Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49457977T>CCA364404669MMUTc.467A>G (p.Asp156Gly)
dbSNP gnomAD v3 gnomAD v4
6g.49457977T>ACA3847103MMUTc.467A>T (p.Asp156Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.49457977T=CA1627395396MMUTc.467A= (p.Asp156=)
dbSNP

Number of alleles fetched