| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.74082499C>T | CA470171148 | VCL | c.829C>T (p.Leu277=) n.332-18555C>T n.3632C>T c.*584C>T (n.*584C>T) c.832C>T (p.Leu278=) n.90-4772G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.74082499C>A | CA121941 | VCL | c.829C>A (p.Leu277Met) n.332-18555C>A n.3632C>A c.*584C>A (n.*584C>A) c.832C>A (p.Leu278Met) n.90-4772G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.74082499C= | CA1919897697 | VCL | c.829C= (p.Leu277=) n.332-18555C= n.3632C= c.*584C= (n.*584C=) c.832C= (p.Leu278=) n.90-4772G= | dbSNP |