Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.36575322_36575995delinsGCGCA2740093700RAG1c.2018_2691delinsGCG (p.Ala673GlyfsTer7)
ClinVar
11g.36575584T>ACA380154378RAG1,RAG2c.2280T>A (p.Tyr760Ter)
n.519A>T
11g.36575584T>CCA474032402RAG1,RAG2c.2280T>C (p.Tyr760=)
n.519A>G
11g.36575584T>GCA380154379RAG1,RAG2c.2280T>G (p.Tyr760Ter)
n.519A>C
11g.36575585G>ACA380154380RAG1,RAG2c.2281G>A (p.Glu761Lys)
n.518C>T
11g.36575585G>CCA380154382RAG1,RAG2c.2281G>C (p.Glu761Gln)
n.518C>G
11g.36575585G>TCA380154381RAG1,RAG2c.2281G>T (p.Glu761Ter)
n.518C>A
11g.36575586A>CCA380154383RAG1,RAG2c.2282A>C (p.Glu761Ala)
n.517T>G
11g.36575586A>GCA380154384RAG1,RAG2c.2282A>G (p.Glu761Gly)
n.517T>C
11g.36575586A>TCA380154385RAG1,RAG2c.2282A>T (p.Glu761Val)
n.517T>A
11g.36575587G>ACA474032403RAG1,RAG2c.2283G>A (p.Glu761=)
n.516C>T
11g.36575587G>CCA380154386RAG1,RAG2c.2283G>C (p.Glu761Asp)
n.516C>G
11g.36575587G>TCA380154387RAG1,RAG2c.2283G>T (p.Glu761Asp)
n.516C>A
11g.36575588G>ACA5950241RAG1,RAG2c.2284G>A (p.Val762Ile)
n.515C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575588G>CCA380154388RAG1,RAG2c.2284G>C (p.Val762Leu)
n.515C>G
11g.36575588G=CA1964167611RAG1,RAG2c.2284G= (p.Val762=)
n.515C=
11g.36575588G>TCA380154389RAG1,RAG2c.2284G>T (p.Val762Phe)
n.515C>A
11g.36575589T>ACA380154390RAG1,RAG2c.2285T>A (p.Val762Asp)
n.514A>T
11g.36575589T>CCA380154391RAG1,RAG2c.2285T>C (p.Val762Ala)
n.514A>G
11g.36575589T>GCA380154392RAG1,RAG2c.2285T>G (p.Val762Gly)
n.514A>C
11g.36575590C>ACA474032404RAG1,RAG2c.2286C>A (p.Val762=)
n.513G>T
11g.36575590C=CA1964167614RAG1,RAG2c.2286C= (p.Val762=)
n.513G=
11g.36575590C>GCA5950242RAG1,RAG2c.2286C>G (p.Val762=)
n.513G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575590C>TCA474032405RAG1,RAG2c.2286C>T (p.Val762=)
n.513G>A
dbSNP
11g.36575591T>ACA380154395RAG1,RAG2c.2287T>A (p.Trp763Arg)
n.512A>T
11g.36575591T>CCA380154394RAG1,RAG2c.2287T>C (p.Trp763Arg)
n.512A>G
11g.36575591T>GCA380154393RAG1,RAG2c.2287T>G (p.Trp763Gly)
n.512A>C
11g.36575592G>ACA380154396RAG1,RAG2c.2288G>A (p.Trp763Ter)
n.511C>T
11g.36575592G>CCA380154397RAG1,RAG2c.2288G>C (p.Trp763Ser)
n.511C>G
11g.36575592G>TCA380154398RAG1,RAG2c.2288G>T (p.Trp763Leu)
n.511C>A
11g.36575593G>ACA380154399RAG1,RAG2c.2289G>A (p.Trp763Ter)
n.510C>T
11g.36575593G>CCA380154400RAG1,RAG2c.2289G>C (p.Trp763Cys)
n.510C>G
11g.36575593G>TCA380154401RAG1,RAG2c.2289G>T (p.Trp763Cys)
n.510C>A
11g.36575594C>ACA380154402RAG1,RAG2c.2290C>A (p.Arg764Ser)
n.509G>T
gnomAD v4
11g.36575594C=CA1964167617RAG1,RAG2c.2290C= (p.Arg764=)
n.509G=
11g.36575594C>GCA380154403RAG1,RAG2c.2290C>G (p.Arg764Gly)
n.509G>C
gnomAD v4
11g.36575594C>TCA380154404RAG1,RAG2c.2290C>T (p.Arg764Cys)
n.509G>A
dbSNP gnomAD v2 gnomAD v4 COSMIC
11g.36575595G>ACA5950243RAG1,RAG2c.2291G>A (p.Arg764His)
n.508C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.36575595G>CCA380154405RAG1,RAG2c.2291G>C (p.Arg764Pro)
n.508C>G
11g.36575595G=CA1964167622RAG1,RAG2c.2291G= (p.Arg764=)
n.508C=
11g.36575595G>TCA380154406RAG1,RAG2c.2291G>T (p.Arg764Leu)
n.508C>A
COSMIC
11g.36575596T>ACA474032406RAG1,RAG2c.2292T>A (p.Arg764=)
n.507A>T
11g.36575596T>CCA474032407RAG1,RAG2c.2292T>C (p.Arg764=)
n.507A>G
11g.36575596T>GCA474032408RAG1,RAG2c.2292T>G (p.Arg764=)
n.507A>C
11g.36575597T>ACA380154409RAG1,RAG2c.2293T>A (p.Ser765Thr)
n.506A>T
ClinVar
11g.36575597T>CCA380154408RAG1,RAG2c.2293T>C (p.Ser765Pro)
n.506A>G
11g.36575597T>GCA380154407RAG1,RAG2c.2293T>G (p.Ser765Ala)
n.506A>C
11g.36575598C>ACA380154410RAG1,RAG2c.2294C>A (p.Ser765Tyr)
n.505G>T
11g.36575598C>GCA380154412RAG1,RAG2c.2294C>G (p.Ser765Cys)
n.505G>C
11g.36575598C>TCA380154411RAG1,RAG2c.2294C>T (p.Ser765Phe)
n.505G>A
11g.36575599C>ACA474032409RAG1,RAG2c.2295C>A (p.Ser765=)
n.504G>T
11g.36575599C>GCA474032410RAG1,RAG2c.2295C>G (p.Ser765=)
n.504G>C
11g.36575599C>TCA474032411RAG1,RAG2c.2295C>T (p.Ser765=)
n.504G>A
11g.36575600A>CCA380154413RAG1,RAG2c.2296A>C (p.Asn766His)
n.503T>G
11g.36575600A>GCA380154415RAG1,RAG2c.2296A>G (p.Asn766Asp)
n.503T>C
11g.36575600A>TCA380154414RAG1,RAG2c.2296A>T (p.Asn766Tyr)
n.503T>A
11g.36575601A=CA1964167625RAG1,RAG2c.2297A= (p.Asn766=)
n.502T=
11g.36575601A>CCA380154416RAG1,RAG2c.2297A>C (p.Asn766Thr)
n.502T>G
11g.36575601A>GCA380154418RAG1,RAG2c.2297A>G (p.Asn766Ser)
n.502T>C
11g.36575601A>TCA380154417RAG1,RAG2c.2297A>T (p.Asn766Ile)
n.502T>A
dbSNP gnomAD v4
11g.36575602C>ACA380154419RAG1,RAG2c.2298C>A (p.Asn766Lys)
n.501G>T
11g.36575602C>GCA380154420RAG1,RAG2c.2298C>G (p.Asn766Lys)
n.501G>C
11g.36575602C>TCA474032412RAG1,RAG2c.2298C>T (p.Asn766=)
n.501G>A
11g.36575603C>ACA380154421RAG1,RAG2c.2299C>A (p.Pro767Thr)
n.500G>T
gnomAD v4
11g.36575603C>GCA380154422RAG1,RAG2c.2299C>G (p.Pro767Ala)
n.500G>C
11g.36575603C>TCA380154423RAG1,RAG2c.2299C>T (p.Pro767Ser)
n.500G>A
gnomAD v4
11g.36575604C>ACA380154424RAG1,RAG2c.2300C>A (p.Pro767His)
n.499G>T
11g.36575604C=CA1964167630RAG1,RAG2c.2300C= (p.Pro767=)
n.499G=
11g.36575604C>GCA380154425RAG1,RAG2c.2300C>G (p.Pro767Arg)
n.499G>C
dbSNP gnomAD v2 gnomAD v4
11g.36575604C>TCA380154426RAG1,RAG2c.2300C>T (p.Pro767Leu)
n.499G>A
gnomAD v4
11g.36575605T>ACA474032413RAG1,RAG2c.2301T>A (p.Pro767=)
n.498A>T
11g.36575605T>CCA474032414RAG1,RAG2c.2301T>C (p.Pro767=)
n.498A>G
11g.36575605T>GCA474032415RAG1,RAG2c.2301T>G (p.Pro767=)
n.498A>C
11g.36575606T>ACA380154427RAG1,RAG2c.2302T>A (p.Tyr768Asn)
n.497A>T
11g.36575606T>CCA380154428RAG1,RAG2c.2302T>C (p.Tyr768His)
n.497A>G
11g.36575606T>GCA380154429RAG1,RAG2c.2302T>G (p.Tyr768Asp)
n.497A>C
11g.36575607A>CCA380154432RAG1,RAG2c.2303A>C (p.Tyr768Ser)
n.496T>G
11g.36575607A>GCA380154431RAG1,RAG2c.2303A>G (p.Tyr768Cys)
n.496T>C
11g.36575607A>TCA380154430RAG1,RAG2c.2303A>T (p.Tyr768Phe)
n.496T>A
11g.36575608C>ACA380154433RAG1,RAG2c.2304C>A (p.Tyr768Ter)
n.495G>T
gnomAD v4
11g.36575608C=CA1964167633RAG1,RAG2c.2304C= (p.Tyr768=)
n.495G=
11g.36575608C>GCA380154434RAG1,RAG2c.2304C>G (p.Tyr768Ter)
n.495G>C
11g.36575608C>TCA5950244RAG1,RAG2c.2304C>T (p.Tyr768=)
n.495G>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575609C>ACA380154435RAG1,RAG2c.2305C>A (p.His769Asn)
n.494G>T
11g.36575609C>GCA380154436RAG1,RAG2c.2305C>G (p.His769Asp)
n.494G>C
11g.36575609C>TCA380154437RAG1,RAG2c.2305C>T (p.His769Tyr)
n.494G>A
11g.36575610A=CA1964167636RAG1,RAG2c.2306A= (p.His769=)
n.493T=
11g.36575610A>CCA380154438RAG1,RAG2c.2306A>C (p.His769Pro)
n.493T>G
11g.36575610A>GCA220601462RAG1,RAG2c.2306A>G (p.His769Arg)
n.493T>C
ClinVar dbSNP gnomAD v4
11g.36575610A>TCA380154439RAG1,RAG2c.2306A>T (p.His769Leu)
n.493T>A
11g.36575611T>ACA380154440RAG1,RAG2c.2307T>A (p.His769Gln)
n.492A>T
11g.36575611T>CCA474032416RAG1,RAG2c.2307T>C (p.His769=)
n.492A>G
ClinVar gnomAD v4
11g.36575611T>GCA380154441RAG1,RAG2c.2307T>G (p.His769Gln)
n.492A>C
11g.36575612G>ACA220601466RAG1,RAG2c.2308G>A (p.Glu770Lys)
n.491C>T
dbSNP COSMIC
11g.36575612G>CCA380154443RAG1,RAG2c.2308G>C (p.Glu770Gln)
n.491C>G
11g.36575612G=CA1964167642RAG1,RAG2c.2308G= (p.Glu770=)
n.491C=
11g.36575612G>TCA380154442RAG1,RAG2c.2308G>T (p.Glu770Ter)
n.491C>A
11g.36575613A>CCA380154444RAG1,RAG2c.2309A>C (p.Glu770Ala)
n.490T>G
11g.36575613A>GCA380154445RAG1,RAG2c.2309A>G (p.Glu770Gly)
n.490T>C
11g.36575613A>TCA380154446RAG1,RAG2c.2309A>T (p.Glu770Val)
n.490T>A
11g.36575614G>ACA220601470RAG1,RAG2c.2310G>A (p.Glu770=)
n.489C>T
dbSNP gnomAD v2 gnomAD v4
11g.36575614G>CCA380154447RAG1,RAG2c.2310G>C (p.Glu770Asp)
n.489C>G
ClinVar
11g.36575614G=CA1964167647RAG1,RAG2c.2310G= (p.Glu770=)
n.489C=
11g.36575614G>TCA380154448RAG1,RAG2c.2310G>T (p.Glu770Asp)
n.489C>A
11g.36575615T>ACA5950245RAG1,RAG2c.2311T>A (p.Ser771Thr)
n.488A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575615T>CCA380154449RAG1,RAG2c.2311T>C (p.Ser771Pro)
n.488A>G
dbSNP gnomAD v2 gnomAD v4
11g.36575615T>GCA380154450RAG1,RAG2c.2311T>G (p.Ser771Ala)
n.488A>C
11g.36575615T=CA1964167654RAG1,RAG2c.2311T= (p.Ser771=)
n.488A=
11g.36575616C>ACA380154451RAG1,RAG2c.2312C>A (p.Ser771Tyr)
n.487G>T
gnomAD v4
11g.36575616C>GCA380154452RAG1,RAG2c.2312C>G (p.Ser771Cys)
n.487G>C
gnomAD v4
11g.36575616C>TCA380154453RAG1,RAG2c.2312C>T (p.Ser771Phe)
n.487G>A
11g.36575617T>ACA474032418RAG1,RAG2c.2313T>A (p.Ser771=)
n.486A>T
11g.36575617T>CCA220601486RAG1,RAG2c.2313T>C (p.Ser771=)
n.486A>G
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.36575617T>GCA474032417RAG1,RAG2c.2313T>G (p.Ser771=)
n.486A>C
11g.36575617T=CA1964167657RAG1,RAG2c.2313T= (p.Ser771=)
n.486A=
11g.36575618G>ACA380154454RAG1,RAG2c.2314G>A (p.Val772Met)
n.485C>T
gnomAD v4
11g.36575618G>CCA380154456RAG1,RAG2c.2314G>C (p.Val772Leu)
n.485C>G
gnomAD v4
11g.36575618G>TCA380154455RAG1,RAG2c.2314G>T (p.Val772Leu)
n.485C>A
11g.36575619T>ACA380154457RAG1,RAG2c.2315T>A (p.Val772Glu)
n.484A>T
11g.36575619T>CCA380154458RAG1,RAG2c.2315T>C (p.Val772Ala)
n.484A>G
dbSNP gnomAD v3 gnomAD v4
11g.36575619T>GCA380154459RAG1,RAG2c.2315T>G (p.Val772Gly)
n.484A>C
11g.36575619T=CA1964167665RAG1,RAG2c.2315T= (p.Val772=)
n.484A=
11g.36575619_36575620delinsTGCA1964167670RAG1,RAG2c.2315_2316delinsTG (p.Val772=)
n.483_484delinsCA
11g.36575620G>ACA474032419RAG1,RAG2c.2316G>A (p.Val772=)
n.483C>T
11g.36575620G>CCA474032420RAG1,RAG2c.2316G>C (p.Val772=)
n.483C>G
11g.36575620G>TCA474032421RAG1,RAG2c.2316G>T (p.Val772=)
n.483C>A
11g.36575621delCA1964167673RAG1,RAG2c.2317del (p.Glu773LysfsTer7)
n.483del
dbSNP
11g.36575621G>ACA380154460RAG1,RAG2c.2317G>A (p.Glu773Lys)
n.482C>T
11g.36575621G>CCA380154461RAG1,RAG2c.2317G>C (p.Glu773Gln)
n.482C>G
11g.36575621G>TCA380154462RAG1,RAG2c.2317G>T (p.Glu773Ter)
n.482C>A
11g.36575622A=CA1964167677RAG1,RAG2c.2318A= (p.Glu773=)
n.481T=
11g.36575622A>CCA380154463RAG1,RAG2c.2318A>C (p.Glu773Ala)
n.481T>G
11g.36575622A>GCA5950246RAG1,RAG2c.2318A>G (p.Glu773Gly)
n.481T>C
dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575622A>TCA380154464RAG1,RAG2c.2318A>T (p.Glu773Val)
n.481T>A
11g.36575623A>CCA380154465RAG1,RAG2c.2319A>C (p.Glu773Asp)
n.480T>G
11g.36575623A>GCA474032422RAG1,RAG2c.2319A>G (p.Glu773=)
n.480T>C
11g.36575623A>TCA380154466RAG1,RAG2c.2319A>T (p.Glu773Asp)
n.480T>A
11g.36575624G>ACA5950247RAG1,RAG2c.2320G>A (p.Glu774Lys)
n.479C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575624G>CCA380154467RAG1,RAG2c.2320G>C (p.Glu774Gln)
n.479C>G
11g.36575624G=CA1964167682RAG1,RAG2c.2320G= (p.Glu774=)
n.479C=
11g.36575624G>TCA122877RAG1,RAG2c.2320G>T (p.Glu774Ter)
n.479C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.36575625A>CCA380154469RAG1,RAG2c.2321A>C (p.Glu774Ala)
n.478T>G
11g.36575625A>GCA380154468RAG1,RAG2c.2321A>G (p.Glu774Gly)
n.478T>C
11g.36575625A>TCA380154470RAG1,RAG2c.2321A>T (p.Glu774Val)
n.478T>A
11g.36575626A>CCA380154471RAG1,RAG2c.2322A>C (p.Glu774Asp)
n.477T>G
11g.36575626A>GCA474032423RAG1,RAG2c.2322A>G (p.Glu774=)
n.477T>C
11g.36575626A>TCA380154472RAG1,RAG2c.2322A>T (p.Glu774Asp)
n.477T>A
11g.36575627C>ACA380154473RAG1,RAG2c.2323C>A (p.Leu775Met)
n.476G>T
11g.36575627C>GCA380154474RAG1,RAG2c.2323C>G (p.Leu775Val)
n.476G>C
11g.36575627C>TCA474032424RAG1,RAG2c.2323C>T (p.Leu775=)
n.476G>A
11g.36575628T>ACA380154475RAG1,RAG2c.2324T>A (p.Leu775Gln)
n.475A>T
11g.36575628T>CCA380154476RAG1,RAG2c.2324T>C (p.Leu775Pro)
n.475A>G
11g.36575628T>GCA5950248RAG1,RAG2c.2324T>G (p.Leu775Arg)
n.475A>C
dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575628T=CA1964167690RAG1,RAG2c.2324T= (p.Leu775=)
n.475A=
11g.36575629G>ACA5950249RAG1,RAG2c.2325G>A (p.Leu775=)
n.474C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575629G>CCA474032426RAG1,RAG2c.2325G>C (p.Leu775=)
n.474C>G
11g.36575629G=CA1964167694RAG1,RAG2c.2325G= (p.Leu775=)
n.474C=
11g.36575629G>TCA474032425RAG1,RAG2c.2325G>T (p.Leu775=)
n.474C>A
11g.36575630C>ACA474032427RAG1,RAG2c.2326C>A (p.Arg776=)
n.473G>T
ClinVar COSMIC
11g.36575630C=CA1964167703RAG1,RAG2c.2326C= (p.Arg776=)
n.473G=
11g.36575630C>GCA380154477RAG1,RAG2c.2326C>G (p.Arg776Gly)
n.473G>C
11g.36575630C>TCA122925RAG1,RAG2c.2326C>T (p.Arg776Trp)
n.473G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.36575631G>ACA380154478RAG1,RAG2c.2327G>A (p.Arg776Gln)
n.472C>T
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
11g.36575631G>CCA380154479RAG1,RAG2c.2327G>C (p.Arg776Pro)
n.472C>G
11g.36575631G=CA1964167716RAG1,RAG2c.2327G= (p.Arg776=)
n.472C=
11g.36575631G>TCA380154480RAG1,RAG2c.2327G>T (p.Arg776Leu)
n.472C>A
COSMIC
11g.36575632G>ACA474032428RAG1,RAG2c.2328G>A (p.Arg776=)
n.471C>T
11g.36575632G>CCA474032429RAG1,RAG2c.2328G>C (p.Arg776=)
n.471C>G
11g.36575632G>TCA474032430RAG1,RAG2c.2328G>T (p.Arg776=)
n.471C>A
11g.36575633G>ACA380154483RAG1,RAG2c.2329G>A (p.Asp777Asn)
n.470C>T
dbSNP gnomAD v2 gnomAD v4
11g.36575633G>CCA380154481RAG1,RAG2c.2329G>C (p.Asp777His)
n.470C>G
11g.36575633G=CA1964167718RAG1,RAG2c.2329G= (p.Asp777=)
n.470C=
11g.36575633G>TCA380154482RAG1,RAG2c.2329G>T (p.Asp777Tyr)
n.470C>A
11g.36575634A=CA1964167723RAG1,RAG2c.2330A= (p.Asp777=)
n.469T=
11g.36575634A>CCA380154484RAG1,RAG2c.2330A>C (p.Asp777Ala)
n.469T>G
11g.36575634A>GCA380154485RAG1,RAG2c.2330A>G (p.Asp777Gly)
n.469T>C
11g.36575634A>TCA220601505RAG1,RAG2c.2330A>T (p.Asp777Val)
n.469T>A
dbSNP
11g.36575635T>ACA380154486RAG1,RAG2c.2331T>A (p.Asp777Glu)
n.468A>T
11g.36575635T>CCA474032431RAG1,RAG2c.2331T>C (p.Asp777=)
n.468A>G
11g.36575635T>GCA380154487RAG1,RAG2c.2331T>G (p.Asp777Glu)
n.468A>C
11g.36575636C>ACA5950250RAG1,RAG2c.2332C>A (p.Arg778=)
n.467G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575636C=CA1964167734RAG1,RAG2c.2332C= (p.Arg778=)
n.467G=
11g.36575636C>GCA380154488RAG1,RAG2c.2332C>G (p.Arg778Gly)
n.467G>C
dbSNP gnomAD v2 gnomAD v4
11g.36575636C>TCA380154489RAG1,RAG2c.2332C>T (p.Arg778Trp)
n.467G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.36575637G>ACA122916RAG1,RAG2c.2333G>A (p.Arg778Gln)
n.466C>T
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
11g.36575637G>CCA380154490RAG1,RAG2c.2333G>C (p.Arg778Pro)
n.466C>G
dbSNP
11g.36575637G=CA1964167743RAG1,RAG2c.2333G= (p.Arg778=)
n.466C=
11g.36575637G>TCA380154491RAG1,RAG2c.2333G>T (p.Arg778Leu)
n.466C>A
11g.36575638G>ACA474032434RAG1,RAG2c.2334G>A (p.Arg778=)
n.465C>T
11g.36575638G>CCA474032432RAG1,RAG2c.2334G>C (p.Arg778=)
n.465C>G
11g.36575638G>TCA474032433RAG1,RAG2c.2334G>T (p.Arg778=)
n.465C>A
11g.36575639G>ACA380154494RAG1,RAG2c.2335G>A (p.Val779Met)
n.464C>T
11g.36575639G>CCA380154493RAG1,RAG2c.2335G>C (p.Val779Leu)
n.464C>G
11g.36575639G>TCA380154492RAG1,RAG2c.2335G>T (p.Val779Leu)
n.464C>A
11g.36575640T>ACA380154495RAG1,RAG2c.2336T>A (p.Val779Glu)
n.463A>T
11g.36575640T>CCA380154496RAG1,RAG2c.2336T>C (p.Val779Ala)
n.463A>G
gnomAD v4
11g.36575640T>GCA380154497RAG1,RAG2c.2336T>G (p.Val779Gly)
n.463A>C
11g.36575641G>ACA474032435RAG1,RAG2c.2337G>A (p.Val779=)
n.462C>T
dbSNP gnomAD v2
11g.36575641G>CCA474032436RAG1,RAG2c.2337G>C (p.Val779=)
n.462C>G
11g.36575641G=CA1964167748RAG1,RAG2c.2337G= (p.Val779=)
n.462C=
11g.36575641G>TCA474032437RAG1,RAG2c.2337G>T (p.Val779=)
n.462C>A
11g.36575642A>CCA380154498RAG1,RAG2c.2338A>C (p.Lys780Gln)
n.461T>G
11g.36575642A>GCA380154499RAG1,RAG2c.2338A>G (p.Lys780Glu)
n.461T>C
11g.36575642A>TCA380154500RAG1,RAG2c.2338A>T (p.Lys780Ter)
n.461T>A
11g.36575643A>CCA380154503RAG1,RAG2c.2339A>C (p.Lys780Thr)
n.460T>G
11g.36575643A>GCA380154501RAG1,RAG2c.2339A>G (p.Lys780Arg)
n.460T>C
11g.36575643A>TCA380154502RAG1,RAG2c.2339A>T (p.Lys780Ile)
n.460T>A
11g.36575644A>CCA380154504RAG1,RAG2c.2340A>C (p.Lys780Asn)
n.459T>G
11g.36575644A>GCA474032438RAG1,RAG2c.2340A>G (p.Lys780=)
n.459T>C
11g.36575644A>TCA380154505RAG1,RAG2c.2340A>T (p.Lys780Asn)
n.459T>A
COSMIC
11g.36575645G>ACA380154506RAG1,RAG2c.2341G>A (p.Gly781Arg)
n.458C>T
11g.36575645G>CCA380154507RAG1,RAG2c.2341G>C (p.Gly781Arg)
n.458C>G
gnomAD v4
11g.36575645G>TCA380154508RAG1,RAG2c.2341G>T (p.Gly781Trp)
n.458C>A
gnomAD v4
11g.36575646G>ACA380154509RAG1,RAG2c.2342G>A (p.Gly781Glu)
n.457C>T
gnomAD v4
11g.36575646G>CCA380154511RAG1,RAG2c.2342G>C (p.Gly781Ala)
n.457C>G
11g.36575646G>TCA380154510RAG1,RAG2c.2342G>T (p.Gly781Val)
n.457C>A
11g.36575647G>ACA474032439RAG1,RAG2c.2343G>A (p.Gly781=)
n.456C>T
ClinVar dbSNP
11g.36575647G>CCA474032440RAG1,RAG2c.2343G>C (p.Gly781=)
n.456C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.36575647G=CA1964167749RAG1,RAG2c.2343G= (p.Gly781=)
n.456C=
11g.36575647G>TCA220601514RAG1,RAG2c.2343G>T (p.Gly781=)
n.456C>A
ClinVar dbSNP gnomAD v4
11g.36575648G>ACA380154512RAG1,RAG2c.2344G>A (p.Val782Ile)
n.455C>T
dbSNP
11g.36575648G>CCA380154513RAG1,RAG2c.2344G>C (p.Val782Leu)
n.455C>G
11g.36575648G>TCA380154514RAG1,RAG2c.2344G>T (p.Val782Phe)
n.455C>A
gnomAD v4
11g.36575649T>ACA220601518RAG1,RAG2c.2345T>A (p.Val782Asp)
n.454A>T
ClinVar dbSNP gnomAD v4
11g.36575649T>CCA380154515RAG1,RAG2c.2345T>C (p.Val782Ala)
n.454A>G
11g.36575649T>GCA380154516RAG1,RAG2c.2345T>G (p.Val782Gly)
n.454A>C
11g.36575649T=CA1964167753RAG1,RAG2c.2345T= (p.Val782=)
n.454A=
11g.36575650C>ACA474032441RAG1,RAG2c.2346C>A (p.Val782=)
n.453G>T
11g.36575650C>GCA474032442RAG1,RAG2c.2346C>G (p.Val782=)
n.453G>C
11g.36575650C>TCA474032443RAG1,RAG2c.2346C>T (p.Val782=)
n.453G>A
11g.36575651T>ACA380154517RAG1,RAG2c.2347T>A (p.Ser783Thr)
n.452A>T
11g.36575651T>CCA380154518RAG1,RAG2c.2347T>C (p.Ser783Pro)
n.452A>G
11g.36575651T>GCA380154519RAG1,RAG2c.2347T>G (p.Ser783Ala)
n.452A>C
11g.36575652C>ACA380154520RAG1,RAG2c.2348C>A (p.Ser783Ter)
n.451G>T
11g.36575652C=CA1964167759RAG1,RAG2c.2348C= (p.Ser783=)
n.451G=
11g.36575652C>GCA5950251RAG1,RAG2c.2348C>G (p.Ser783Ter)
n.451G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.36575652C>TCA380154521RAG1,RAG2c.2348C>T (p.Ser783Leu)
n.451G>A
dbSNP
11g.36575653A>CCA474032444RAG1,RAG2c.2349A>C (p.Ser783=)
n.450T>G
11g.36575653A>GCA474032445RAG1,RAG2c.2349A>G (p.Ser783=)
n.450T>C
11g.36575653A>TCA474032446RAG1,RAG2c.2349A>T (p.Ser783=)
n.450T>A
11g.36575654G>ACA380154523RAG1,RAG2c.2350G>A (p.Ala784Thr)
n.449C>T
11g.36575654G>CCA380154524RAG1,RAG2c.2350G>C (p.Ala784Pro)
n.449C>G
11g.36575654G>TCA380154522RAG1,RAG2c.2350G>T (p.Ala784Ser)
n.449C>A
gnomAD v4
11g.36575655C>ACA380154525RAG1,RAG2c.2351C>A (p.Ala784Asp)
n.448G>T
11g.36575655C>GCA380154527RAG1,RAG2c.2351C>G (p.Ala784Gly)
n.448G>C
11g.36575655C>TCA380154526RAG1,RAG2c.2351C>T (p.Ala784Val)
n.448G>A
gnomAD v4
11g.36575656T>ACA474032447RAG1,RAG2c.2352T>A (p.Ala784=)
n.447A>T
11g.36575656T>CCA474032448RAG1,RAG2c.2352T>C (p.Ala784=)
n.447A>G
11g.36575656T>GCA474032449RAG1,RAG2c.2352T>G (p.Ala784=)
n.447A>C
11g.36575657A>CCA380154528RAG1,RAG2c.2353A>C (p.Lys785Gln)
n.446T>G
11g.36575657A>GCA380154530RAG1,RAG2c.2353A>G (p.Lys785Glu)
n.446T>C
11g.36575657A>TCA380154529RAG1,RAG2c.2353A>T (p.Lys785Ter)
n.446T>A
11g.36575658A>CCA380154531RAG1,RAG2c.2354A>C (p.Lys785Thr)
n.445T>G
11g.36575658A>GCA380154532RAG1,RAG2c.2354A>G (p.Lys785Arg)
n.445T>C
11g.36575658A>TCA380154533RAG1,RAG2c.2354A>T (p.Lys785Ile)
n.445T>A
11g.36575659A>CCA380154534RAG1,RAG2c.2355A>C (p.Lys785Asn)
n.444T>G
11g.36575659A>GCA474032450RAG1,RAG2c.2355A>G (p.Lys785=)
n.444T>C
gnomAD v4
11g.36575659A>TCA380154535RAG1,RAG2c.2355A>T (p.Lys785Asn)
n.444T>A
11g.36575660C>ACA380154536RAG1,RAG2c.2356C>A (p.Pro786Thr)
n.443G>T
11g.36575660C=CA1964167768RAG1,RAG2c.2356C= (p.Pro786=)
n.443G=
11g.36575660C>GCA380154537RAG1,RAG2c.2356C>G (p.Pro786Ala)
n.443G>C
11g.36575660C>TCA380154538RAG1,RAG2c.2356C>T (p.Pro786Ser)
n.443G>A
dbSNP
11g.36575661C>ACA380154539RAG1,RAG2c.2357C>A (p.Pro786His)
n.442G>T
11g.36575661C=CA1964167771RAG1,RAG2c.2357C= (p.Pro786=)
n.442G=
11g.36575661C>GCA380154540RAG1,RAG2c.2357C>G (p.Pro786Arg)
n.442G>C
11g.36575661C>TCA380154541RAG1,RAG2c.2357C>T (p.Pro786Leu)
n.442G>A
dbSNP gnomAD v3 gnomAD v4
11g.36575662T>ACA474032451RAG1,RAG2c.2358T>A (p.Pro786=)
n.441A>T
11g.36575662T>CCA474032452RAG1,RAG2c.2358T>C (p.Pro786=)
n.441A>G
11g.36575662T>GCA474032453RAG1,RAG2c.2358T>G (p.Pro786=)
n.441A>C
11g.36575663T>ACA380154542RAG1,RAG2c.2359T>A (p.Phe787Ile)
n.440A>T
11g.36575663T>CCA380154544RAG1,RAG2c.2359T>C (p.Phe787Leu)
n.440A>G
gnomAD v4
11g.36575663T>GCA380154543RAG1,RAG2c.2359T>G (p.Phe787Val)
n.440A>C
11g.36575664T>ACA380154545RAG1,RAG2c.2360T>A (p.Phe787Tyr)
n.439A>T
11g.36575664T>CCA380154546RAG1,RAG2c.2360T>C (p.Phe787Ser)
n.439A>G
11g.36575664T>GCA380154547RAG1,RAG2c.2360T>G (p.Phe787Cys)
n.439A>C
11g.36575665C>ACA380154548RAG1,RAG2c.2361C>A (p.Phe787Leu)
n.438G>T
11g.36575665C=CA1964167775RAG1,RAG2c.2361C= (p.Phe787=)
n.438G=
11g.36575665C>GCA380154549RAG1,RAG2c.2361C>G (p.Phe787Leu)
n.438G>C
11g.36575665C>TCA5950252RAG1,RAG2c.2361C>T (p.Phe787=)
n.438G>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575666A=CA1964167783RAG1,RAG2c.2362A= (p.Ile788=)
n.437T=
11g.36575666A>CCA380154550RAG1,RAG2c.2362A>C (p.Ile788Leu)
n.437T>G
11g.36575666A>GCA5950253RAG1,RAG2c.2362A>G (p.Ile788Val)
n.437T>C
dbSNP ExAC gnomAD v2 gnomAD v4
11g.36575666A>TCA380154551RAG1,RAG2c.2362A>T (p.Ile788Phe)
n.437T>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.36575667T>ACA380154553RAG1,RAG2c.2363T>A (p.Ile788Asn)
n.436A>T
11g.36575667T>CCA380154554RAG1,RAG2c.2363T>C (p.Ile788Thr)
n.436A>G
gnomAD v4
11g.36575667T>GCA380154552RAG1,RAG2c.2363T>G (p.Ile788Ser)
n.436A>C
11g.36575668T>ACA474032454RAG1,RAG2c.2364T>A (p.Ile788=)
n.435A>T
11g.36575668T>CCA474032455RAG1,RAG2c.2364T>C (p.Ile788=)
n.435A>G
11g.36575668T>GCA380154555RAG1,RAG2c.2364T>G (p.Ile788Met)
n.435A>C
11g.36575669G>ACA380154556RAG1,RAG2c.2365G>A (p.Glu789Lys)
n.434C>T
dbSNP gnomAD v2
11g.36575669G>CCA380154557RAG1,RAG2c.2365G>C (p.Glu789Gln)
n.434C>G
11g.36575669G=CA1964167787RAG1,RAG2c.2365G= (p.Glu789=)
n.434C=
11g.36575669G>TCA380154558RAG1,RAG2c.2365G>T (p.Glu789Ter)
n.434C>A
11g.36575670A>CCA380154559RAG1,RAG2c.2366A>C (p.Glu789Ala)
n.433T>G
11g.36575670A>GCA380154560RAG1,RAG2c.2366A>G (p.Glu789Gly)
n.433T>C
11g.36575670A>TCA380154561RAG1,RAG2c.2366A>T (p.Glu789Val)
n.433T>A
11g.36575671G>ACA474032457RAG1,RAG2c.2367G>A (p.Glu789=)
n.432C>T
11g.36575671G>CCA380154562RAG1,RAG2c.2367G>C (p.Glu789Asp)
n.432C>G
11g.36575671G>TCA380154563RAG1,RAG2c.2367G>T (p.Glu789Asp)
n.432C>A
11g.36575672A>CCA380154564RAG1,RAG2c.2368A>C (p.Thr790Pro)
n.431T>G
11g.36575672A>GCA380154565RAG1,RAG2c.2368A>G (p.Thr790Ala)
n.431T>C
11g.36575672A>TCA380154566RAG1,RAG2c.2368A>T (p.Thr790Ser)
n.431T>A
11g.36575673C>ACA380154569RAG1,RAG2c.2369C>A (p.Thr790Lys)
n.430G>T
11g.36575673C=CA1964167805RAG1,RAG2c.2369C= (p.Thr790=)
n.430G=
11g.36575673C>GCA380154567RAG1,RAG2c.2369C>G (p.Thr790Arg)
n.430G>C
11g.36575673C>TCA380154568RAG1,RAG2c.2369C>T (p.Thr790Ile)
n.430G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.36575674A>CCA474032460RAG1,RAG2c.2370A>C (p.Thr790=)
n.429T>G
11g.36575674A>GCA474032461RAG1,RAG2c.2370A>G (p.Thr790=)
n.429T>C
gnomAD v4
11g.36575674A>TCA474032462RAG1,RAG2c.2370A>T (p.Thr790=)
n.429T>A
11g.36575675G>ACA380154570RAG1,RAG2c.2371G>A (p.Val791Ile)
n.428C>T
11g.36575675G>CCA380154571RAG1,RAG2c.2371G>C (p.Val791Leu)
n.428C>G
11g.36575675G>TCA380154572RAG1,RAG2c.2371G>T (p.Val791Phe)
n.428C>A
11g.36575676T>ACA380154573RAG1,RAG2c.2372T>A (p.Val791Asp)
n.427A>T
gnomAD v4
11g.36575676T>CCA380154574RAG1,RAG2c.2372T>C (p.Val791Ala)
n.427A>G
11g.36575676T>GCA380154575RAG1,RAG2c.2372T>G (p.Val791Gly)
n.427A>C
11g.36575677C>ACA474032465RAG1,RAG2c.2373C>A (p.Val791=)
n.426G>T
dbSNP gnomAD v2 gnomAD v4
11g.36575677C=CA1964167809RAG1,RAG2c.2373C= (p.Val791=)
n.426G=
11g.36575677C>GCA474032466RAG1,RAG2c.2373C>G (p.Val791=)
n.426G>C
dbSNP
11g.36575677C>TCA474032467RAG1,RAG2c.2373C>T (p.Val791=)
n.426G>A
11g.36575678C>ACA380154576RAG1,RAG2c.2374C>A (p.Pro792Thr)
n.425G>T
11g.36575678C=CA1964167814RAG1,RAG2c.2374C= (p.Pro792=)
n.425G=
11g.36575678C>GCA380154577RAG1,RAG2c.2374C>G (p.Pro792Ala)
n.425G>C
11g.36575678C>TCA220601542RAG1,RAG2c.2374C>T (p.Pro792Ser)
n.425G>A
dbSNP gnomAD v4
11g.36575679C>ACA380154578RAG1,RAG2c.2375C>A (p.Pro792His)
n.424G>T
11g.36575679C>GCA380154579RAG1,RAG2c.2375C>G (p.Pro792Arg)
n.424G>C
11g.36575679C>TCA380154580RAG1,RAG2c.2375C>T (p.Pro792Leu)
n.424G>A
COSMIC
11g.36575680T>ACA474032470RAG1,RAG2c.2376T>A (p.Pro792=)
n.423A>T
ClinVar dbSNP
11g.36575680T>CCA474032471RAG1,RAG2c.2376T>C (p.Pro792=)
n.423A>G
11g.36575680T>GCA474032472RAG1,RAG2c.2376T>G (p.Pro792=)
n.423A>C
11g.36575681T>ACA380154582RAG1,RAG2c.2377T>A (p.Ser793Thr)
n.422A>T
11g.36575681T>CCA380154583RAG1,RAG2c.2377T>C (p.Ser793Pro)
n.422A>G
11g.36575681T>GCA380154581RAG1,RAG2c.2377T>G (p.Ser793Ala)
n.422A>C
11g.36575682C>ACA380154586RAG1,RAG2c.2378C>A (p.Ser793Tyr)
n.421G>T
11g.36575682C>GCA380154584RAG1,RAG2c.2378C>G (p.Ser793Cys)
n.421G>C
11g.36575682C>TCA380154585RAG1,RAG2c.2378C>T (p.Ser793Phe)
n.421G>A
11g.36575683C>ACA474032476RAG1,RAG2c.2379C>A (p.Ser793=)
n.420G>T
11g.36575683C>GCA474032477RAG1,RAG2c.2379C>G (p.Ser793=)
n.420G>C
11g.36575683C>TCA474032478RAG1,RAG2c.2379C>T (p.Ser793=)
n.420G>A
COSMIC
11g.36575684A>CCA380154587RAG1,RAG2c.2380A>C (p.Ile794Leu)
n.419T>G
11g.36575684A>GCA380154588RAG1,RAG2c.2380A>G (p.Ile794Val)
n.419T>C
11g.36575684A>TCA380154589RAG1,RAG2c.2380A>T (p.Ile794Leu)
n.419T>A

Number of alleles fetched