Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
19g.6718366A>GCA403645273C3n.375T>C
c.191T>C (p.Phe64Ser)
c.314T>C (p.Phe105Ser)
gnomAD v4
19g.6718366A>TCA403645274C3n.375T>A
c.191T>A (p.Phe64Tyr)
c.314T>A (p.Phe105Tyr)
19g.6718367A=CA2320570638C3n.374T=
c.190T= (p.Phe64=)
c.313T= (p.Phe105=)
19g.6718367A>CCA403645276C3n.374T>G
c.190T>G (p.Phe64Val)
c.313T>G (p.Phe105Val)
19g.6718367A>GCA9129846C3n.374T>C
c.190T>C (p.Phe64Leu)
c.313T>C (p.Phe105Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.6718367A>TCA403645277C3n.374T>A
c.190T>A (p.Phe64Ile)
c.313T>A (p.Phe105Ile)
19g.6718368C>ACA403645278C3n.373G>T
c.189G>T (p.Lys63Asn)
c.312G>T (p.Lys104Asn)
19g.6718368C>GCA403645279C3n.373G>C
c.189G>C (p.Lys63Asn)
c.312G>C (p.Lys104Asn)
19g.6718368C>TCA505125206C3n.373G>A
c.189G>A (p.Lys63=)
c.312G>A (p.Lys104=)
19g.6718369T>ACA403645282C3n.372A>T
c.188A>T (p.Lys63Met)
c.311A>T (p.Lys104Met)
19g.6718369T>CCA403645280C3n.372A>G
c.188A>G (p.Lys63Arg)
c.311A>G (p.Lys104Arg)
19g.6718369T>GCA403645281C3n.372A>C
c.188A>C (p.Lys63Thr)
c.311A>C (p.Lys104Thr)
19g.6718370T>ACA403645283C3n.371A>T
c.187A>T (p.Lys63Ter)
c.310A>T (p.Lys104Ter)
19g.6718370T>CCA403645284C3n.371A>G
c.187A>G (p.Lys63Glu)
c.310A>G (p.Lys104Glu)
ClinVar dbSNP gnomAD v4
19g.6718370T>GCA403645285C3n.371A>C
c.187A>C (p.Lys63Gln)
c.310A>C (p.Lys104Gln)
19g.6718370T=CA2320570639C3n.371A=
c.187A= (p.Lys63=)
c.310A= (p.Lys104=)

Number of alleles fetched