Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.135055071T>C | CA452338975 | HBS1L | c.89-4424A>G (n.89-4424A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.135055071T>A | CA452338976 | HBS1L | c.89-4424A>T (n.89-4424A>T) | dbSNP |
6 | g.135055071T>G | CA249794 | HBS1L | c.89-4424A>C (n.89-4424A>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.135055071T= | CA1665740040 | HBS1L | c.89-4424A= (n.89-4424A=) | dbSNP |