| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.136207828A>T | CA121568 | FHL1 | c.416A>T (p.His139Leu) c.368A>T (p.His123Leu) c.455A>T (p.His152Leu) n.72A>T n.418A>T n.779A>T | ClinVar dbSNP |
| X | g.136207828A>G | CA414608363 | FHL1 | c.416A>G (p.His139Arg) c.368A>G (p.His123Arg) c.455A>G (p.His152Arg) n.72A>G n.418A>G n.779A>G | ClinVar dbSNP |