Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.43687681T>C | CA10048020 | RRP1B | c.1307T>C (p.Leu436Pro) n.970T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.43687681T>A | CA410401270 | RRP1B | c.1307T>A (p.Leu436Gln) n.970T>A | dbSNP gnomAD v4 |
21 | g.43687681T= | CA2391301975 | RRP1B | c.1307T= (p.Leu436=) n.970T= | dbSNP |
21 | g.43687681T>G | CA410401271 | RRP1B | c.1307T>G (p.Leu436Arg) n.970T>G | dbSNP gnomAD v4 |