Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.219060168G>T | CA119975 | IHH | c.300C>A (p.Asp100Glu) | ClinVar dbSNP |
2 | g.219060168G>A | CA431419769 | IHH | c.300C>T (p.Asp100=) | dbSNP gnomAD v4 |
2 | g.219060168G= | CA1329042573 | IHH | c.300C= (p.Asp100=) | dbSNP |