Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.106496119C>TCA481650272POLR3Bc.2778C>T (p.Asp926=)
c.2604C>T (p.Asp868=)
 dbSNP gnomAD v4
12g.106496119C>GCA342789POLR3Bc.2778C>G (p.Asp926Glu)
c.2604C>G (p.Asp868Glu)
 ClinVar dbSNP

Number of alleles fetched