Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.6718351G>ACA403645241C3n.390C>T
c.206C>T (p.Ala69Val)
c.329C>T (p.Ala110Val)
19g.6718351G>CCA403645243C3n.390C>G
c.206C>G (p.Ala69Gly)
c.329C>G (p.Ala110Gly)
19g.6718351G>TCA403645242C3n.390C>A
c.206C>A (p.Ala69Asp)
c.329C>A (p.Ala110Asp)
19g.6718352C>ACA403645244C3n.389G>T
c.205G>T (p.Ala69Ser)
c.328G>T (p.Ala110Ser)
19g.6718352C>GCA403645245C3n.389G>C
c.205G>C (p.Ala69Pro)
c.328G>C (p.Ala110Pro)
19g.6718352C>TCA403645246C3n.389G>A
c.205G>A (p.Ala69Thr)
c.328G>A (p.Ala110Thr)
19g.6718353C>ACA403645247C3n.388G>T
c.204G>T (p.Gln68His)
c.327G>T (p.Gln109His)
gnomAD v4
19g.6718353C=CA2320570635C3n.388G=
c.204G= (p.Gln68=)
c.327G= (p.Gln109=)
19g.6718353C>GCA304803632C3n.388G>C
c.204G>C (p.Gln68His)
c.327G>C (p.Gln109His)
dbSNP gnomAD v3 gnomAD v4
19g.6718353C>TCA505125197C3n.388G>A
c.204G>A (p.Gln68=)
c.327G>A (p.Gln109=)
19g.6718354T>ACA403645250C3n.387A>T
c.203A>T (p.Gln68Leu)
c.326A>T (p.Gln109Leu)
19g.6718354T>CCA403645249C3n.387A>G
c.203A>G (p.Gln68Arg)
c.326A>G (p.Gln109Arg)
19g.6718354T>GCA403645248C3n.387A>C
c.203A>C (p.Gln68Pro)
c.326A>C (p.Gln109Pro)
19g.6718355G>ACA403645251C3n.386C>T
c.202C>T (p.Gln68Ter)
c.325C>T (p.Gln109Ter)
19g.6718355G>CCA403645252C3n.386C>G
c.202C>G (p.Gln68Glu)
c.325C>G (p.Gln109Glu)
19g.6718355G>TCA403645253C3n.386C>A
c.202C>A (p.Gln68Lys)
c.325C>A (p.Gln109Lys)
19g.6718356C>ACA505125198C3n.385G>T
c.201G>T (p.Val67=)
c.324G>T (p.Val108=)
19g.6718356C>GCA505125199C3n.385G>C
c.201G>C (p.Val67=)
c.324G>C (p.Val108=)
19g.6718356C>TCA505125200C3n.385G>A
c.201G>A (p.Val67=)
c.324G>A (p.Val108=)
gnomAD v4
19g.6718357A>CCA403645254C3n.384T>G
c.200T>G (p.Val67Gly)
c.323T>G (p.Val108Gly)
19g.6718357A>GCA403645255C3n.384T>C
c.200T>C (p.Val67Ala)
c.323T>C (p.Val108Ala)
19g.6718357A>TCA403645256C3n.384T>A
c.200T>A (p.Val67Glu)
c.323T>A (p.Val108Glu)
19g.6718358C>ACA403645257C3n.383G>T
c.199G>T (p.Val67Leu)
c.322G>T (p.Val108Leu)
19g.6718358C=CA2320570636C3n.383G=
c.199G= (p.Val67=)
c.322G= (p.Val108=)
19g.6718358C>GCA403645258C3n.383G>C
c.199G>C (p.Val67Leu)
c.322G>C (p.Val108Leu)
gnomAD v4
19g.6718358C>TCA9129844C3n.383G>A
c.199G>A (p.Val67Met)
c.322G>A (p.Val108Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.6718359G>ACA304803648C3n.382C>T
c.198C>T (p.Thr66=)
c.321C>T (p.Thr107=)
dbSNP gnomAD v3 gnomAD v4
19g.6718359G>CCA9129845C3n.382C>G
c.198C>G (p.Thr66=)
c.321C>G (p.Thr107=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.6718359G=CA2320570637C3n.382C=
c.198C= (p.Thr66=)
c.321C= (p.Thr107=)
19g.6718359G>TCA505125201C3n.382C>A
c.198C>A (p.Thr66=)
c.321C>A (p.Thr107=)
COSMIC
19g.6718360G>ACA403645259C3n.381C>T
c.197C>T (p.Thr66Ile)
c.320C>T (p.Thr107Ile)
19g.6718360G>CCA403645260C3n.381C>G
c.197C>G (p.Thr66Ser)
c.320C>G (p.Thr107Ser)
19g.6718360G>TCA403645261C3n.381C>A
c.197C>A (p.Thr66Asn)
c.320C>A (p.Thr107Asn)
19g.6718361T>ACA403645262C3n.380A>T
c.196A>T (p.Thr66Ser)
c.319A>T (p.Thr107Ser)
gnomAD v4
19g.6718361T>CCA403645263C3n.380A>G
c.196A>G (p.Thr66Ala)
c.319A>G (p.Thr107Ala)
19g.6718361T>GCA403645264C3n.380A>C
c.196A>C (p.Thr66Pro)
c.319A>C (p.Thr107Pro)
19g.6718362C>ACA505125202C3n.379G>T
c.195G>T (p.Val65=)
c.318G>T (p.Val106=)
19g.6718362C>GCA505125204C3n.379G>C
c.195G>C (p.Val65=)
c.318G>C (p.Val106=)
ClinVar gnomAD v4
19g.6718362C>TCA505125203C3n.379G>A
c.195G>A (p.Val65=)
c.318G>A (p.Val106=)
19g.6718362dupCA2587880778C3n.379dup
c.195dup (p.Thr66AspfsTer?)
c.318dup (p.Thr107AspfsTer?)
gnomAD v4
19g.6718363A>CCA403645265C3n.378T>G
c.194T>G (p.Val65Gly)
c.317T>G (p.Val106Gly)
19g.6718363A>GCA403645266C3n.378T>C
c.194T>C (p.Val65Ala)
c.317T>C (p.Val106Ala)
19g.6718363A>TCA403645267C3n.378T>A
c.194T>A (p.Val65Glu)
c.317T>A (p.Val106Glu)
19g.6718364C>ACA403645269C3n.377G>T
c.193G>T (p.Val65Leu)
c.316G>T (p.Val106Leu)
19g.6718364C>GCA403645270C3n.377G>C
c.193G>C (p.Val65Leu)
c.316G>C (p.Val106Leu)
gnomAD v4
19g.6718364C>TCA403645268C3n.377G>A
c.193G>A (p.Val65Met)
c.316G>A (p.Val106Met)
19g.6718365G>ACA505125205C3n.376C>T
c.192C>T (p.Phe64=)
c.315C>T (p.Phe105=)
19g.6718365G>CCA403645272C3n.376C>G
c.192C>G (p.Phe64Leu)
c.315C>G (p.Phe105Leu)
ClinVar
19g.6718365G>TCA403645271C3n.376C>A
c.192C>A (p.Phe64Leu)
c.315C>A (p.Phe105Leu)
19g.6718366A>CCA403645275C3n.375T>G
c.191T>G (p.Phe64Cys)
c.314T>G (p.Phe105Cys)

Number of alleles fetched