| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.32222629A>G | CA3740279 | NOTCH4 | c.333T>C (p.Gly111=) n.462T>C n.472T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.32222629A>C | CA449728780 | NOTCH4 | c.333T>G (p.Gly111=) n.462T>G n.472T>G | dbSNP gnomAD v4 |
| 6 | g.32222629A>T | CA449728782 | NOTCH4 | c.333T>A (p.Gly111=) n.462T>A n.472T>A | dbSNP |