Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.36575624G>A | CA5950247 | RAG1,RAG2 | c.2320G>A (p.Glu774Lys) n.479C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575624G>T | CA122877 | RAG1,RAG2 | c.2320G>T (p.Glu774Ter) n.479C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.36575624G= | CA1964167682 | RAG1,RAG2 | c.2320G= (p.Glu774=) n.479C= | dbSNP |