Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.36575322_36575995delinsGCG | CA2740093700 | RAG1 | c.2018_2691delinsGCG (p.Ala673GlyfsTer7) | ClinVar |
11 | g.36575584T>A | CA380154378 | RAG1,RAG2 | c.2280T>A (p.Tyr760Ter) n.519A>T | |
11 | g.36575584T>C | CA474032402 | RAG1,RAG2 | c.2280T>C (p.Tyr760=) n.519A>G | |
11 | g.36575584T>G | CA380154379 | RAG1,RAG2 | c.2280T>G (p.Tyr760Ter) n.519A>C | |
11 | g.36575585G>A | CA380154380 | RAG1,RAG2 | c.2281G>A (p.Glu761Lys) n.518C>T | |
11 | g.36575585G>C | CA380154382 | RAG1,RAG2 | c.2281G>C (p.Glu761Gln) n.518C>G | |
11 | g.36575585G>T | CA380154381 | RAG1,RAG2 | c.2281G>T (p.Glu761Ter) n.518C>A | |
11 | g.36575586A>C | CA380154383 | RAG1,RAG2 | c.2282A>C (p.Glu761Ala) n.517T>G | |
11 | g.36575586A>G | CA380154384 | RAG1,RAG2 | c.2282A>G (p.Glu761Gly) n.517T>C | |
11 | g.36575586A>T | CA380154385 | RAG1,RAG2 | c.2282A>T (p.Glu761Val) n.517T>A | |
11 | g.36575587G>A | CA474032403 | RAG1,RAG2 | c.2283G>A (p.Glu761=) n.516C>T | |
11 | g.36575587G>C | CA380154386 | RAG1,RAG2 | c.2283G>C (p.Glu761Asp) n.516C>G | |
11 | g.36575587G>T | CA380154387 | RAG1,RAG2 | c.2283G>T (p.Glu761Asp) n.516C>A | |
11 | g.36575588G>A | CA5950241 | RAG1,RAG2 | c.2284G>A (p.Val762Ile) n.515C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575588G>C | CA380154388 | RAG1,RAG2 | c.2284G>C (p.Val762Leu) n.515C>G | |
11 | g.36575588G= | CA1964167611 | RAG1,RAG2 | c.2284G= (p.Val762=) n.515C= | |
11 | g.36575588G>T | CA380154389 | RAG1,RAG2 | c.2284G>T (p.Val762Phe) n.515C>A | |
11 | g.36575589T>A | CA380154390 | RAG1,RAG2 | c.2285T>A (p.Val762Asp) n.514A>T | |
11 | g.36575589T>C | CA380154391 | RAG1,RAG2 | c.2285T>C (p.Val762Ala) n.514A>G | |
11 | g.36575589T>G | CA380154392 | RAG1,RAG2 | c.2285T>G (p.Val762Gly) n.514A>C | |
11 | g.36575590C>A | CA474032404 | RAG1,RAG2 | c.2286C>A (p.Val762=) n.513G>T | |
11 | g.36575590C= | CA1964167614 | RAG1,RAG2 | c.2286C= (p.Val762=) n.513G= | |
11 | g.36575590C>G | CA5950242 | RAG1,RAG2 | c.2286C>G (p.Val762=) n.513G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575590C>T | CA474032405 | RAG1,RAG2 | c.2286C>T (p.Val762=) n.513G>A | dbSNP |
11 | g.36575591T>A | CA380154395 | RAG1,RAG2 | c.2287T>A (p.Trp763Arg) n.512A>T | |
11 | g.36575591T>C | CA380154394 | RAG1,RAG2 | c.2287T>C (p.Trp763Arg) n.512A>G | |
11 | g.36575591T>G | CA380154393 | RAG1,RAG2 | c.2287T>G (p.Trp763Gly) n.512A>C | |
11 | g.36575592G>A | CA380154396 | RAG1,RAG2 | c.2288G>A (p.Trp763Ter) n.511C>T | |
11 | g.36575592G>C | CA380154397 | RAG1,RAG2 | c.2288G>C (p.Trp763Ser) n.511C>G | |
11 | g.36575592G>T | CA380154398 | RAG1,RAG2 | c.2288G>T (p.Trp763Leu) n.511C>A | |
11 | g.36575593G>A | CA380154399 | RAG1,RAG2 | c.2289G>A (p.Trp763Ter) n.510C>T | |
11 | g.36575593G>C | CA380154400 | RAG1,RAG2 | c.2289G>C (p.Trp763Cys) n.510C>G | |
11 | g.36575593G>T | CA380154401 | RAG1,RAG2 | c.2289G>T (p.Trp763Cys) n.510C>A | |
11 | g.36575594C>A | CA380154402 | RAG1,RAG2 | c.2290C>A (p.Arg764Ser) n.509G>T | gnomAD v4 |
11 | g.36575594C= | CA1964167617 | RAG1,RAG2 | c.2290C= (p.Arg764=) n.509G= | |
11 | g.36575594C>G | CA380154403 | RAG1,RAG2 | c.2290C>G (p.Arg764Gly) n.509G>C | gnomAD v4 |
11 | g.36575594C>T | CA380154404 | RAG1,RAG2 | c.2290C>T (p.Arg764Cys) n.509G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.36575595G>A | CA5950243 | RAG1,RAG2 | c.2291G>A (p.Arg764His) n.508C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.36575595G>C | CA380154405 | RAG1,RAG2 | c.2291G>C (p.Arg764Pro) n.508C>G | |
11 | g.36575595G= | CA1964167622 | RAG1,RAG2 | c.2291G= (p.Arg764=) n.508C= | |
11 | g.36575595G>T | CA380154406 | RAG1,RAG2 | c.2291G>T (p.Arg764Leu) n.508C>A | COSMIC |
11 | g.36575596T>A | CA474032406 | RAG1,RAG2 | c.2292T>A (p.Arg764=) n.507A>T | |
11 | g.36575596T>C | CA474032407 | RAG1,RAG2 | c.2292T>C (p.Arg764=) n.507A>G | |
11 | g.36575596T>G | CA474032408 | RAG1,RAG2 | c.2292T>G (p.Arg764=) n.507A>C | |
11 | g.36575597T>A | CA380154409 | RAG1,RAG2 | c.2293T>A (p.Ser765Thr) n.506A>T | ClinVar |
11 | g.36575597T>C | CA380154408 | RAG1,RAG2 | c.2293T>C (p.Ser765Pro) n.506A>G | |
11 | g.36575597T>G | CA380154407 | RAG1,RAG2 | c.2293T>G (p.Ser765Ala) n.506A>C | |
11 | g.36575598C>A | CA380154410 | RAG1,RAG2 | c.2294C>A (p.Ser765Tyr) n.505G>T | |
11 | g.36575598C>G | CA380154412 | RAG1,RAG2 | c.2294C>G (p.Ser765Cys) n.505G>C | |
11 | g.36575598C>T | CA380154411 | RAG1,RAG2 | c.2294C>T (p.Ser765Phe) n.505G>A | |
11 | g.36575599C>A | CA474032409 | RAG1,RAG2 | c.2295C>A (p.Ser765=) n.504G>T | |
11 | g.36575599C>G | CA474032410 | RAG1,RAG2 | c.2295C>G (p.Ser765=) n.504G>C | |
11 | g.36575599C>T | CA474032411 | RAG1,RAG2 | c.2295C>T (p.Ser765=) n.504G>A | |
11 | g.36575600A>C | CA380154413 | RAG1,RAG2 | c.2296A>C (p.Asn766His) n.503T>G | |
11 | g.36575600A>G | CA380154415 | RAG1,RAG2 | c.2296A>G (p.Asn766Asp) n.503T>C | |
11 | g.36575600A>T | CA380154414 | RAG1,RAG2 | c.2296A>T (p.Asn766Tyr) n.503T>A | |
11 | g.36575601A= | CA1964167625 | RAG1,RAG2 | c.2297A= (p.Asn766=) n.502T= | |
11 | g.36575601A>C | CA380154416 | RAG1,RAG2 | c.2297A>C (p.Asn766Thr) n.502T>G | |
11 | g.36575601A>G | CA380154418 | RAG1,RAG2 | c.2297A>G (p.Asn766Ser) n.502T>C | |
11 | g.36575601A>T | CA380154417 | RAG1,RAG2 | c.2297A>T (p.Asn766Ile) n.502T>A | dbSNP gnomAD v4 |
11 | g.36575602C>A | CA380154419 | RAG1,RAG2 | c.2298C>A (p.Asn766Lys) n.501G>T | |
11 | g.36575602C>G | CA380154420 | RAG1,RAG2 | c.2298C>G (p.Asn766Lys) n.501G>C | |
11 | g.36575602C>T | CA474032412 | RAG1,RAG2 | c.2298C>T (p.Asn766=) n.501G>A | |
11 | g.36575603C>A | CA380154421 | RAG1,RAG2 | c.2299C>A (p.Pro767Thr) n.500G>T | gnomAD v4 |
11 | g.36575603C>G | CA380154422 | RAG1,RAG2 | c.2299C>G (p.Pro767Ala) n.500G>C | |
11 | g.36575603C>T | CA380154423 | RAG1,RAG2 | c.2299C>T (p.Pro767Ser) n.500G>A | gnomAD v4 |
11 | g.36575604C>A | CA380154424 | RAG1,RAG2 | c.2300C>A (p.Pro767His) n.499G>T | |
11 | g.36575604C= | CA1964167630 | RAG1,RAG2 | c.2300C= (p.Pro767=) n.499G= | |
11 | g.36575604C>G | CA380154425 | RAG1,RAG2 | c.2300C>G (p.Pro767Arg) n.499G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575604C>T | CA380154426 | RAG1,RAG2 | c.2300C>T (p.Pro767Leu) n.499G>A | gnomAD v4 |
11 | g.36575605T>A | CA474032413 | RAG1,RAG2 | c.2301T>A (p.Pro767=) n.498A>T | |
11 | g.36575605T>C | CA474032414 | RAG1,RAG2 | c.2301T>C (p.Pro767=) n.498A>G | |
11 | g.36575605T>G | CA474032415 | RAG1,RAG2 | c.2301T>G (p.Pro767=) n.498A>C | |
11 | g.36575606T>A | CA380154427 | RAG1,RAG2 | c.2302T>A (p.Tyr768Asn) n.497A>T | |
11 | g.36575606T>C | CA380154428 | RAG1,RAG2 | c.2302T>C (p.Tyr768His) n.497A>G | |
11 | g.36575606T>G | CA380154429 | RAG1,RAG2 | c.2302T>G (p.Tyr768Asp) n.497A>C | |
11 | g.36575607A>C | CA380154432 | RAG1,RAG2 | c.2303A>C (p.Tyr768Ser) n.496T>G | |
11 | g.36575607A>G | CA380154431 | RAG1,RAG2 | c.2303A>G (p.Tyr768Cys) n.496T>C | |
11 | g.36575607A>T | CA380154430 | RAG1,RAG2 | c.2303A>T (p.Tyr768Phe) n.496T>A | |
11 | g.36575608C>A | CA380154433 | RAG1,RAG2 | c.2304C>A (p.Tyr768Ter) n.495G>T | gnomAD v4 |
11 | g.36575608C= | CA1964167633 | RAG1,RAG2 | c.2304C= (p.Tyr768=) n.495G= | |
11 | g.36575608C>G | CA380154434 | RAG1,RAG2 | c.2304C>G (p.Tyr768Ter) n.495G>C | |
11 | g.36575608C>T | CA5950244 | RAG1,RAG2 | c.2304C>T (p.Tyr768=) n.495G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.36575609C>A | CA380154435 | RAG1,RAG2 | c.2305C>A (p.His769Asn) n.494G>T | |
11 | g.36575609C>G | CA380154436 | RAG1,RAG2 | c.2305C>G (p.His769Asp) n.494G>C | |
11 | g.36575609C>T | CA380154437 | RAG1,RAG2 | c.2305C>T (p.His769Tyr) n.494G>A | |
11 | g.36575610A= | CA1964167636 | RAG1,RAG2 | c.2306A= (p.His769=) n.493T= | |
11 | g.36575610A>C | CA380154438 | RAG1,RAG2 | c.2306A>C (p.His769Pro) n.493T>G | |
11 | g.36575610A>G | CA220601462 | RAG1,RAG2 | c.2306A>G (p.His769Arg) n.493T>C | ClinVar dbSNP gnomAD v4 |
11 | g.36575610A>T | CA380154439 | RAG1,RAG2 | c.2306A>T (p.His769Leu) n.493T>A | |
11 | g.36575611T>A | CA380154440 | RAG1,RAG2 | c.2307T>A (p.His769Gln) n.492A>T | |
11 | g.36575611T>C | CA474032416 | RAG1,RAG2 | c.2307T>C (p.His769=) n.492A>G | ClinVar gnomAD v4 |
11 | g.36575611T>G | CA380154441 | RAG1,RAG2 | c.2307T>G (p.His769Gln) n.492A>C | |
11 | g.36575612G>A | CA220601466 | RAG1,RAG2 | c.2308G>A (p.Glu770Lys) n.491C>T | dbSNP COSMIC |
11 | g.36575612G>C | CA380154443 | RAG1,RAG2 | c.2308G>C (p.Glu770Gln) n.491C>G | |
11 | g.36575612G= | CA1964167642 | RAG1,RAG2 | c.2308G= (p.Glu770=) n.491C= | |
11 | g.36575612G>T | CA380154442 | RAG1,RAG2 | c.2308G>T (p.Glu770Ter) n.491C>A | |
11 | g.36575613A>C | CA380154444 | RAG1,RAG2 | c.2309A>C (p.Glu770Ala) n.490T>G | |
11 | g.36575613A>G | CA380154445 | RAG1,RAG2 | c.2309A>G (p.Glu770Gly) n.490T>C | |
11 | g.36575613A>T | CA380154446 | RAG1,RAG2 | c.2309A>T (p.Glu770Val) n.490T>A | |
11 | g.36575614G>A | CA220601470 | RAG1,RAG2 | c.2310G>A (p.Glu770=) n.489C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575614G>C | CA380154447 | RAG1,RAG2 | c.2310G>C (p.Glu770Asp) n.489C>G | ClinVar |
11 | g.36575614G= | CA1964167647 | RAG1,RAG2 | c.2310G= (p.Glu770=) n.489C= | |
11 | g.36575614G>T | CA380154448 | RAG1,RAG2 | c.2310G>T (p.Glu770Asp) n.489C>A | |
11 | g.36575615T>A | CA5950245 | RAG1,RAG2 | c.2311T>A (p.Ser771Thr) n.488A>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575615T>C | CA380154449 | RAG1,RAG2 | c.2311T>C (p.Ser771Pro) n.488A>G | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575615T>G | CA380154450 | RAG1,RAG2 | c.2311T>G (p.Ser771Ala) n.488A>C | |
11 | g.36575615T= | CA1964167654 | RAG1,RAG2 | c.2311T= (p.Ser771=) n.488A= | |
11 | g.36575616C>A | CA380154451 | RAG1,RAG2 | c.2312C>A (p.Ser771Tyr) n.487G>T | gnomAD v4 |
11 | g.36575616C>G | CA380154452 | RAG1,RAG2 | c.2312C>G (p.Ser771Cys) n.487G>C | gnomAD v4 |
11 | g.36575616C>T | CA380154453 | RAG1,RAG2 | c.2312C>T (p.Ser771Phe) n.487G>A | |
11 | g.36575617T>A | CA474032418 | RAG1,RAG2 | c.2313T>A (p.Ser771=) n.486A>T | |
11 | g.36575617T>C | CA220601486 | RAG1,RAG2 | c.2313T>C (p.Ser771=) n.486A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575617T>G | CA474032417 | RAG1,RAG2 | c.2313T>G (p.Ser771=) n.486A>C | |
11 | g.36575617T= | CA1964167657 | RAG1,RAG2 | c.2313T= (p.Ser771=) n.486A= | |
11 | g.36575618G>A | CA380154454 | RAG1,RAG2 | c.2314G>A (p.Val772Met) n.485C>T | gnomAD v4 |
11 | g.36575618G>C | CA380154456 | RAG1,RAG2 | c.2314G>C (p.Val772Leu) n.485C>G | gnomAD v4 |
11 | g.36575618G>T | CA380154455 | RAG1,RAG2 | c.2314G>T (p.Val772Leu) n.485C>A | |
11 | g.36575619T>A | CA380154457 | RAG1,RAG2 | c.2315T>A (p.Val772Glu) n.484A>T | |
11 | g.36575619T>C | CA380154458 | RAG1,RAG2 | c.2315T>C (p.Val772Ala) n.484A>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.36575619T>G | CA380154459 | RAG1,RAG2 | c.2315T>G (p.Val772Gly) n.484A>C | |
11 | g.36575619T= | CA1964167665 | RAG1,RAG2 | c.2315T= (p.Val772=) n.484A= | |
11 | g.36575619_36575620delinsTG | CA1964167670 | RAG1,RAG2 | c.2315_2316delinsTG (p.Val772=) n.483_484delinsCA | |
11 | g.36575620G>A | CA474032419 | RAG1,RAG2 | c.2316G>A (p.Val772=) n.483C>T | |
11 | g.36575620G>C | CA474032420 | RAG1,RAG2 | c.2316G>C (p.Val772=) n.483C>G | |
11 | g.36575620G>T | CA474032421 | RAG1,RAG2 | c.2316G>T (p.Val772=) n.483C>A | |
11 | g.36575621del | CA1964167673 | RAG1,RAG2 | c.2317del (p.Glu773LysfsTer7) n.483del | dbSNP |
11 | g.36575621G>A | CA380154460 | RAG1,RAG2 | c.2317G>A (p.Glu773Lys) n.482C>T | |
11 | g.36575621G>C | CA380154461 | RAG1,RAG2 | c.2317G>C (p.Glu773Gln) n.482C>G | |
11 | g.36575621G>T | CA380154462 | RAG1,RAG2 | c.2317G>T (p.Glu773Ter) n.482C>A | |
11 | g.36575622A= | CA1964167677 | RAG1,RAG2 | c.2318A= (p.Glu773=) n.481T= | |
11 | g.36575622A>C | CA380154463 | RAG1,RAG2 | c.2318A>C (p.Glu773Ala) n.481T>G | |
11 | g.36575622A>G | CA5950246 | RAG1,RAG2 | c.2318A>G (p.Glu773Gly) n.481T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.36575622A>T | CA380154464 | RAG1,RAG2 | c.2318A>T (p.Glu773Val) n.481T>A | |
11 | g.36575623A>C | CA380154465 | RAG1,RAG2 | c.2319A>C (p.Glu773Asp) n.480T>G | |
11 | g.36575623A>G | CA474032422 | RAG1,RAG2 | c.2319A>G (p.Glu773=) n.480T>C | |
11 | g.36575623A>T | CA380154466 | RAG1,RAG2 | c.2319A>T (p.Glu773Asp) n.480T>A | |
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>C | CA380154467 | RAG1,RAG2 | c.2320G>C (p.Glu774Gln) n.479C>G | |
11 | g.36575624G= | CA1964167682 | RAG1,RAG2 | c.2320G= (p.Glu774=) n.479C= | |
11 | g.36575624G>T | CA122877 | RAG1,RAG2 | c.2320G>T (p.Glu774Ter) n.479C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.36575625A>C | CA380154469 | RAG1,RAG2 | c.2321A>C (p.Glu774Ala) n.478T>G | |
11 | g.36575625A>G | CA380154468 | RAG1,RAG2 | c.2321A>G (p.Glu774Gly) n.478T>C | |
11 | g.36575625A>T | CA380154470 | RAG1,RAG2 | c.2321A>T (p.Glu774Val) n.478T>A | |
11 | g.36575626A>C | CA380154471 | RAG1,RAG2 | c.2322A>C (p.Glu774Asp) n.477T>G | |
11 | g.36575626A>G | CA474032423 | RAG1,RAG2 | c.2322A>G (p.Glu774=) n.477T>C | |
11 | g.36575626A>T | CA380154472 | RAG1,RAG2 | c.2322A>T (p.Glu774Asp) n.477T>A | |
11 | g.36575627C>A | CA380154473 | RAG1,RAG2 | c.2323C>A (p.Leu775Met) n.476G>T | |
11 | g.36575627C>G | CA380154474 | RAG1,RAG2 | c.2323C>G (p.Leu775Val) n.476G>C | |
11 | g.36575627C>T | CA474032424 | RAG1,RAG2 | c.2323C>T (p.Leu775=) n.476G>A | |
11 | g.36575628T>A | CA380154475 | RAG1,RAG2 | c.2324T>A (p.Leu775Gln) n.475A>T | |
11 | g.36575628T>C | CA380154476 | RAG1,RAG2 | c.2324T>C (p.Leu775Pro) n.475A>G | |
11 | g.36575628T>G | CA5950248 | RAG1,RAG2 | c.2324T>G (p.Leu775Arg) n.475A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.36575628T= | CA1964167690 | RAG1,RAG2 | c.2324T= (p.Leu775=) n.475A= | |
11 | g.36575629G>A | CA5950249 | RAG1,RAG2 | c.2325G>A (p.Leu775=) n.474C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.36575629G>C | CA474032426 | RAG1,RAG2 | c.2325G>C (p.Leu775=) n.474C>G | |
11 | g.36575629G= | CA1964167694 | RAG1,RAG2 | c.2325G= (p.Leu775=) n.474C= | |
11 | g.36575629G>T | CA474032425 | RAG1,RAG2 | c.2325G>T (p.Leu775=) n.474C>A | |
11 | g.36575630C>A | CA474032427 | RAG1,RAG2 | c.2326C>A (p.Arg776=) n.473G>T | ClinVar COSMIC |
11 | g.36575630C= | CA1964167703 | RAG1,RAG2 | c.2326C= (p.Arg776=) n.473G= | |
11 | g.36575630C>G | CA380154477 | RAG1,RAG2 | c.2326C>G (p.Arg776Gly) n.473G>C | |
11 | g.36575630C>T | CA122925 | RAG1,RAG2 | c.2326C>T (p.Arg776Trp) n.473G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.36575631G>A | CA380154478 | RAG1,RAG2 | c.2327G>A (p.Arg776Gln) n.472C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
11 | g.36575631G>C | CA380154479 | RAG1,RAG2 | c.2327G>C (p.Arg776Pro) n.472C>G | |
11 | g.36575631G= | CA1964167716 | RAG1,RAG2 | c.2327G= (p.Arg776=) n.472C= | |
11 | g.36575631G>T | CA380154480 | RAG1,RAG2 | c.2327G>T (p.Arg776Leu) n.472C>A | COSMIC |
11 | g.36575632G>A | CA474032428 | RAG1,RAG2 | c.2328G>A (p.Arg776=) n.471C>T | |
11 | g.36575632G>C | CA474032429 | RAG1,RAG2 | c.2328G>C (p.Arg776=) n.471C>G | |
11 | g.36575632G>T | CA474032430 | RAG1,RAG2 | c.2328G>T (p.Arg776=) n.471C>A | |
11 | g.36575633G>A | CA380154483 | RAG1,RAG2 | c.2329G>A (p.Asp777Asn) n.470C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575633G>C | CA380154481 | RAG1,RAG2 | c.2329G>C (p.Asp777His) n.470C>G | |
11 | g.36575633G= | CA1964167718 | RAG1,RAG2 | c.2329G= (p.Asp777=) n.470C= | |
11 | g.36575633G>T | CA380154482 | RAG1,RAG2 | c.2329G>T (p.Asp777Tyr) n.470C>A | |
11 | g.36575634A= | CA1964167723 | RAG1,RAG2 | c.2330A= (p.Asp777=) n.469T= | |
11 | g.36575634A>C | CA380154484 | RAG1,RAG2 | c.2330A>C (p.Asp777Ala) n.469T>G | |
11 | g.36575634A>G | CA380154485 | RAG1,RAG2 | c.2330A>G (p.Asp777Gly) n.469T>C | |
11 | g.36575634A>T | CA220601505 | RAG1,RAG2 | c.2330A>T (p.Asp777Val) n.469T>A | dbSNP |
11 | g.36575635T>A | CA380154486 | RAG1,RAG2 | c.2331T>A (p.Asp777Glu) n.468A>T | |
11 | g.36575635T>C | CA474032431 | RAG1,RAG2 | c.2331T>C (p.Asp777=) n.468A>G | |
11 | g.36575635T>G | CA380154487 | RAG1,RAG2 | c.2331T>G (p.Asp777Glu) n.468A>C | |
11 | g.36575636C>A | CA5950250 | RAG1,RAG2 | c.2332C>A (p.Arg778=) n.467G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575636C= | CA1964167734 | RAG1,RAG2 | c.2332C= (p.Arg778=) n.467G= | |
11 | g.36575636C>G | CA380154488 | RAG1,RAG2 | c.2332C>G (p.Arg778Gly) n.467G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575636C>T | CA380154489 | RAG1,RAG2 | c.2332C>T (p.Arg778Trp) n.467G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575637G>A | CA122916 | RAG1,RAG2 | c.2333G>A (p.Arg778Gln) n.466C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
11 | g.36575637G>C | CA380154490 | RAG1,RAG2 | c.2333G>C (p.Arg778Pro) n.466C>G | dbSNP |
11 | g.36575637G= | CA1964167743 | RAG1,RAG2 | c.2333G= (p.Arg778=) n.466C= | |
11 | g.36575637G>T | CA380154491 | RAG1,RAG2 | c.2333G>T (p.Arg778Leu) n.466C>A | |
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 |
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 |
11 | g.36575666A= | CA1964167783 | RAG1,RAG2 | c.2362A= (p.Ile788=) n.437T= | |
11 | g.36575666A>C | CA380154550 | RAG1,RAG2 | c.2362A>C (p.Ile788Leu) n.437T>G | |
11 | g.36575666A>G | CA5950253 | RAG1,RAG2 | c.2362A>G (p.Ile788Val) n.437T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.36575666A>T | CA380154551 | RAG1,RAG2 | c.2362A>T (p.Ile788Phe) n.437T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575667T>A | CA380154553 | RAG1,RAG2 | c.2363T>A (p.Ile788Asn) n.436A>T | |
11 | g.36575667T>C | CA380154554 | RAG1,RAG2 | c.2363T>C (p.Ile788Thr) n.436A>G | gnomAD v4 |
11 | g.36575667T>G | CA380154552 | RAG1,RAG2 | c.2363T>G (p.Ile788Ser) n.436A>C | |
11 | g.36575668T>A | CA474032454 | RAG1,RAG2 | c.2364T>A (p.Ile788=) n.435A>T | |
11 | g.36575668T>C | CA474032455 | RAG1,RAG2 | c.2364T>C (p.Ile788=) n.435A>G | |
11 | g.36575668T>G | CA380154555 | RAG1,RAG2 | c.2364T>G (p.Ile788Met) n.435A>C | |
11 | g.36575669G>A | CA380154556 | RAG1,RAG2 | c.2365G>A (p.Glu789Lys) n.434C>T | dbSNP gnomAD v2 |
11 | g.36575669G>C | CA380154557 | RAG1,RAG2 | c.2365G>C (p.Glu789Gln) n.434C>G | |
11 | g.36575669G= | CA1964167787 | RAG1,RAG2 | c.2365G= (p.Glu789=) n.434C= | |
11 | g.36575669G>T | CA380154558 | RAG1,RAG2 | c.2365G>T (p.Glu789Ter) n.434C>A | |
11 | g.36575670A>C | CA380154559 | RAG1,RAG2 | c.2366A>C (p.Glu789Ala) n.433T>G | |
11 | g.36575670A>G | CA380154560 | RAG1,RAG2 | c.2366A>G (p.Glu789Gly) n.433T>C | |
11 | g.36575670A>T | CA380154561 | RAG1,RAG2 | c.2366A>T (p.Glu789Val) n.433T>A | |
11 | g.36575671G>A | CA474032457 | RAG1,RAG2 | c.2367G>A (p.Glu789=) n.432C>T | |
11 | g.36575671G>C | CA380154562 | RAG1,RAG2 | c.2367G>C (p.Glu789Asp) n.432C>G | |
11 | g.36575671G>T | CA380154563 | RAG1,RAG2 | c.2367G>T (p.Glu789Asp) n.432C>A | |
11 | g.36575672A>C | CA380154564 | RAG1,RAG2 | c.2368A>C (p.Thr790Pro) n.431T>G | |
11 | g.36575672A>G | CA380154565 | RAG1,RAG2 | c.2368A>G (p.Thr790Ala) n.431T>C | |
11 | g.36575672A>T | CA380154566 | RAG1,RAG2 | c.2368A>T (p.Thr790Ser) n.431T>A | |
11 | g.36575673C>A | CA380154569 | RAG1,RAG2 | c.2369C>A (p.Thr790Lys) n.430G>T | |
11 | g.36575673C= | CA1964167805 | RAG1,RAG2 | c.2369C= (p.Thr790=) n.430G= | |
11 | g.36575673C>G | CA380154567 | RAG1,RAG2 | c.2369C>G (p.Thr790Arg) n.430G>C | |
11 | g.36575673C>T | CA380154568 | RAG1,RAG2 | c.2369C>T (p.Thr790Ile) n.430G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.36575674A>C | CA474032460 | RAG1,RAG2 | c.2370A>C (p.Thr790=) n.429T>G | |
11 | g.36575674A>G | CA474032461 | RAG1,RAG2 | c.2370A>G (p.Thr790=) n.429T>C | gnomAD v4 |
11 | g.36575674A>T | CA474032462 | RAG1,RAG2 | c.2370A>T (p.Thr790=) n.429T>A | |
11 | g.36575675G>A | CA380154570 | RAG1,RAG2 | c.2371G>A (p.Val791Ile) n.428C>T | |
11 | g.36575675G>C | CA380154571 | RAG1,RAG2 | c.2371G>C (p.Val791Leu) n.428C>G | |
11 | g.36575675G>T | CA380154572 | RAG1,RAG2 | c.2371G>T (p.Val791Phe) n.428C>A | |
11 | g.36575676T>A | CA380154573 | RAG1,RAG2 | c.2372T>A (p.Val791Asp) n.427A>T | gnomAD v4 |
11 | g.36575676T>C | CA380154574 | RAG1,RAG2 | c.2372T>C (p.Val791Ala) n.427A>G | |
11 | g.36575676T>G | CA380154575 | RAG1,RAG2 | c.2372T>G (p.Val791Gly) n.427A>C | |
11 | g.36575677C>A | CA474032465 | RAG1,RAG2 | c.2373C>A (p.Val791=) n.426G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.36575677C= | CA1964167809 | RAG1,RAG2 | c.2373C= (p.Val791=) n.426G= | |
11 | g.36575677C>G | CA474032466 | RAG1,RAG2 | c.2373C>G (p.Val791=) n.426G>C | dbSNP |
11 | g.36575677C>T | CA474032467 | RAG1,RAG2 | c.2373C>T (p.Val791=) n.426G>A | |
11 | g.36575678C>A | CA380154576 | RAG1,RAG2 | c.2374C>A (p.Pro792Thr) n.425G>T | |
11 | g.36575678C= | CA1964167814 | RAG1,RAG2 | c.2374C= (p.Pro792=) n.425G= | |
11 | g.36575678C>G | CA380154577 | RAG1,RAG2 | c.2374C>G (p.Pro792Ala) n.425G>C | |
11 | g.36575678C>T | CA220601542 | RAG1,RAG2 | c.2374C>T (p.Pro792Ser) n.425G>A | dbSNP gnomAD v4 |
11 | g.36575679C>A | CA380154578 | RAG1,RAG2 | c.2375C>A (p.Pro792His) n.424G>T | |
11 | g.36575679C>G | CA380154579 | RAG1,RAG2 | c.2375C>G (p.Pro792Arg) n.424G>C | |
11 | g.36575679C>T | CA380154580 | RAG1,RAG2 | c.2375C>T (p.Pro792Leu) n.424G>A | COSMIC |
11 | g.36575680T>A | CA474032470 | RAG1,RAG2 | c.2376T>A (p.Pro792=) n.423A>T | ClinVar dbSNP |
11 | g.36575680T>C | CA474032471 | RAG1,RAG2 | c.2376T>C (p.Pro792=) n.423A>G | |
11 | g.36575680T>G | CA474032472 | RAG1,RAG2 | c.2376T>G (p.Pro792=) n.423A>C | |
11 | g.36575681T>A | CA380154582 | RAG1,RAG2 | c.2377T>A (p.Ser793Thr) n.422A>T | |
11 | g.36575681T>C | CA380154583 | RAG1,RAG2 | c.2377T>C (p.Ser793Pro) n.422A>G | |
11 | g.36575681T>G | CA380154581 | RAG1,RAG2 | c.2377T>G (p.Ser793Ala) n.422A>C | |
11 | g.36575682C>A | CA380154586 | RAG1,RAG2 | c.2378C>A (p.Ser793Tyr) n.421G>T | |
11 | g.36575682C>G | CA380154584 | RAG1,RAG2 | c.2378C>G (p.Ser793Cys) n.421G>C | |
11 | g.36575682C>T | CA380154585 | RAG1,RAG2 | c.2378C>T (p.Ser793Phe) n.421G>A | |
11 | g.36575683C>A | CA474032476 | RAG1,RAG2 | c.2379C>A (p.Ser793=) n.420G>T | |
11 | g.36575683C>G | CA474032477 | RAG1,RAG2 | c.2379C>G (p.Ser793=) n.420G>C | |
11 | g.36575683C>T | CA474032478 | RAG1,RAG2 | c.2379C>T (p.Ser793=) n.420G>A | COSMIC |
11 | g.36575684A>C | CA380154587 | RAG1,RAG2 | c.2380A>C (p.Ile794Leu) n.419T>G | |
11 | g.36575684A>G | CA380154588 | RAG1,RAG2 | c.2380A>G (p.Ile794Val) n.419T>C | |
11 | g.36575684A>T | CA380154589 | RAG1,RAG2 | c.2380A>T (p.Ile794Leu) n.419T>A |