Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.172445659G>C | CA1420510580 | GHSR | c.797-194C>G (n.797-194C>G) | dbSNP |
3 | g.172445659G>A | CA15238458 | GHSR | c.797-194C>T (n.797-194C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.172445659G>T | CA1420510579 | GHSR | c.797-194C>A (n.797-194C>A) | dbSNP |