Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.6665009T>G | CA403621962 | TNFSF14 | c.640A>C (p.Lys214Gln) c.532A>C (p.Lys178Gln) c.332+2104A>C (n.332+2104A>C) n.812+2104A>C c.298+2104A>C (n.298+2104A>C) n.824+2104A>C | dbSNP |
19 | g.6665009T>A | CA403621954 | TNFSF14 | c.640A>T (p.Lys214Ter) c.532A>T (p.Lys178Ter) c.332+2104A>T (n.332+2104A>T) n.812+2104A>T c.298+2104A>T (n.298+2104A>T) n.824+2104A>T | dbSNP |
19 | g.6665009T>C | CA9127964 | TNFSF14 | c.640A>G (p.Lys214Glu) c.532A>G (p.Lys178Glu) c.332+2104A>G (n.332+2104A>G) n.812+2104A>G c.298+2104A>G (n.298+2104A>G) n.824+2104A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |