Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.3056082A>T | CA1434035159 | HTT | n.825-6394A>T n.503+13837A>T c.5+13837A>T (n.5+13837A>T) | dbSNP |
4 | g.3056082A>G | CA11632738 | HTT | n.825-6394A>G n.503+13837A>G c.5+13837A>G (n.5+13837A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |