Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.16948752G>A | CA8414016 | TNFRSF13B | c.431C>T (p.Ser144Leu) n.434C>T n.335C>T c.293C>T (p.Ser98Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948752G>C | CA8414017 | TNFRSF13B | c.431C>G (p.Ser144Ter) n.434C>G n.335C>G c.293C>G (p.Ser98Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.16948752G>T | CA117397 | TNFRSF13B | c.431C>A (p.Ser144Ter) n.434C>A n.335C>A c.293C>A (p.Ser98Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |