Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.36575322_36575995delinsGCG | CA2740093700 | RAG1 | c.2018_2691delinsGCG (p.Ala673GlyfsTer7) | ClinVar |
11 | g.36575638G>A | CA474032434 | RAG1,RAG2 | c.2334G>A (p.Arg778=) n.465C>T | |
11 | g.36575638G>C | CA474032432 | RAG1,RAG2 | c.2334G>C (p.Arg778=) n.465C>G | |
11 | g.36575638G>T | CA474032433 | RAG1,RAG2 | c.2334G>T (p.Arg778=) n.465C>A | |
11 | g.36575639G>A | CA380154494 | RAG1,RAG2 | c.2335G>A (p.Val779Met) n.464C>T | |
11 | g.36575639G>C | CA380154493 | RAG1,RAG2 | c.2335G>C (p.Val779Leu) n.464C>G | |
11 | g.36575639G>T | CA380154492 | RAG1,RAG2 | c.2335G>T (p.Val779Leu) n.464C>A | |
11 | g.36575640T>A | CA380154495 | RAG1,RAG2 | c.2336T>A (p.Val779Glu) n.463A>T | |
11 | g.36575640T>C | CA380154496 | RAG1,RAG2 | c.2336T>C (p.Val779Ala) n.463A>G | gnomAD v4 |
11 | g.36575640T>G | CA380154497 | RAG1,RAG2 | c.2336T>G (p.Val779Gly) n.463A>C | |
11 | g.36575641G>A | CA474032435 | RAG1,RAG2 | c.2337G>A (p.Val779=) n.462C>T | dbSNP gnomAD v2 |
11 | g.36575641G>C | CA474032436 | RAG1,RAG2 | c.2337G>C (p.Val779=) n.462C>G | |
11 | g.36575641G= | CA1964167748 | RAG1,RAG2 | c.2337G= (p.Val779=) n.462C= | |
11 | g.36575641G>T | CA474032437 | RAG1,RAG2 | c.2337G>T (p.Val779=) n.462C>A | |
11 | g.36575642A>C | CA380154498 | RAG1,RAG2 | c.2338A>C (p.Lys780Gln) n.461T>G | |
11 | g.36575642A>G | CA380154499 | RAG1,RAG2 | c.2338A>G (p.Lys780Glu) n.461T>C | |
11 | g.36575642A>T | CA380154500 | RAG1,RAG2 | c.2338A>T (p.Lys780Ter) n.461T>A | |
11 | g.36575643A>C | CA380154503 | RAG1,RAG2 | c.2339A>C (p.Lys780Thr) n.460T>G | |
11 | g.36575643A>G | CA380154501 | RAG1,RAG2 | c.2339A>G (p.Lys780Arg) n.460T>C | |
11 | g.36575643A>T | CA380154502 | RAG1,RAG2 | c.2339A>T (p.Lys780Ile) n.460T>A | |
11 | g.36575644A>C | CA380154504 | RAG1,RAG2 | c.2340A>C (p.Lys780Asn) n.459T>G | |
11 | g.36575644A>G | CA474032438 | RAG1,RAG2 | c.2340A>G (p.Lys780=) n.459T>C | |
11 | g.36575644A>T | CA380154505 | RAG1,RAG2 | c.2340A>T (p.Lys780Asn) n.459T>A | COSMIC |
11 | g.36575645G>A | CA380154506 | RAG1,RAG2 | c.2341G>A (p.Gly781Arg) n.458C>T | |
11 | g.36575645G>C | CA380154507 | RAG1,RAG2 | c.2341G>C (p.Gly781Arg) n.458C>G | gnomAD v4 |
11 | g.36575645G>T | CA380154508 | RAG1,RAG2 | c.2341G>T (p.Gly781Trp) n.458C>A | gnomAD v4 |
11 | g.36575646G>A | CA380154509 | RAG1,RAG2 | c.2342G>A (p.Gly781Glu) n.457C>T | gnomAD v4 |
11 | g.36575646G>C | CA380154511 | RAG1,RAG2 | c.2342G>C (p.Gly781Ala) n.457C>G | |
11 | g.36575646G>T | CA380154510 | RAG1,RAG2 | c.2342G>T (p.Gly781Val) n.457C>A | |
11 | g.36575647G>A | CA474032439 | RAG1,RAG2 | c.2343G>A (p.Gly781=) n.456C>T | ClinVar dbSNP |
11 | g.36575647G>C | CA474032440 | RAG1,RAG2 | c.2343G>C (p.Gly781=) n.456C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575647G= | CA1964167749 | RAG1,RAG2 | c.2343G= (p.Gly781=) n.456C= | |
11 | g.36575647G>T | CA220601514 | RAG1,RAG2 | c.2343G>T (p.Gly781=) n.456C>A | ClinVar dbSNP gnomAD v4 |
11 | g.36575648G>A | CA380154512 | RAG1,RAG2 | c.2344G>A (p.Val782Ile) n.455C>T | dbSNP |
11 | g.36575648G>C | CA380154513 | RAG1,RAG2 | c.2344G>C (p.Val782Leu) n.455C>G | |
11 | g.36575648G>T | CA380154514 | RAG1,RAG2 | c.2344G>T (p.Val782Phe) n.455C>A | gnomAD v4 |
11 | g.36575649T>A | CA220601518 | RAG1,RAG2 | c.2345T>A (p.Val782Asp) n.454A>T | ClinVar dbSNP gnomAD v4 |
11 | g.36575649T>C | CA380154515 | RAG1,RAG2 | c.2345T>C (p.Val782Ala) n.454A>G | |
11 | g.36575649T>G | CA380154516 | RAG1,RAG2 | c.2345T>G (p.Val782Gly) n.454A>C | |
11 | g.36575649T= | CA1964167753 | RAG1,RAG2 | c.2345T= (p.Val782=) n.454A= | |
11 | g.36575650C>A | CA474032441 | RAG1,RAG2 | c.2346C>A (p.Val782=) n.453G>T | |
11 | g.36575650C>G | CA474032442 | RAG1,RAG2 | c.2346C>G (p.Val782=) n.453G>C | |
11 | g.36575650C>T | CA474032443 | RAG1,RAG2 | c.2346C>T (p.Val782=) n.453G>A | |
11 | g.36575651T>A | CA380154517 | RAG1,RAG2 | c.2347T>A (p.Ser783Thr) n.452A>T | |
11 | g.36575651T>C | CA380154518 | RAG1,RAG2 | c.2347T>C (p.Ser783Pro) n.452A>G | |
11 | g.36575651T>G | CA380154519 | RAG1,RAG2 | c.2347T>G (p.Ser783Ala) n.452A>C | |
11 | g.36575652C>A | CA380154520 | RAG1,RAG2 | c.2348C>A (p.Ser783Ter) n.451G>T | |
11 | g.36575652C= | CA1964167759 | RAG1,RAG2 | c.2348C= (p.Ser783=) n.451G= | |
11 | g.36575652C>G | CA5950251 | RAG1,RAG2 | c.2348C>G (p.Ser783Ter) n.451G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575652C>T | CA380154521 | RAG1,RAG2 | c.2348C>T (p.Ser783Leu) n.451G>A | dbSNP |