Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.146340275C>ACA3491216POU4F3c.848C>A (p.Ala283Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.146340275C>TCA236239POU4F3c.848C>T (p.Ala283Val)
 ClinVar dbSNP
5g.146340275C=CA1589086862POU4F3c.848C= (p.Ala283=)
 dbSNP

Number of alleles fetched