1856G>T (p.Ser619Ile)
c.1508G>T (p.Ser503Ile)
c.1691G>T (p.Ser564Ile)
c.1622G>T (p.Ser541Ile)
n.2212G>T
11g.101473662C>GCA382440302TRPC6c.1856G>C (p.Ser619Thr)
c.1508G>C (p.Ser503Thr)
c.1691G>C (p.Ser564Thr)
c.1622G>C (p.Ser541Thr)
n.2212G>C
11g.101473662C>TCA382440303TRPC6c.1856G>A (p.Ser619Asn)
c.1508G>A (p.Ser503Asn)
c.1691G>A (p.Ser564Asn)
c.1622G>A (p.Ser541Asn)
n.2212G>A
11g.101473663T>ACA382440304TRPC6c.1855A>T (p.Ser619Cys)
c.1507A>T (p.Ser503Cys)
c.1690A>T (p.Ser564Cys)
c.1621A>T (p.Ser541Cys)
n.2211A>T
11g.101473663T>CCA382440305TRPC6c.1855A>G (p.Ser619Gly)
c.1507A>G (p.Ser503Gly)
c.1690A>G (p.Ser564Gly)
c.1621A>G (p.Ser541Gly)
n.2211A>G
11g.101473663T>GCA382440306TRPC6c.1855A>C (p.Ser619Arg)
c.1507A>C (p.Ser503Arg)
c.1690A>C (p.Ser564Arg)
c.1621A>C (p.Ser541Arg)
n.2211A>C
11g.101473664T>ACA382440307TRPC6c.1854A>T (p.Glu618Asp)
c.1506A>T (p.Glu502Asp)
c.1689A>T (p.Glu563Asp)
c.1620A>T (p.Glu540Asp)
n.2210A>T
11g.101473664T>CCA476546373TRPC6c.1854A>G (p.Glu618=)
c.1506A>G (p.Glu502=)
c.1689A>G (p.Glu563=)
c.1620A>G (p.Glu540=)
n.2210A>G
11g.101473664T>GCA382440308TRPC6c.1854A>C (p.Glu618Asp)
c.1506A>C (p.Glu502Asp)
c.1689A>C (p.Glu563Asp)
c.1620A>C (p.Glu540Asp)
n.2210A>C
11g.101473665T>ACA382440309TRPC6c.1853A>T (p.Glu618Val)
c.1505A>T (p.Glu502Val)
c.1688A>T (p.Glu563Val)
c.1619A>T (p.Glu540Val)
n.2209A>T
11g.101473665T>CCA382440310TRPC6c.1853A>G (p.Glu618Gly)
c.1505A>G (p.Glu502Gly)
c.1688A>G (p.Glu563Gly)
c.1619A>G (p.Glu540Gly)
n.2209A>G
11g.101473665T>GCA382440311TRPC6c.1853A>C (p.Glu618Ala)
c.1505A>C (p.Glu502Ala)
c.1688A>C (p.Glu563Ala)
c.1619A>C (p.Glu540Ala)
n.2209A>C
11g.101473666C>ACA382440314TRPC6c.1852G>T (p.Glu618Ter)
c.1504G>T (p.Glu502Ter)
c.1687G>T (p.Glu563Ter)
c.1618G>T (p.Glu540Ter)
n.2208G>T
11g.101473666C>GCA382440313TRPC6c.1852G>C (p.Glu618Gln)
c.1504G>C (p.Glu502Gln)
c.1687G>C (p.Glu563Gln)
c.1618G>C (p.Glu540Gln)
n.2208G>C
11g.101473666C>TCA382440312TRPC6c.1852G>A (p.Glu618Lys)
c.1504G>A (p.Glu502Lys)
c.1687G>A (p.Glu563Lys)
c.1618G>A (p.Glu540Lys)
n.2208G>A
11g.101473667A>CCA382440315TRPC6c.1851T>G (p.Asn617Lys)
c.1503T>G (p.Asn501Lys)
c.1686T>G (p.Asn562Lys)
c.1617T>G (p.Asn539Lys)
n.2207T>G
11g.101473667A>GCA476546382TRPC6c.1851T>C (p.Asn617=)
c.1503T>C (p.Asn501=)
c.1686T>C (p.Asn562=)
c.1617T>C (p.Asn539=)
n.2207T>C
11g.101473667A>TCA382440316TRPC6c.1851T>A (p.Asn617Lys)
c.1503T>A (p.Asn501Lys)
c.1686T>A (p.Asn562Lys)
c.1617T>A (p.Asn539Lys)
n.2207T>A

Number of alleles fetched