| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.48965326C>T | CA10575529 | FTL | c.-182C>T (n.-182C>T) c.329C>T (p.Ala110Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.48965326C= | CA2340161151 | FTL | c.-182C= (n.-182C=) c.329C= (p.Ala110=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.48965326C>T | CA10575529 | FTL | c.-182C>T (n.-182C>T) c.329C>T (p.Ala110Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.48965326C= | CA2340161151 | FTL | c.-182C= (n.-182C=) c.329C= (p.Ala110=) | dbSNP |