Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.186679065C>T | CA1299703 | PTGS2 | c.306G>A (p.Val102=) n.439G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.186679065C>G | CA1299702 | PTGS2 | c.306G>C (p.Val102=) n.439G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.186679065C>A | CA422373364 | PTGS2 | c.306G>T (p.Val102=) n.439G>T | dbSNP gnomAD v4 |
1 | g.186679065C= | CA1139772955 | PTGS2 | c.306G= (p.Val102=) n.439G= | dbSNP |