| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.149771108G>A | CA11984661 | PPARGC1B | c.78+40688G>A (n.78+40688G>A) n.432+9496G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.149771108G= | CA1590644786 | PPARGC1B | c.78+40688G= (n.78+40688G=) n.432+9496G= | dbSNP |