Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4860241G>ACA438365840MSX1c.342G>A (p.Pro114=)
dbSNP gnomAD v2 gnomAD v4
4g.4860241G>CCA438365842MSX1c.342G>C (p.Pro114=)
4g.4860241G=CA1435012209MSX1c.342G= (p.Pro114=)
4g.4860241G>TCA438365844MSX1c.342G>T (p.Pro114=)
gnomAD v4
4g.4860242C>ACA356137802MSX1c.343C>A (p.Leu115Ile)
4g.4860242C>GCA356137804MSX1c.343C>G (p.Leu115Val)
4g.4860242C>TCA356137806MSX1c.343C>T (p.Leu115Phe)
4g.4860243T>ACA356137808MSX1c.344T>A (p.Leu115His)
4g.4860243T>CCA356137810MSX1c.344T>C (p.Leu115Pro)
gnomAD v4
4g.4860243T>GCA356137812MSX1c.344T>G (p.Leu115Arg)
4g.4860244C>ACA438365846MSX1c.345C>A (p.Leu115=)
gnomAD v4
4g.4860244C=CA1435012210MSX1c.345C= (p.Leu115=)
4g.4860244C>GCA438365848MSX1c.345C>G (p.Leu115=)
4g.4860244C>TCA438365847MSX1c.345C>T (p.Leu115=)
dbSNP gnomAD v2 gnomAD v4 COSMIC
4g.4860245G>ACA356137814MSX1c.346G>A (p.Gly116Ser)
gnomAD v4
4g.4860245G>CCA356137818MSX1c.346G>C (p.Gly116Arg)
gnomAD v4
4g.4860245G>TCA356137816MSX1c.346G>T (p.Gly116Cys)
gnomAD v4
4g.4860246G>ACA356137819MSX1c.347G>A (p.Gly116Asp)
gnomAD v4
4g.4860246G>CCA356137820MSX1c.347G>C (p.Gly116Ala)
4g.4860246G=CA1435012211MSX1c.347G= (p.Gly116=)
4g.4860246G>TCA356137822MSX1c.347G>T (p.Gly116Val)
dbSNP gnomAD v4
4g.4860247C>ACA438365850MSX1c.348C>A (p.Gly116=)
4g.4860247C=CA1435012212MSX1c.348C= (p.Gly116=)
4g.4860247C>GCA438365851MSX1c.348C>G (p.Gly116=)
dbSNP gnomAD v2 gnomAD v4
4g.4860247C>TCA2832948MSX1c.348C>T (p.Gly116=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4860248C>ACA356137824MSX1c.349C>A (p.His117Asn)
gnomAD v4
4g.4860248C=CA1435012213MSX1c.349C= (p.His117=)
4g.4860248C>GCA356137825MSX1c.349C>G (p.His117Asp)
dbSNP gnomAD v3 gnomAD v4
4g.4860248C>TCA356137826MSX1c.349C>T (p.His117Tyr)
dbSNP gnomAD v4
4g.4860249A=CA1435012214MSX1c.350A= (p.His117=)
4g.4860249A>CCA356137828MSX1c.350A>C (p.His117Pro)
4g.4860249A>GCA356137830MSX1c.350A>G (p.His117Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.4860249A>TCA91668764MSX1c.350A>T (p.His117Leu)
dbSNP
4g.4860250T>ACA356137832MSX1c.351T>A (p.His117Gln)
4g.4860250T>CCA438365855MSX1c.351T>C (p.His117=)
4g.4860250T>GCA356137834MSX1c.351T>G (p.His117Gln)
4g.4860251T>ACA356137839MSX1c.352T>A (p.Phe118Ile)
4g.4860251T>CCA356137836MSX1c.352T>C (p.Phe118Leu)
4g.4860251T>GCA356137838MSX1c.352T>G (p.Phe118Val)
4g.4860252T>ACA356137842MSX1c.353T>A (p.Phe118Tyr)
4g.4860252T>CCA356137843MSX1c.353T>C (p.Phe118Ser)
4g.4860252T>GCA356137845MSX1c.353T>G (p.Phe118Cys)
4g.4860253C>ACA356137846MSX1c.354C>A (p.Phe118Leu)
gnomAD v4
4g.4860253C=CA1435012215MSX1c.354C= (p.Phe118=)
4g.4860253C>GCA356137847MSX1c.354C>G (p.Phe118Leu)
4g.4860253C>TCA438365857MSX1c.354C>T (p.Phe118=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.4860254T>ACA356137849MSX1c.355T>A (p.Ser119Thr)
4g.4860254T>CCA356137850MSX1c.355T>C (p.Ser119Pro)
4g.4860254T>GCA356137852MSX1c.355T>G (p.Ser119Ala)
4g.4860255C>ACA356137854MSX1c.356C>A (p.Ser119Ter)
gnomAD v4

Number of alleles fetched