| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.31810752C>A | CA449805184 | HSPA1L | c.1221G>T (p.Thr407=) c.1413G>T (p.Thr471=) | dbSNP gnomAD v4 |
| 6 | g.31810752C>T | CA3723944 | HSPA1L | c.1221G>A (p.Thr407=) c.1413G>A (p.Thr471=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.31810752C= | CA1619316010 | HSPA1L | c.1221G= (p.Thr407=) c.1413G= (p.Thr471=) | dbSNP |
| 6 | g.31810752C>G | CA449805186 | HSPA1L | c.1221G>C (p.Thr407=) c.1413G>C (p.Thr471=) | dbSNP COSMIC |