Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.17816872C>ACA404760580INSL3c.378G>T (p.Leu126=)
c.473G>T (p.Ter158Leu)
c.399G>T
19g.17816872C>GCA404760581INSL3c.378G>C (p.Leu126=)
c.473G>C (p.Ter158Ser)
c.399G>C
19g.17816872C>TCA506002133INSL3c.378G>A (p.Leu126=)
c.473G>A (p.Ter158=)
c.399G>A
19g.17816873A>CCA404760582INSL3c.377T>G (p.Leu126Arg)
c.472T>G (p.Ter158Gly)
c.398T>G
19g.17816873A>GCA404760583INSL3c.377T>C (p.Leu126Pro)
c.472T>C (p.Ter158Arg)
c.398T>C
19g.17816873A>TCA404760584INSL3c.377T>A (p.Leu126Gln)
c.472T>A (p.Ter158Arg)
c.398T>A
19g.17816874G>ACA506002134INSL3c.376C>T (p.Leu126=)
c.471C>T (p.Cys157=)
c.397C>T
19g.17816874G>CCA404760585INSL3c.376C>G (p.Leu126Val)
c.471C>G (p.Cys157Trp)
c.397C>G
19g.17816874G>TCA404760586INSL3c.376C>A (p.Leu126Met)
c.471C>A (p.Cys157Ter)
c.397C>A
19g.17816875C>ACA404760587INSL3c.375G>T (p.Leu125=)
c.470G>T (p.Cys157Phe)
c.396G>T
 gnomAD v4
19g.17816875C>GCA404760588INSL3c.375G>C (p.Leu125=)
c.470G>C (p.Cys157Ser)
c.396G>C
19g.17816875C>TCA404760589INSL3c.375G>A (p.Leu125=)
c.470G>A (p.Cys157Tyr)
c.396G>A
19g.17816876A>CCA404760590INSL3c.374T>G (p.Leu125Arg)
c.469T>G (p.Cys157Gly)
c.395T>G
19g.17816876A>GCA404760591INSL3c.374T>C (p.Leu125Pro)
c.469T>C (p.Cys157Arg)
c.395T>C
19g.17816876A>TCA404760592INSL3c.374T>A (p.Leu125Gln)
c.469T>A (p.Cys157Ser)
c.395T>A
19g.17816877G>ACA506002139INSL3c.373C>T (p.Leu125=)
c.468C>T (p.Thr156=)
c.394C>T
19g.17816877G>CCA404760594INSL3c.373C>G (p.Leu125Val)
c.468C>G (p.Thr156=)
c.394C>G
19g.17816877G>TCA404760593INSL3c.373C>A (p.Leu125Met)
c.468C>A (p.Thr156=)
c.394C>A
19g.17816878G>ACA404760595INSL3c.372C>T (p.Asp124=)
c.467C>T (p.Thr156Ile)
c.393C>T
19g.17816878G>CCA9301222INSL3c.372C>G (p.Asp124Glu)
c.467C>G (p.Thr156Ser)
c.393C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.17816878G=CA2326044684INSL3c.372C= (p.Asp124=)
c.467C= (p.Thr156=)
c.393C=
19g.17816878G>TCA9301223INSL3c.372C>A (p.Asp124Glu)
c.467C>A (p.Thr156Asn)
c.393C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.17816879T>ACA404760596INSL3c.371A>T (p.Asp124Val)
c.466A>T (p.Thr156Ser)
c.392A>T
19g.17816879T>CCA404760598INSL3c.371A>G (p.Asp124Gly)
c.466A>G (p.Thr156Ala)
c.392A>G
 gnomAD v4
19g.17816879T>GCA404760597INSL3c.371A>C (p.Asp124Ala)
c.466A>C (p.Thr156Pro)
c.392A>C
19g.17816880C>ACA404760599INSL3c.370G>T (p.Asp124Tyr)
c.465G>T (p.Lys155Asn)
c.391G>T
 COSMIC
19g.17816880C>GCA404760600INSL3c.370G>C (p.Asp124His)
c.465G>C (p.Lys155Asn)
c.391G>C
19g.17816880C>TCA404760601INSL3c.370G>A (p.Asp124Asn)
c.465G>A (p.Lys155=)
c.391G>A
19g.17816881T>ACA404760602INSL3c.369A>T (p.Gln123His)
c.464A>T (p.Lys155Met)
c.390A>T
19g.17816881T>CCA404760603INSL3c.369A>G (p.Gln123=)
c.464A>G (p.Lys155Arg)
c.390A>G
19g.17816881T>GCA404760604INSL3c.369A>C (p.Gln123His)
c.464A>C (p.Lys155Thr)
c.390A>C
19g.17816882T>ACA404760605INSL3c.368A>T (p.Gln123Leu)
c.463A>T (p.Lys155Ter)
c.389A>T
19g.17816882T>CCA404760606INSL3c.368A>G (p.Gln123Arg)
c.463A>G (p.Lys155Glu)
c.389A>G
19g.17816882T>GCA404760607INSL3c.368A>C (p.Gln123Pro)
c.463A>C (p.Lys155Gln)
c.389A>C
19g.17816883G>ACA404760608INSL3c.367C>T (p.Gln123Ter)
c.462C>T (p.Asn154=)
c.388C>T
 gnomAD v4
19g.17816883G>CCA404760609INSL3c.367C>G (p.Gln123Glu)
c.462C>G (p.Asn154Lys)
c.388C>G
19g.17816883G>TCA404760610INSL3c.367C>A (p.Gln123Lys)
c.462C>A (p.Asn154Lys)
c.388C>A
19g.17816884T>ACA404760611INSL3c.366A>T (p.Gln122His)
c.461A>T (p.Asn154Ile)
c.387A>T
19g.17816884T>CCA306110477INSL3c.366A>G (p.Gln122=)
c.461A>G (p.Asn154Ser)
c.387A>G
 dbSNP gnomAD v2 gnomAD v4
19g.17816884T>GCA404760612INSL3c.366A>C (p.Gln122His)
c.461A>C (p.Asn154Thr)
c.387A>C
19g.17816884T=CA2326044685INSL3c.366A= (p.Gln122=)
c.461A= (p.Asn154=)
c.387A=
19g.17816885T>ACA404760613INSL3c.365A>T (p.Gln122Leu)
c.460A>T (p.Asn154Tyr)
c.386A>T
19g.17816885T>CCA404760614INSL3c.365A>G (p.Gln122Arg)
c.460A>G (p.Asn154Asp)
c.386A>G
19g.17816885T>GCA404760615INSL3c.365A>C (p.Gln122Pro)
c.460A>C (p.Asn154His)
c.386A>C
19g.17816886G>ACA9301224INSL3c.364C>T (p.Gln122Ter)
c.459C>T (p.Pro153=)
c.385C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.17816886G>CCA404760616INSL3c.364C>G (p.Gln122Glu)
c.459C>G (p.Pro153=)
c.385C>G
 dbSNP gnomAD v2 gnomAD v4
19g.17816886G=CA2326044686INSL3c.364C= (p.Gln122=)
c.459C= (p.Pro153=)
c.385C=
19g.17816886G>TCA404760617INSL3c.364C>A (p.Gln122Lys)
c.459C>A (p.Pro153=)
c.385C>A
 COSMIC
19g.17816887G>ACA306110479INSL3c.363C>T (p.Thr121=)
c.458C>T (p.Pro153Leu)
c.384C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.17816887G>CCA404760618INSL3c.363C>G (p.Thr121=)
c.458C>G (p.Pro153Arg)
c.384C>G

Number of alleles fetched