Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4860264G>TCA2832952MSX1c.365G>T (p.Gly122Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.4860264G>ACA124431MSX1c.365G>A (p.Gly122Glu)
ClinVar dbSNP gnomAD v4
4g.4860264G=CA1435012222MSX1c.365G= (p.Gly122=)
dbSNP
4g.4860264G>CCA356137888MSX1c.365G>C (p.Gly122Ala)
dbSNP gnomAD v4

Number of alleles fetched