Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.53906876T>GCA344603PRKCGc.2075T>G (p.Val692Gly)
n.1476T>G
c.1967T>G (p.Val656Gly)
c.1166T>G (p.Val389Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.53906876T>CCA9640768PRKCGc.2075T>C (p.Val692Ala)
n.1476T>C
c.1967T>C (p.Val656Ala)
c.1166T>C (p.Val389Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.53906876T>ACA407420670PRKCGc.2075T>A (p.Val692Glu)
n.1476T>A
c.1967T>A (p.Val656Glu)
c.1166T>A (p.Val389Glu)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched