Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.165021265C>TCA115006SIc.3218G>A (p.Gly1073Asp)
c.3119G>A (p.Gly1040Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.165021265C>ACA355040909SIc.3218G>T (p.Gly1073Val)
c.3119G>T (p.Gly1040Val)
 dbSNP gnomAD v4

Number of alleles fetched