Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.16948752G>ACA8414016TNFRSF13Bc.431C>T (p.Ser144Leu)
n.434C>T
n.335C>T
c.293C>T (p.Ser98Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.16948752G>CCA8414017TNFRSF13Bc.431C>G (p.Ser144Ter)
n.434C>G
n.335C>G
c.293C>G (p.Ser98Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.16948752G>TCA117397TNFRSF13Bc.431C>A (p.Ser144Ter)
n.434C>A
n.335C>A
c.293C>A (p.Ser98Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched