Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.109097622A>T | CA1809870539 | TRHR | c.789+9321A>T (n.789+9321A>T) | dbSNP |
8 | g.109097622A>G | CA845420192 | TRHR | c.789+9321A>G (n.789+9321A>G) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.109097622A>C | CA12772089 | TRHR | c.789+9321A>C (n.789+9321A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |