Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.4860264G>T | CA2832952 | MSX1 | c.365G>T (p.Gly122Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.4860264G>A | CA124431 | MSX1 | c.365G>A (p.Gly122Glu) | ClinVar dbSNP gnomAD v4 |
4 | g.4860264G= | CA1435012222 | MSX1 | c.365G= (p.Gly122=) | dbSNP |
4 | g.4860264G>C | CA356137888 | MSX1 | c.365G>C (p.Gly122Ala) | dbSNP gnomAD v4 |