Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.4860357C>T | CA356138154 | MSX1 | c.458C>T (p.Pro153Leu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.4860357C>G | CA2832979 | MSX1 | c.458C>G (p.Pro153Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.4860357C>A | CA124432 | MSX1 | c.458C>A (p.Pro153Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |