Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.10046292A>T | CA42427122 | KLF11 | c.185A>T (p.Gln62Leu) c.134A>T (p.Gln45Leu) | dbSNP |
2 | g.10046292A>G | CA153422 | KLF11 | c.185A>G (p.Gln62Arg) c.134A>G (p.Gln45Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.10046292A= | CA2488330335 | KLF11 | c.185A= (p.Gln62=) c.134A= (p.Gln45=) | dbSNP |