Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.119872005G>T | CA414190327 | NDUFA1 | c.94G>T (p.Gly32Trp) | dbSNP gnomAD v2 gnomAD v4 |
X | g.119872005G>C | CA090926 | NDUFA1 | c.94G>C (p.Gly32Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.119872005G>A | CA10503532 | NDUFA1 | c.94G>A (p.Gly32Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |