Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.36575322_36575995delinsGCG | CA2740093700 | RAG1 | c.2018_2691delinsGCG (p.Ala673GlyfsTer7) | ClinVar |
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 |
11 | g.36575653A>C | CA474032444 | RAG1,RAG2 | c.2349A>C (p.Ser783=) n.450T>G | |
11 | g.36575653A>G | CA474032445 | RAG1,RAG2 | c.2349A>G (p.Ser783=) n.450T>C | |
11 | g.36575653A>T | CA474032446 | RAG1,RAG2 | c.2349A>T (p.Ser783=) n.450T>A | |
11 | g.36575654G>A | CA380154523 | RAG1,RAG2 | c.2350G>A (p.Ala784Thr) n.449C>T | |
11 | g.36575654G>C | CA380154524 | RAG1,RAG2 | c.2350G>C (p.Ala784Pro) n.449C>G | |
11 | g.36575654G>T | CA380154522 | RAG1,RAG2 | c.2350G>T (p.Ala784Ser) n.449C>A | gnomAD v4 |
11 | g.36575655C>A | CA380154525 | RAG1,RAG2 | c.2351C>A (p.Ala784Asp) n.448G>T | |
11 | g.36575655C>G | CA380154527 | RAG1,RAG2 | c.2351C>G (p.Ala784Gly) n.448G>C | |
11 | g.36575655C>T | CA380154526 | RAG1,RAG2 | c.2351C>T (p.Ala784Val) n.448G>A | gnomAD v4 |
11 | g.36575656T>A | CA474032447 | RAG1,RAG2 | c.2352T>A (p.Ala784=) n.447A>T | |
11 | g.36575656T>C | CA474032448 | RAG1,RAG2 | c.2352T>C (p.Ala784=) n.447A>G | |
11 | g.36575656T>G | CA474032449 | RAG1,RAG2 | c.2352T>G (p.Ala784=) n.447A>C | |
11 | g.36575657A>C | CA380154528 | RAG1,RAG2 | c.2353A>C (p.Lys785Gln) n.446T>G | |
11 | g.36575657A>G | CA380154530 | RAG1,RAG2 | c.2353A>G (p.Lys785Glu) n.446T>C | |
11 | g.36575657A>T | CA380154529 | RAG1,RAG2 | c.2353A>T (p.Lys785Ter) n.446T>A | |
11 | g.36575658A>C | CA380154531 | RAG1,RAG2 | c.2354A>C (p.Lys785Thr) n.445T>G | |
11 | g.36575658A>G | CA380154532 | RAG1,RAG2 | c.2354A>G (p.Lys785Arg) n.445T>C | |
11 | g.36575658A>T | CA380154533 | RAG1,RAG2 | c.2354A>T (p.Lys785Ile) n.445T>A | |
11 | g.36575659A>C | CA380154534 | RAG1,RAG2 | c.2355A>C (p.Lys785Asn) n.444T>G | |
11 | g.36575659A>G | CA474032450 | RAG1,RAG2 | c.2355A>G (p.Lys785=) n.444T>C | gnomAD v4 |
11 | g.36575659A>T | CA380154535 | RAG1,RAG2 | c.2355A>T (p.Lys785Asn) n.444T>A | |
11 | g.36575660C>A | CA380154536 | RAG1,RAG2 | c.2356C>A (p.Pro786Thr) n.443G>T | |
11 | g.36575660C= | CA1964167768 | RAG1,RAG2 | c.2356C= (p.Pro786=) n.443G= | |
11 | g.36575660C>G | CA380154537 | RAG1,RAG2 | c.2356C>G (p.Pro786Ala) n.443G>C | |
11 | g.36575660C>T | CA380154538 | RAG1,RAG2 | c.2356C>T (p.Pro786Ser) n.443G>A | dbSNP |
11 | g.36575661C>A | CA380154539 | RAG1,RAG2 | c.2357C>A (p.Pro786His) n.442G>T | |
11 | g.36575661C= | CA1964167771 | RAG1,RAG2 | c.2357C= (p.Pro786=) n.442G= | |
11 | g.36575661C>G | CA380154540 | RAG1,RAG2 | c.2357C>G (p.Pro786Arg) n.442G>C | |
11 | g.36575661C>T | CA380154541 | RAG1,RAG2 | c.2357C>T (p.Pro786Leu) n.442G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.36575662T>A | CA474032451 | RAG1,RAG2 | c.2358T>A (p.Pro786=) n.441A>T | |
11 | g.36575662T>C | CA474032452 | RAG1,RAG2 | c.2358T>C (p.Pro786=) n.441A>G | |
11 | g.36575662T>G | CA474032453 | RAG1,RAG2 | c.2358T>G (p.Pro786=) n.441A>C | |
11 | g.36575663T>A | CA380154542 | RAG1,RAG2 | c.2359T>A (p.Phe787Ile) n.440A>T | |
11 | g.36575663T>C | CA380154544 | RAG1,RAG2 | c.2359T>C (p.Phe787Leu) n.440A>G | gnomAD v4 |
11 | g.36575663T>G | CA380154543 | RAG1,RAG2 | c.2359T>G (p.Phe787Val) n.440A>C | |
11 | g.36575664T>A | CA380154545 | RAG1,RAG2 | c.2360T>A (p.Phe787Tyr) n.439A>T | |
11 | g.36575664T>C | CA380154546 | RAG1,RAG2 | c.2360T>C (p.Phe787Ser) n.439A>G | |
11 | g.36575664T>G | CA380154547 | RAG1,RAG2 | c.2360T>G (p.Phe787Cys) n.439A>C | |
11 | g.36575665C>A | CA380154548 | RAG1,RAG2 | c.2361C>A (p.Phe787Leu) n.438G>T | |
11 | g.36575665C= | CA1964167775 | RAG1,RAG2 | c.2361C= (p.Phe787=) n.438G= | |
11 | g.36575665C>G | CA380154549 | RAG1,RAG2 | c.2361C>G (p.Phe787Leu) n.438G>C | |
11 | g.36575665C>T | CA5950252 | RAG1,RAG2 | c.2361C>T (p.Phe787=) n.438G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |