Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.31636267T>C | CA449797226 | PRRC2A | c.5683T>C (p.Leu1895=) n.617T>C n.21T>C | dbSNP |
6 | g.31636267T>G | CA3716613 | PRRC2A | c.5683T>G (p.Leu1895Val) n.617T>G n.21T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.31636267T>A | CA363367254 | PRRC2A | c.5683T>A (p.Leu1895Ile) n.617T>A n.21T>A | dbSNP |