Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47401439_47411294delCA331194 ClinVar
2g.47403280_47410368delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTCA658760387MSH2c.89_641delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
c.-30-80_443delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
n.161_713delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
n.151_703delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
2g.47408402_47410373delCA2581463448MSH2c.213_645+1del
c.15_447+1del
n.285_717+1del
n.275_707+1del
2g.47409413_47411458delCA331584MSH2c.367-681_646-956del
c.169-681_448-956del
n.439-681_718-956del
n.429-681_708-956del
 ClinVar
2g.47409567_47410219delinsTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGGCA2495830775MSH2c.367-527_492delinsTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGG
c.169-527_294delinsTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGG
n.439-527_564delinsTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGG
n.429-527_554delinsTTGGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACAGCACTCAGCCAGTTATTTTTTTATAAGAAAACATTTTACTGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGATTGAACCCTTGAGGCAGAGGTTGCAGTGAGTTGAGATCGCACCATTGCACTCTAGCCTGGGTGACAGAGCAAGACTTCATCTCAAAAAAAAGAGAAAACATTTTATTAATAAGGTTCATAGAGTTTGGATTTTTCCTTTTTGCTTATAAAATTTTAAAGTATGTTCAAGAGTTTGTTAAATTTTTAAAATTTTATTTTTACTTAGGCTTCTCCTGGCAATCTCTCTCAGTTTGAAGACATTCTCTTTGGTAACAATGATATGTCAGCTTCCATTGGTGTTGTGGGTGTTAAAATGTCCGCAGTTGATGGCCAGAGACAGGTTGGAGTTGGG
2g.47409569_47410220delCA658795727MSH2c.367-525_493del
c.169-525_295del
n.439-525_565del
n.429-525_555del
 ClinVar dbSNP
2g.47409628_47411030delCA331583MSH2c.367-466_645+658del
c.169-466_447+658del
n.439-466_717+658del
n.429-466_707+658del
 ClinVar
2g.47409642_47411692delCA331582MSH2c.367-452_646-722del
c.169-452_448-722del
n.439-452_718-722del
n.429-452_708-722del
 ClinVar
2g.47409723_47411901delCA331581MSH2c.367-371_646-513del
c.169-371_448-513del
n.439-371_718-513del
n.429-371_708-513del
 ClinVar
2g.47410080_47410088delinsTTATTTTTACA2495831107MSH2c.367-14_367-6delinsTTATTTTTA (n.367-14_367-6delinsTTATTTTTA)
c.169-14_169-6delinsTTATTTTTA (n.169-14_169-6delinsTTATTTTTA)
n.439-14_439-6delinsTTATTTTTA
n.429-14_429-6delinsTTATTTTTA
2g.47410081_47410088delinsAATTTTTCA16617556MSH2c.367-13_367-6delinsAATTTTT (n.367-13_367-6delinsAATTTTT)
c.169-13_169-6delinsAATTTTT (n.169-13_169-6delinsAATTTTT)
n.439-13_439-6delinsAATTTTT
n.429-13_429-6delinsAATTTTT
 ClinVar dbSNP
2g.47410083T>ACA2699274458MSH2c.367-11T>A (n.367-11T>A)
c.169-11T>A (n.169-11T>A)
n.439-11T>A
n.429-11T>A
 dbSNP
2g.47410083T>CCA2740092845MSH2c.367-11T>C (n.367-11T>C)
c.169-11T>C (n.169-11T>C)
n.439-11T>C
n.429-11T>C
 ClinVar
2g.47410084T>ACA2499216004MSH2c.367-10T>A (n.367-10T>A)
c.169-10T>A (n.169-10T>A)
n.439-10T>A
n.429-10T>A
 ClinVar dbSNP
2g.47410084T>GCA2573051951MSH2c.367-10T>G (n.367-10T>G)
c.169-10T>G (n.169-10T>G)
n.439-10T>G
n.429-10T>G
 ClinVar dbSNP
2g.47410086T>CCA2699274504MSH2c.367-8T>C (n.367-8T>C)
c.169-8T>C (n.169-8T>C)
n.439-8T>C
n.429-8T>C
 dbSNP
2g.47410088_47410097dupCA2586969160MSH2c.367-6_370dup
c.169-6_172dup
n.439-6_442dup
n.429-6_432dup
2g.47410087T>ACA2699274505MSH2c.367-7T>A (n.367-7T>A)
c.169-7T>A (n.169-7T>A)
n.439-7T>A
n.429-7T>A
 dbSNP
2g.47410087T>CCA2697548101MSH2c.367-7T>C (n.367-7T>C)
c.169-7T>C (n.169-7T>C)
n.439-7T>C
n.429-7T>C
 ClinVar
2g.47410088delCA2573134692MSH2c.367-6del (n.367-6del)
c.169-6del (n.169-6del)
n.439-6del
n.429-6del
 ClinVar dbSNP gnomAD v4
2g.47410088A=CA2495831108MSH2c.367-6A= (n.367-6A=)
c.169-6A= (n.169-6A=)
n.439-6A=
n.429-6A=
2g.47410088A>GCA038274MSH2c.367-6A>G (n.367-6A>G)
c.169-6A>G (n.169-6A>G)
n.439-6A>G
n.429-6A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410088A>TCA038285MSH2c.367-6A>T (n.367-6A>T)
c.169-6A>T (n.169-6A>T)
n.439-6A>T
n.429-6A>T
 dbSNP ExAC gnomAD v2
2g.47410089C=CA2495831109MSH2c.367-5C= (n.367-5C=)
c.169-5C= (n.169-5C=)
n.439-5C=
n.429-5C=
2g.47410089C>GCA021072MSH2c.367-5C>G (n.367-5C>G)
c.169-5C>G (n.169-5C>G)
n.439-5C>G
n.429-5C>G
 ClinVar dbSNP gnomAD v4
2g.47410089C>TCA021075MSH2c.367-5C>T (n.367-5C>T)
c.169-5C>T (n.169-5C>T)
n.439-5C>T
n.429-5C>T
 ClinVar dbSNP gnomAD v4
2g.47410090T>CCA915943882MSH2c.367-4T>C (n.367-4T>C)
c.169-4T>C (n.169-4T>C)
n.439-4T>C
n.429-4T>C
 ClinVar dbSNP gnomAD v4
2g.47410090T>GCA10577934MSH2c.367-4T>G (n.367-4T>G)
c.169-4T>G (n.169-4T>G)
n.439-4T>G
n.429-4T>G
 ClinVar dbSNP
2g.47410090T=CA2495831110MSH2c.367-4T= (n.367-4T=)
c.169-4T= (n.169-4T=)
n.439-4T=
n.429-4T=
2g.47410091delCA2580067486MSH2c.367-3del (n.367-3del)
c.169-3del (n.169-3del)
n.439-3del
n.429-3del
 ClinVar
2g.47410092_47411114delCA2499216005MSH2c.367-2_645+742del
c.169-2_447+742del
n.439-2_717+742del
n.429-2_707+742del
 ClinVar
2g.47410091T>ACA2695200733MSH2c.367-3T>A (n.367-3T>A)
c.169-3T>A (n.169-3T>A)
n.439-3T>A
n.429-3T>A
 ClinVar
2g.47410091T>CCA913187946MSH2c.367-3T>C (n.367-3T>C)
c.169-3T>C (n.169-3T>C)
n.439-3T>C
n.429-3T>C
 ClinVar dbSNP
2g.47410091T>GCA891842929MSH2c.367-3T>G (n.367-3T>G)
c.169-3T>G (n.169-3T>G)
n.439-3T>G
n.429-3T>G
 ClinVar dbSNP
2g.47410091T=CA2495831111MSH2c.367-3T= (n.367-3T=)
c.169-3T= (n.169-3T=)
n.439-3T=
n.429-3T=
2g.47410092_47410804delCA2499216007MSH2c.367-2_645+432del
c.169-2_447+432del
n.439-2_717+432del
n.429-2_707+432del
 ClinVar dbSNP
2g.47410091_47411003delCA2499216006MSH2c.367-3_645+631del
c.169-3_447+631del
n.439-3_717+631del
n.429-3_707+631del
 ClinVar dbSNP
2g.47410092A>CCA346730328MSH2c.367-2A>C (n.367-2A>C)
c.169-2A>C (n.169-2A>C)
n.439-2A>C
n.429-2A>C
2g.47410092A>GCA346730329MSH2c.367-2A>G (n.367-2A>G)
c.169-2A>G (n.169-2A>G)
n.439-2A>G
n.429-2A>G
 ClinVar
2g.47410092A>TCA346730330MSH2c.367-2A>T (n.367-2A>T)
c.169-2A>T (n.169-2A>T)
n.439-2A>T
n.429-2A>T
 dbSNP
2g.47410092_47410093delinsAGCA2495831112MSH2c.367-2_367-1delinsAG (n.367-2_367-1delinsAG)
c.169-2_169-1delinsAG (n.169-2_169-1delinsAG)
n.439-2_439-1delinsAG
n.429-2_429-1delinsAG
2g.47410092_47410373delCA2499216008MSH2c.367-2_645+1del
c.169-2_447+1del
n.439-2_717+1del
n.429-2_707+1del
 ClinVar dbSNP
2g.47410095_47410373delCA2581463443MSH2c.368_645+1del
c.170_447+1del
n.440_717+1del
n.430_707+1del
2g.47410093G>ACA021069MSH2c.367-1G>A (n.367-1G>A)
c.169-1G>A (n.169-1G>A)
n.439-1G>A
n.429-1G>A
 ClinVar dbSNP
2g.47410093G>CCA346730331MSH2c.367-1G>C (n.367-1G>C)
c.169-1G>C (n.169-1G>C)
n.439-1G>C
n.429-1G>C
 ClinVar dbSNP
2g.47410093G=CA2495831113MSH2c.367-1G= (n.367-1G=)
c.169-1G= (n.169-1G=)
n.439-1G=
n.429-1G=
2g.47410093G>TCA038168MSH2c.367-1G>T (n.367-1G>T)
c.169-1G>T (n.169-1G>T)
n.439-1G>T
n.429-1G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410094dupCA2580067489MSH2c.367dup
c.169dup
n.439dup
n.429dup
 ClinVar
2g.47410094delCA1139656940MSH2c.367del
c.169del
n.439del
n.429del
 ClinVar dbSNP
2g.47410093_47410097delCA2739274402MSH2c.367-1_370del
c.169-1_172del
n.439-1_442del
n.429-1_432del
 ClinVar
2g.47410094G>ACA038305MSH2c.367G>A (p.Ala123Thr)
c.169G>A (p.Ala57Thr)
n.439G>A
n.429G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410094G>CCA346730332MSH2c.367G>C (p.Ala123Pro)
c.169G>C (p.Ala57Pro)
n.439G>C
n.429G>C
 dbSNP
2g.47410094G=CA2495831114MSH2c.367G= (p.Ala123=)
c.169G= (p.Ala57=)
n.439G=
n.429G=
2g.47410094G>TCA346730333MSH2c.367G>T (p.Ala123Ser)
c.169G>T (p.Ala57Ser)
n.439G>T
n.429G>T
 ClinVar dbSNP
2g.47410094_47410095delinsGCCA2495831115MSH2c.367_368delinsGC (p.Ala123=)
c.169_170delinsGC (p.Ala57=)
n.439_440delinsGC
n.429_430delinsGC
2g.47410095delCA021083MSH2c.368del (p.Ala123ValfsTer?)
c.170del (p.Ala57ValfsTer?)
n.440del
n.430del
 ClinVar dbSNP
2g.47410095C>ACA346730334MSH2c.368C>A (p.Ala123Asp)
c.170C>A (p.Ala57Asp)
n.440C>A
n.430C>A
 dbSNP
2g.47410095C=CA2495831116MSH2c.368C= (p.Ala123=)
c.170C= (p.Ala57=)
n.440C=
n.430C=
2g.47410095C>GCA021080MSH2c.368C>G (p.Ala123Gly)
c.170C>G (p.Ala57Gly)
n.440C>G
n.430C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47410095C>TCA038326MSH2c.368C>T (p.Ala123Val)
c.170C>T (p.Ala57Val)
n.440C>T
n.430C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410096T>ACA426119403MSH2c.369T>A (p.Ala123=)
c.171T>A (p.Ala57=)
n.441T>A
n.431T>A
 dbSNP
2g.47410096T>CCA426119402MSH2c.369T>C (p.Ala123=)
c.171T>C (p.Ala57=)
n.441T>C
n.431T>C
 ClinVar
2g.47410096T>GCA426119401MSH2c.369T>G (p.Ala123=)
c.171T>G (p.Ala57=)
n.441T>G
n.431T>G
 ClinVar
2g.47410097delCA2580067492MSH2c.370del (p.Ser124LeufsTer?)
c.172del (p.Ser58LeufsTer?)
n.442del
n.432del
 ClinVar
2g.47410097T>ACA346730335MSH2c.370T>A (p.Ser124Thr)
c.172T>A (p.Ser58Thr)
n.442T>A
n.432T>A
 ClinVar dbSNP
2g.47410097T>CCA346730336MSH2c.370T>C (p.Ser124Pro)
c.172T>C (p.Ser58Pro)
n.442T>C
n.432T>C
 dbSNP
2g.47410097T>GCA346730337MSH2c.370T>G (p.Ser124Ala)
c.172T>G (p.Ser58Ala)
n.442T>G
n.432T>G
2g.47410098C>ACA346730338MSH2c.371C>A (p.Ser124Tyr)
c.173C>A (p.Ser58Tyr)
n.443C>A
n.433C>A
 dbSNP
2g.47410098C=CA2495831117MSH2c.371C= (p.Ser124=)
c.173C= (p.Ser58=)
n.443C=
n.433C=
2g.47410098C>GCA346730339MSH2c.371C>G (p.Ser124Cys)
c.173C>G (p.Ser58Cys)
n.443C>G
n.433C>G
 ClinVar dbSNP
2g.47410098C>TCA346730340MSH2c.371C>T (p.Ser124Phe)
c.173C>T (p.Ser58Phe)
n.443C>T
n.433C>T
 ClinVar dbSNP gnomAD v4
2g.47410100_47410102delCA2573134693MSH2c.373_375del (p.Pro125del)
c.175_177del (p.Pro59del)
n.445_447del
n.435_437del
 ClinVar dbSNP
2g.47410099T>ACA426119406MSH2c.372T>A (p.Ser124=)
c.174T>A (p.Ser58=)
n.444T>A
n.434T>A
2g.47410099T>CCA426119407MSH2c.372T>C (p.Ser124=)
c.174T>C (p.Ser58=)
n.444T>C
n.434T>C
 gnomAD v4
2g.47410099T>GCA426119408MSH2c.372T>G (p.Ser124=)
c.174T>G (p.Ser58=)
n.444T>G
n.434T>G
2g.47410100C>ACA346730341MSH2c.373C>A (p.Pro125Thr)
c.175C>A (p.Pro59Thr)
n.445C>A
n.435C>A
 ClinVar dbSNP
2g.47410100C=CA2495831118MSH2c.373C= (p.Pro125=)
c.175C= (p.Pro59=)
n.445C=
n.435C=
2g.47410100C>GCA346730342MSH2c.373C>G (p.Pro125Ala)
c.175C>G (p.Pro59Ala)
n.445C>G
n.435C>G
 ClinVar dbSNP
2g.47410100C>TCA038365MSH2c.373C>T (p.Pro125Ser)
c.175C>T (p.Pro59Ser)
n.445C>T
n.435C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410101delCA2580067495MSH2c.374del (p.Pro125LeufsTer?)
c.176del (p.Pro59LeufsTer?)
n.446del
n.436del
 ClinVar
2g.47410101C>ACA346730343MSH2c.374C>A (p.Pro125His)
c.176C>A (p.Pro59His)
n.446C>A
n.436C>A
 gnomAD v4
2g.47410101C=CA2495831119MSH2c.374C= (p.Pro125=)
c.176C= (p.Pro59=)
n.446C=
n.436C=
2g.47410101C>GCA346730344MSH2c.374C>G (p.Pro125Arg)
c.176C>G (p.Pro59Arg)
n.446C>G
n.436C>G
 ClinVar dbSNP
2g.47410101C>TCA10577935MSH2c.374C>T (p.Pro125Leu)
c.176C>T (p.Pro59Leu)
n.446C>T
n.436C>T
 ClinVar dbSNP gnomAD v4
2g.47410102T>ACA426119410MSH2c.375T>A (p.Pro125=)
c.177T>A (p.Pro59=)
n.447T>A
n.437T>A
2g.47410102T>CCA426119411MSH2c.375T>C (p.Pro125=)
c.177T>C (p.Pro59=)
n.447T>C
n.437T>C
2g.47410102T>GCA426119412MSH2c.375T>G (p.Pro125=)
c.177T>G (p.Pro59=)
n.447T>G
n.437T>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410102T=CA2495831120MSH2c.375T= (p.Pro125=)
c.177T= (p.Pro59=)
n.447T=
n.437T=
2g.47410103G>ACA021086MSH2c.376G>A (p.Gly126Ser)
c.178G>A (p.Gly60Ser)
n.448G>A
n.438G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410103G>CCA16042055MSH2c.376G>C (p.Gly126Arg)
c.178G>C (p.Gly60Arg)
n.448G>C
n.438G>C
 ClinVar dbSNP
2g.47410103G=CA2495831121MSH2c.376G= (p.Gly126=)
c.178G= (p.Gly60=)
n.448G=
n.438G=
2g.47410103G>TCA346730345MSH2c.376G>T (p.Gly126Cys)
c.178G>T (p.Gly60Cys)
n.448G>T
n.438G>T
 dbSNP
2g.47410104delCA2499216009MSH2c.377del (p.Gly126AlafsTer?)
c.179del (p.Gly60AlafsTer?)
n.449del
n.439del
 ClinVar dbSNP
2g.47410103_47410112delinsCACA2580067497MSH2c.376_385delinsCA (p.Gly126HisfsTer4)
c.178_187delinsCA (p.Gly60HisfsTer4)
n.448_457delinsCA
n.438_447delinsCA
 ClinVar
2g.47410104G>ACA346730346MSH2c.377G>A (p.Gly126Asp)
c.179G>A (p.Gly60Asp)
n.449G>A
n.439G>A
 ClinVar dbSNP
2g.47410104G>CCA346730347MSH2c.377G>C (p.Gly126Ala)
c.179G>C (p.Gly60Ala)
n.449G>C
n.439G>C
 dbSNP
2g.47410104G=CA2495831122MSH2c.377G= (p.Gly126=)
c.179G= (p.Gly60=)
n.449G=
n.439G=
2g.47410104G>TCA346730348MSH2c.377G>T (p.Gly126Val)
c.179G>T (p.Gly60Val)
n.449G>T
n.439G>T
 ClinVar dbSNP
2g.47410105C>ACA426119413MSH2c.378C>A (p.Gly126=)
c.180C>A (p.Gly60=)
n.450C>A
n.440C>A
 dbSNP
2g.47410105C=CA2495831123MSH2c.378C= (p.Gly126=)
c.180C= (p.Gly60=)
n.450C=
n.440C=
2g.47410105C>GCA426119415MSH2c.378C>G (p.Gly126=)
c.180C>G (p.Gly60=)
n.450C>G
n.440C>G
 dbSNP
2g.47410105C>TCA426119416MSH2c.378C>T (p.Gly126=)
c.180C>T (p.Gly60=)
n.450C>T
n.440C>T
 dbSNP
2g.47410106A>CCA346730349MSH2c.379A>C (p.Asn127His)
c.181A>C (p.Asn61His)
n.451A>C
n.441A>C
2g.47410106A>GCA346730350MSH2c.379A>G (p.Asn127Asp)
c.181A>G (p.Asn61Asp)
n.451A>G
n.441A>G
 ClinVar gnomAD v4
2g.47410106A>TCA346730351MSH2c.379A>T (p.Asn127Tyr)
c.181A>T (p.Asn61Tyr)
n.451A>T
n.441A>T
 ClinVar dbSNP
2g.47410106_47410107delCA2580067502MSH2c.379_380del (p.Asn127SerfsTer5)
c.181_182del (p.Asn61SerfsTer5)
n.451_452del
n.441_442del
 ClinVar
2g.47410107dupCA913189517MSH2c.380dup (p.Asn127LysfsTer6)
c.182dup (p.Asn61LysfsTer6)
n.452dup
n.442dup
 ClinVar dbSNP
2g.47410107delCA2580067501MSH2c.380del (p.Asn127IlefsTer?)
c.182del (p.Asn61IlefsTer?)
n.452del
n.442del
 ClinVar
2g.47410106_47410108delinsAATCA2495831124MSH2c.379_381delinsAAT (p.Asn127=)
c.181_183delinsAAT (p.Asn61=)
n.451_453delinsAAT
n.441_443delinsAAT
2g.47410107A=CA2495831126MSH2c.380A= (p.Asn127=)
c.182A= (p.Asn61=)
n.452A=
n.442A=
2g.47410107A>CCA346730352MSH2c.380A>C (p.Asn127Thr)
c.182A>C (p.Asn61Thr)
n.452A>C
n.442A>C
 ClinVar dbSNP
2g.47410107A>GCA021092MSH2c.380A>G (p.Asn127Ser)
c.182A>G (p.Asn61Ser)
n.452A>G
n.442A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410107A>TCA021096MSH2c.380A>T (p.Asn127Ile)
c.182A>T (p.Asn61Ile)
n.452A>T
n.442A>T
 dbSNP
2g.47410107_47410108delCA021090MSH2c.380_381del (p.Asn127ThrfsTer5)
c.182_183del (p.Asn61ThrfsTer5)
n.452_453del
n.442_443del
 ClinVar dbSNP
2g.47410107_47410109delinsATCCA2495831125MSH2c.380_382delinsATC (p.Asn127=)
c.182_184delinsATC (p.Asn61=)
n.452_454delinsATC
n.442_444delinsATC
2g.47410108T>ACA346730353MSH2c.381T>A (p.Asn127Lys)
c.183T>A (p.Asn61Lys)
n.453T>A
n.443T>A
 dbSNP
2g.47410108T>CCA426119418MSH2c.381T>C (p.Asn127=)
c.183T>C (p.Asn61=)
n.453T>C
n.443T>C
 ClinVar dbSNP
2g.47410108T>GCA346730354MSH2c.381T>G (p.Asn127Lys)
c.183T>G (p.Asn61Lys)
n.453T>G
n.443T>G
 dbSNP
2g.47410114_47410115delCA021112MSH2c.387_388del (p.Gln130ValfsTer2)
c.189_190del (p.Gln64ValfsTer2)
n.459_460del
n.449_450del
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410112_47410115delCA658760498MSH2c.385_388del (p.Gln130LeufsTer?)
c.187_190del (p.Gln64LeufsTer?)
n.457_460del
n.447_450del
 ClinVar
2g.47410109C>ACA346730355MSH2c.382C>A (p.Leu128Ile)
c.184C>A (p.Leu62Ile)
n.454C>A
n.444C>A
 dbSNP gnomAD v4
2g.47410109C=CA2495831127MSH2c.382C= (p.Leu128=)
c.184C= (p.Leu62=)
n.454C=
n.444C=
2g.47410109C>GCA021100MSH2c.382C>G (p.Leu128Val)
c.184C>G (p.Leu62Val)
n.454C>G
n.444C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410109C>TCA346730356MSH2c.382C>T (p.Leu128Phe)
c.184C>T (p.Leu62Phe)
n.454C>T
n.444C>T
 dbSNP
2g.47410110T>ACA346730357MSH2c.383T>A (p.Leu128His)
c.185T>A (p.Leu62His)
n.455T>A
n.445T>A
 dbSNP
2g.47410110T>CCA346730358MSH2c.383T>C (p.Leu128Pro)
c.185T>C (p.Leu62Pro)
n.455T>C
n.445T>C
 ClinVar
2g.47410110T>GCA021103MSH2c.383T>G (p.Leu128Arg)
c.185T>G (p.Leu62Arg)
n.455T>G
n.445T>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47410110T=CA2495831128MSH2c.383T= (p.Leu128=)
c.185T= (p.Leu62=)
n.455T=
n.445T=
2g.47410111C>ACA10577936MSH2c.384C>A (p.Leu128=)
c.186C>A (p.Leu62=)
n.456C>A
n.446C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410111C=CA2495831129MSH2c.384C= (p.Leu128=)
c.186C= (p.Leu62=)
n.456C=
n.446C=
2g.47410111C>GCA038413MSH2c.384C>G (p.Leu128=)
c.186C>G (p.Leu62=)
n.456C>G
n.446C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410111C>TCA426119419MSH2c.384C>T (p.Leu128=)
c.186C>T (p.Leu62=)
n.456C>T
n.446C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47410112T>ACA346730361MSH2c.385T>A (p.Ser129Thr)
c.187T>A (p.Ser63Thr)
n.457T>A
n.447T>A
 dbSNP
2g.47410112T>CCA346730359MSH2c.385T>C (p.Ser129Pro)
c.187T>C (p.Ser63Pro)
n.457T>C
n.447T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47410112T>GCA346730360MSH2c.385T>G (p.Ser129Ala)
c.187T>G (p.Ser63Ala)
n.457T>G
n.447T>G
2g.47410112T=CA2495831130MSH2c.385T= (p.Ser129=)
c.187T= (p.Ser63=)
n.457T=
n.447T=
2g.47410113C>ACA346730362MSH2c.386C>A (p.Ser129Tyr)
c.188C>A (p.Ser63Tyr)
n.458C>A
n.448C>A
2g.47410113C=CA2495831131MSH2c.386C= (p.Ser129=)
c.188C= (p.Ser63=)
n.458C=
n.448C=
2g.47410113C>GCA021106MSH2c.386C>G (p.Ser129Cys)
c.188C>G (p.Ser63Cys)
n.458C>G
n.448C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410113C>TCA021109MSH2c.386C>T (p.Ser129Phe)
c.188C>T (p.Ser63Phe)
n.458C>T
n.448C>T
 ClinVar dbSNP ExAC gnomAD v2
2g.47410114T>ACA426119427MSH2c.387T>A (p.Ser129=)
c.189T>A (p.Ser63=)
n.459T>A
n.449T>A
2g.47410114T>CCA426119423MSH2c.387T>C (p.Ser129=)
c.189T>C (p.Ser63=)
n.459T>C
n.449T>C
2g.47410114T>GCA426119425MSH2c.387T>G (p.Ser129=)
c.189T>G (p.Ser63=)
n.459T>G
n.449T>G
2g.47410114_47410116delinsTCACA2495831132MSH2c.387_389delinsTCA (p.Ser129=)
c.189_191delinsTCA (p.Ser63=)
n.459_461delinsTCA
n.449_451delinsTCA
2g.47410115C>ACA346730364MSH2c.388C>A (p.Gln130Lys)
c.190C>A (p.Gln64Lys)
n.460C>A
n.450C>A
2g.47410115C=CA2495831133MSH2c.388C= (p.Gln130=)
c.190C= (p.Gln64=)
n.460C=
n.450C=
2g.47410115C>GCA346730363MSH2c.388C>G (p.Gln130Glu)
c.190C>G (p.Gln64Glu)
n.460C>G
n.450C>G
 ClinVar dbSNP
2g.47410115C>TCA16610998MSH2c.388C>T (p.Gln130Ter)
c.190C>T (p.Gln64Ter)
n.460C>T
n.450C>T
 ClinVar dbSNP
2g.47410115_47410116delCA021115MSH2c.388_389del (p.Gln130ValfsTer2)
c.190_191del (p.Gln64ValfsTer2)
n.460_461del
n.450_451del
 ClinVar dbSNP gnomAD v4
2g.47410116A>CCA346730365MSH2c.389A>C (p.Gln130Pro)
c.191A>C (p.Gln64Pro)
n.461A>C
n.451A>C
2g.47410116A>GCA346730366MSH2c.389A>G (p.Gln130Arg)
c.191A>G (p.Gln64Arg)
n.461A>G
n.451A>G
2g.47410116A>TCA346730367MSH2c.389A>T (p.Gln130Leu)
c.191A>T (p.Gln64Leu)
n.461A>T
n.451A>T
 dbSNP
2g.47410117G>ACA426119428MSH2c.390G>A (p.Gln130=)
c.192G>A (p.Gln64=)
n.462G>A
n.452G>A
 dbSNP
2g.47410117G>CCA346730368MSH2c.390G>C (p.Gln130His)
c.192G>C (p.Gln64His)
n.462G>C
n.452G>C
 ClinVar dbSNP gnomAD v4
2g.47410117G=CA2495831134MSH2c.390G= (p.Gln130=)
c.192G= (p.Gln64=)
n.462G=
n.452G=
2g.47410117G>TCA346730369MSH2c.390G>T (p.Gln130His)
c.192G>T (p.Gln64His)
n.462G>T
n.452G>T
 ClinVar dbSNP
2g.47410118T>ACA346730370MSH2c.391T>A (p.Phe131Ile)
c.193T>A (p.Phe65Ile)
n.463T>A
n.453T>A
 dbSNP
2g.47410118T>CCA346730371MSH2c.391T>C (p.Phe131Leu)
c.193T>C (p.Phe65Leu)
n.463T>C
n.453T>C
 dbSNP
2g.47410118T>GCA038462MSH2c.391T>G (p.Phe131Val)
c.193T>G (p.Phe65Val)
n.463T>G
n.453T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410118T=CA2495831135MSH2c.391T= (p.Phe131=)
c.193T= (p.Phe65=)
n.463T=
n.453T=
2g.47410120_47410162dupCA2580067507MSH2c.393_435dup (p.Gly146Ter)
c.195_237dup (p.Gly80Ter)
n.465_507dup
n.455_497dup
 ClinVar
2g.47410119T>ACA346730372MSH2c.392T>A (p.Phe131Tyr)
c.194T>A (p.Phe65Tyr)
n.464T>A
n.454T>A
 dbSNP
2g.47410119T>CCA346730374MSH2c.392T>C (p.Phe131Ser)
c.194T>C (p.Phe65Ser)
n.464T>C
n.454T>C
 ClinVar
2g.47410119T>GCA346730373MSH2c.392T>G (p.Phe131Cys)
c.194T>G (p.Phe65Cys)
n.464T>G
n.454T>G
2g.47410120T>ACA346730375MSH2c.393T>A (p.Phe131Leu)
c.195T>A (p.Phe65Leu)
n.465T>A
n.455T>A
2g.47410120T>CCA426119430MSH2c.393T>C (p.Phe131=)
c.195T>C (p.Phe65=)
n.465T>C
n.455T>C
2g.47410120T>GCA346730376MSH2c.393T>G (p.Phe131Leu)
c.195T>G (p.Phe65Leu)
n.465T>G
n.455T>G
2g.47410121G>ACA346730377MSH2c.394G>A (p.Glu132Lys)
c.196G>A (p.Glu66Lys)
n.466G>A
n.456G>A
 dbSNP
2g.47410121G>CCA346730378MSH2c.394G>C (p.Glu132Gln)
c.196G>C (p.Glu66Gln)
n.466G>C
n.456G>C
 dbSNP
2g.47410121G>TCA346730379MSH2c.394G>T (p.Glu132Ter)
c.196G>T (p.Glu66Ter)
n.466G>T
n.456G>T
 ClinVar
2g.47410121dupCA2586969161MSH2c.394dup (p.Glu132GlyfsTer7)
c.196dup (p.Glu66GlyfsTer7)
n.466dup
n.456dup
2g.47410121_47410122insTTCA2580067642MSH2c.394_395insTT (p.Glu132ValfsTer?)
c.196_197insTT (p.Glu66ValfsTer?)
n.466_467insTT
n.456_457insTT
 ClinVar
2g.47410122A=CA2495831136MSH2c.395A= (p.Glu132=)
c.197A= (p.Glu66=)
n.467A=
n.457A=
2g.47410122A>CCA346730380MSH2c.395A>C (p.Glu132Ala)
c.197A>C (p.Glu66Ala)
n.467A>C
n.457A>C
2g.47410122A>GCA346730382MSH2c.395A>G (p.Glu132Gly)
c.197A>G (p.Glu66Gly)
n.467A>G
n.457A>G
2g.47410122A>TCA346730381MSH2c.395A>T (p.Glu132Val)
c.197A>T (p.Glu66Val)
n.467A>T
n.457A>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410123A>CCA346730383MSH2c.396A>C (p.Glu132Asp)
c.198A>C (p.Glu66Asp)
n.468A>C
n.458A>C
2g.47410123A>GCA426119432MSH2c.396A>G (p.Glu132=)
c.198A>G (p.Glu66=)
n.468A>G
n.458A>G
2g.47410123A>TCA346730384MSH2c.396A>T (p.Glu132Asp)
c.198A>T (p.Glu66Asp)
n.468A>T
n.458A>T
 dbSNP
2g.47410124G>ACA346730385MSH2c.397G>A (p.Asp133Asn)
c.199G>A (p.Asp67Asn)
n.469G>A
n.459G>A
 dbSNP
2g.47410124G>CCA346730386MSH2c.397G>C (p.Asp133His)
c.199G>C (p.Asp67His)
n.469G>C
n.459G>C
 dbSNP
2g.47410124G>TCA346730387MSH2c.397G>T (p.Asp133Tyr)
c.199G>T (p.Asp67Tyr)
n.469G>T
n.459G>T
 ClinVar dbSNP
2g.47410125A=CA2495831137MSH2c.398A= (p.Asp133=)
c.200A= (p.Asp67=)
n.470A=
n.460A=
2g.47410125A>CCA346730388MSH2c.398A>C (p.Asp133Ala)
c.200A>C (p.Asp67Ala)
n.470A>C
n.460A>C
 dbSNP
2g.47410125A>GCA46677666MSH2c.398A>G (p.Asp133Gly)
c.200A>G (p.Asp67Gly)
n.470A>G
n.460A>G
 ClinVar dbSNP
2g.47410125A>TCA346730389MSH2c.398A>T (p.Asp133Val)
c.200A>T (p.Asp67Val)
n.470A>T
n.460A>T
 dbSNP gnomAD v4
2g.47410125_47410126delinsACCA2495831138MSH2c.398_399delinsAC (p.Asp133=)
c.200_201delinsAC (p.Asp67=)
n.470_471delinsAC
n.460_461delinsAC
2g.47410126_47410127dupCA2586969162MSH2c.399_400dup (p.Ile134ThrfsTer?)
c.201_202dup (p.Ile68ThrfsTer?)
n.471_472dup
n.461_462dup
2g.47410126delCA021127MSH2c.399del (p.Asp133GlufsTer?)
c.201del (p.Asp67GlufsTer?)
n.471del
n.461del
 ClinVar dbSNP
2g.47410126C>ACA346730390MSH2c.399C>A (p.Asp133Glu)
c.201C>A (p.Asp67Glu)
n.471C>A
n.461C>A
2g.47410126C=CA2495831139MSH2c.399C= (p.Asp133=)
c.201C= (p.Asp67=)
n.471C=
n.461C=
2g.47410126C>GCA346730391MSH2c.399C>G (p.Asp133Glu)
c.201C>G (p.Asp67Glu)
n.471C>G
n.461C>G
 dbSNP
2g.47410126C>TCA021124MSH2c.399C>T (p.Asp133=)
c.201C>T (p.Asp67=)
n.471C>T
n.461C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410127A=CA2495831140MSH2c.400A= (p.Ile134=)
c.202A= (p.Ile68=)
n.472A=
n.462A=
2g.47410127A>CCA346730392MSH2c.400A>C (p.Ile134Leu)
c.202A>C (p.Ile68Leu)
n.472A>C
n.462A>C
 gnomAD v4
2g.47410127A>GCA346730394MSH2c.400A>G (p.Ile134Val)
c.202A>G (p.Ile68Val)
n.472A>G
n.462A>G
 ClinVar dbSNP gnomAD v4
2g.47410127A>TCA346730393MSH2c.400A>T (p.Ile134Phe)
c.202A>T (p.Ile68Phe)
n.472A>T
n.462A>T
 ClinVar dbSNP
2g.47410127_47410128delCA2580067643MSH2c.400_401del (p.Ile134SerfsTer4)
c.202_203del (p.Ile68SerfsTer4)
n.472_473del
n.462_463del
 ClinVar
2g.47410128T>ACA346730395MSH2c.401T>A (p.Ile134Asn)
c.203T>A (p.Ile68Asn)
n.473T>A
n.463T>A
2g.47410128T>CCA346730396MSH2c.401T>C (p.Ile134Thr)
c.203T>C (p.Ile68Thr)
n.473T>C
n.463T>C
 ClinVar gnomAD v4
2g.47410128T>GCA346730397MSH2c.401T>G (p.Ile134Ser)
c.203T>G (p.Ile68Ser)
n.473T>G
n.463T>G
2g.47410129T>ACA426119435MSH2c.402T>A (p.Ile134=)
c.204T>A (p.Ile68=)
n.474T>A
n.464T>A
 dbSNP
2g.47410129T>CCA426119434MSH2c.402T>C (p.Ile134=)
c.204T>C (p.Ile68=)
n.474T>C
n.464T>C
 dbSNP
2g.47410129T>GCA346730398MSH2c.402T>G (p.Ile134Met)
c.204T>G (p.Ile68Met)
n.474T>G
n.464T>G
2g.47410130C>ACA346730399MSH2c.403C>A (p.Leu135Ile)
c.205C>A (p.Leu69Ile)
n.475C>A
n.465C>A
 ClinVar dbSNP
2g.47410130C=CA2495831141MSH2c.403C= (p.Leu135=)
c.205C= (p.Leu69=)
n.475C=
n.465C=
2g.47410130C>GCA021133MSH2c.403C>G (p.Leu135Val)
c.205C>G (p.Leu69Val)
n.475C>G
n.465C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410130C>TCA021136MSH2c.403C>T (p.Leu135Phe)
c.205C>T (p.Leu69Phe)
n.475C>T
n.465C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410131T>ACA346730400MSH2c.404T>A (p.Leu135His)
c.206T>A (p.Leu69His)
n.476T>A
n.466T>A
 dbSNP
2g.47410131T>CCA346730401MSH2c.404T>C (p.Leu135Pro)
c.206T>C (p.Leu69Pro)
n.476T>C
n.466T>C
 dbSNP
2g.47410131T>GCA346730402MSH2c.404T>G (p.Leu135Arg)
c.206T>G (p.Leu69Arg)
n.476T>G
n.466T>G
2g.47410132C>ACA426119437MSH2c.405C>A (p.Leu135=)
c.207C>A (p.Leu69=)
n.477C>A
n.467C>A
2g.47410132C=CA2495831143MSH2c.405C= (p.Leu135=)
c.207C= (p.Leu69=)
n.477C=
n.467C=
2g.47410132C>GCA1649254MSH2c.405C>G (p.Leu135=)
c.207C>G (p.Leu69=)
n.477C>G
n.467C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.47410132C>TCA426119439MSH2c.405C>T (p.Leu135=)
c.207C>T (p.Leu69=)
n.477C>T
n.467C>T
 ClinVar dbSNP
2g.47410132_47410133delinsCTCA2495831142MSH2c.405_406delinsCT (p.Leu135=)
c.207_208delinsCT (p.Leu69=)
n.477_478delinsCT
n.467_468delinsCT
2g.47410133T>ACA346730405MSH2c.406T>A (p.Phe136Ile)
c.208T>A (p.Phe70Ile)
n.478T>A
n.468T>A
 dbSNP
2g.47410133T>CCA346730404MSH2c.406T>C (p.Phe136Leu)
c.208T>C (p.Phe70Leu)
n.478T>C
n.468T>C
 dbSNP gnomAD v4
2g.47410133T>GCA346730403MSH2c.406T>G (p.Phe136Val)
c.208T>G (p.Phe70Val)
n.478T>G
n.468T>G
2g.47410133T=CA2495831144MSH2c.406T= (p.Phe136=)
c.208T= (p.Phe70=)
n.478T=
n.468T=
2g.47410135delCA021138MSH2c.408del (p.Phe136LeufsTer?)
c.210del (p.Phe70LeufsTer?)
n.480del
n.470del
 ClinVar dbSNP ExAC
2g.47410134_47410135delCA2699074142MSH2c.407_408del (p.Phe136TrpfsTer2)
c.209_210del (p.Phe70TrpfsTer2)
n.479_480del
n.469_470del
 dbSNP
2g.47410134T>ACA346730406MSH2c.407T>A (p.Phe136Tyr)
c.209T>A (p.Phe70Tyr)
n.479T>A
n.469T>A
2g.47410134T>CCA346730407MSH2c.407T>C (p.Phe136Ser)
c.209T>C (p.Phe70Ser)
n.479T>C
n.469T>C
 ClinVar dbSNP
2g.47410134T>GCA346730408MSH2c.407T>G (p.Phe136Cys)
c.209T>G (p.Phe70Cys)
n.479T>G
n.469T>G
 gnomAD v4
2g.47410135T>ACA346730409MSH2c.408T>A (p.Phe136Leu)
c.210T>A (p.Phe70Leu)
n.480T>A
n.470T>A
2g.47410135T>CCA426119441MSH2c.408T>C (p.Phe136=)
c.210T>C (p.Phe70=)
n.480T>C
n.470T>C
 ClinVar dbSNP gnomAD v4
2g.47410135T>GCA346730410MSH2c.408T>G (p.Phe136Leu)
c.210T>G (p.Phe70Leu)
n.480T>G
n.470T>G
 ClinVar dbSNP
2g.47410135T=CA2495831145MSH2c.408T= (p.Phe136=)
c.210T= (p.Phe70=)
n.480T=
n.470T=
2g.47410136G>ACA346730411MSH2c.409G>A (p.Gly137Ser)
c.211G>A (p.Gly71Ser)
n.481G>A
n.471G>A
 dbSNP
2g.47410136G>CCA021142MSH2c.409G>C (p.Gly137Arg)
c.211G>C (p.Gly71Arg)
n.481G>C
n.471G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410136G=CA2495831146MSH2c.409G= (p.Gly137=)
c.211G= (p.Gly71=)
n.481G=
n.471G=
2g.47410136G>TCA346730412MSH2c.409G>T (p.Gly137Cys)
c.211G>T (p.Gly71Cys)
n.481G>T
n.471G>T
 dbSNP COSMIC
2g.47410137G>ACA346730413MSH2c.410G>A (p.Gly137Asp)
c.212G>A (p.Gly71Asp)
n.482G>A
n.472G>A
 dbSNP
2g.47410137G>CCA346730414MSH2c.410G>C (p.Gly137Ala)
c.212G>C (p.Gly71Ala)
n.482G>C
n.472G>C
 ClinVar dbSNP
2g.47410137G=CA2495831147MSH2c.410G= (p.Gly137=)
c.212G= (p.Gly71=)
n.482G=
n.472G=
2g.47410137G>TCA346730415MSH2c.410G>T (p.Gly137Val)
c.212G>T (p.Gly71Val)
n.482G>T
n.472G>T
 ClinVar dbSNP
2g.47410138T>ACA426119443MSH2c.411T>A (p.Gly137=)
c.213T>A (p.Gly71=)
n.483T>A
n.473T>A
2g.47410138T>CCA426119444MSH2c.411T>C (p.Gly137=)
c.213T>C (p.Gly71=)
n.483T>C
n.473T>C
2g.47410138T>GCA426119445MSH2c.411T>G (p.Gly137=)
c.213T>G (p.Gly71=)
n.483T>G
n.473T>G
2g.47410139A=CA2495831148MSH2c.412A= (p.Asn138=)
c.214A= (p.Asn72=)
n.484A=
n.474A=
2g.47410139A>CCA346730416MSH2c.412A>C (p.Asn138His)
c.214A>C (p.Asn72His)
n.484A>C
n.474A>C
2g.47410139A>GCA346730418MSH2c.412A>G (p.Asn138Asp)
c.214A>G (p.Asn72Asp)
n.484A>G
n.474A>G
 ClinVar dbSNP gnomAD v4
2g.47410139A>TCA346730417MSH2c.412A>T (p.Asn138Tyr)
c.214A>T (p.Asn72Tyr)
n.484A>T
n.474A>T
 ClinVar dbSNP
2g.47410140dupCA2695200734MSH2c.413dup (p.Asn138LysfsTer3)
c.215dup (p.Asn72LysfsTer3)
n.485dup
n.475dup
 ClinVar
2g.47410140delCA2699275583MSH2c.413del (p.Asn138ThrfsTer?)
c.215del (p.Asn72ThrfsTer?)
n.485del
n.475del
 dbSNP
2g.47410140A=CA2495831149MSH2c.413A= (p.Asn138=)
c.215A= (p.Asn72=)
n.485A=
n.475A=
2g.47410140A>CCA346730419MSH2c.413A>C (p.Asn138Thr)
c.215A>C (p.Asn72Thr)
n.485A>C
n.475A>C
2g.47410140A>GCA038614MSH2c.413A>G (p.Asn138Ser)
c.215A>G (p.Asn72Ser)
n.485A>G
n.475A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410140A>TCA346730420MSH2c.413A>T (p.Asn138Ile)
c.215A>T (p.Asn72Ile)
n.485A>T
n.475A>T
 dbSNP gnomAD v4
2g.47410141C>ACA346730421MSH2c.414C>A (p.Asn138Lys)
c.216C>A (p.Asn72Lys)
n.486C>A
n.476C>A
 ClinVar dbSNP
2g.47410141C=CA2495831151MSH2c.414C= (p.Asn138=)
c.216C= (p.Asn72=)
n.486C=
n.476C=
2g.47410141C>GCA346730422MSH2c.414C>G (p.Asn138Lys)
c.216C>G (p.Asn72Lys)
n.486C>G
n.476C>G
 ClinVar dbSNP
2g.47410141C>TCA426119446MSH2c.414C>T (p.Asn138=)
c.216C>T (p.Asn72=)
n.486C>T
n.476C>T
 dbSNP
2g.47410141_47410142delinsCACA2495831150MSH2c.414_415delinsCA (p.Asn138=)
c.216_217delinsCA (p.Asn72=)
n.486_487delinsCA
n.476_477delinsCA
2g.47410141_47410144delinsCAATCA2495831152MSH2c.414_417delinsCAAT (p.Asn138=)
c.216_219delinsCAAT (p.Asn72=)
n.486_489delinsCAAT
n.476_479delinsCAAT
2g.47410142A=CA2495831153MSH2c.415A= (p.Asn139=)
c.217A= (p.Asn73=)
n.487A=
n.477A=
2g.47410142A>CCA346730423MSH2c.415A>C (p.Asn139His)
c.217A>C (p.Asn73His)
n.487A>C
n.477A>C
2g.47410142A>GCA346730424MSH2c.415A>G (p.Asn139Asp)
c.217A>G (p.Asn73Asp)
n.487A>G
n.477A>G
 ClinVar dbSNP
2g.47410142A>TCA346730425MSH2c.415A>T (p.Asn139Tyr)
c.217A>T (p.Asn73Tyr)
n.487A>T
n.477A>T
2g.47410143delCA021145MSH2c.416del (p.Asn139MetfsTer?)
c.218del (p.Asn73MetfsTer?)
n.488del
n.478del
 ClinVar dbSNP
2g.47410142_47410144delCA1139656942MSH2c.415_417del (p.Asn139del)
c.217_219del (p.Asn73del)
n.487_489del
n.477_479del
 ClinVar dbSNP
2g.47410143A=CA2495831154MSH2c.416A= (p.Asn139=)
c.218A= (p.Asn73=)
n.488A=
n.478A=
2g.47410143A>CCA346730426MSH2c.416A>C (p.Asn139Thr)
c.218A>C (p.Asn73Thr)
n.488A>C
n.478A>C
2g.47410143A>GCA346730427MSH2c.416A>G (p.Asn139Ser)
c.218A>G (p.Asn73Ser)
n.488A>G
n.478A>G
 ClinVar dbSNP gnomAD v4
2g.47410143A>TCA346730428MSH2c.416A>T (p.Asn139Ile)
c.218A>T (p.Asn73Ile)
n.488A>T
n.478A>T
 dbSNP
2g.47410145_47410147delCA2586969163MSH2c.418_420del (p.Asp140del)
c.220_222del (p.Asp74del)
n.490_492del
n.480_482del
2g.47410144T>ACA346730429MSH2c.417T>A (p.Asn139Lys)
c.219T>A (p.Asn73Lys)
n.489T>A
n.479T>A
 dbSNP gnomAD v4
2g.47410144T>CCA426119450MSH2c.417T>C (p.Asn139=)
c.219T>C (p.Asn73=)
n.489T>C
n.479T>C
 ClinVar
2g.47410144T>GCA346730430MSH2c.417T>G (p.Asn139Lys)
c.219T>G (p.Asn73Lys)
n.489T>G
n.479T>G
2g.47410145G>ACA346730432MSH2c.418G>A (p.Asp140Asn)
c.220G>A (p.Asp74Asn)
n.490G>A
n.480G>A
 dbSNP
2g.47410145G>CCA346730431MSH2c.418G>C (p.Asp140His)
c.220G>C (p.Asp74His)
n.490G>C
n.480G>C
 dbSNP
2g.47410145G=CA2495831155MSH2c.418G= (p.Asp140=)
c.220G= (p.Asp74=)
n.490G=
n.480G=
2g.47410145G>TCA038631MSH2c.418G>T (p.Asp140Tyr)
c.220G>T (p.Asp74Tyr)
n.490G>T
n.480G>T
 dbSNP ExAC gnomAD v4
2g.47410145_47410147delinsGATCA2495831156MSH2c.418_420delinsGAT (p.Asp140=)
c.220_222delinsGAT (p.Asp74=)
n.490_492delinsGAT
n.480_482delinsGAT
2g.47410146A=CA2495831157MSH2c.419A= (p.Asp140=)
c.221A= (p.Asp74=)
n.491A=
n.481A=
2g.47410146A>CCA346730433MSH2c.419A>C (p.Asp140Ala)
c.221A>C (p.Asp74Ala)
n.491A>C
n.481A>C
 ClinVar dbSNP
2g.47410146A>GCA346730434MSH2c.419A>G (p.Asp140Gly)
c.221A>G (p.Asp74Gly)
n.491A>G
n.481A>G
 ClinVar dbSNP gnomAD v4
2g.47410146A>TCA346730435MSH2c.419A>T (p.Asp140Val)
c.221A>T (p.Asp74Val)
n.491A>T
n.481A>T
 ClinVar dbSNP
2g.47410148_47410149delCA337956MSH2c.421_422del (p.Met141ValfsTer10)
c.223_224del (p.Met75ValfsTer10)
n.493_494del
n.483_484del
 ClinVar dbSNP
2g.47410147T>ACA346730436MSH2c.420T>A (p.Asp140Glu)
c.222T>A (p.Asp74Glu)
n.492T>A
n.482T>A
 dbSNP
2g.47410147T>CCA426119456MSH2c.420T>C (p.Asp140=)
c.222T>C (p.Asp74=)
n.492T>C
n.482T>C
 gnomAD v4
2g.47410147T>GCA346730437MSH2c.420T>G (p.Asp140Glu)
c.222T>G (p.Asp74Glu)
n.492T>G
n.482T>G
2g.47410147_47410148insTTCA2580067647MSH2c.420_421insTT (p.Met141LeufsTer?)
c.222_223insTT (p.Met75LeufsTer?)
n.492_493insTT
n.482_483insTT
 ClinVar
2g.47410147dupCA645369180MSH2c.420dup (p.Met141TyrfsTer11)
c.222dup (p.Met75TyrfsTer11)
n.492dup
n.482dup
 ClinVar dbSNP
2g.47410148A=CA2495831158MSH2c.421A= (p.Met141=)
c.223A= (p.Met75=)
n.493A=
n.483A=
2g.47410148A>CCA346730438MSH2c.421A>C (p.Met141Leu)
c.223A>C (p.Met75Leu)
n.493A>C
n.483A>C
2g.47410148A>GCA021148MSH2c.421A>G (p.Met141Val)
c.223A>G (p.Met75Val)
n.493A>G
n.483A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410148A>TCA346730439MSH2c.421A>T (p.Met141Leu)
c.223A>T (p.Met75Leu)
n.493A>T
n.483A>T
 dbSNP
2g.47410149T>ACA346730441MSH2c.422T>A (p.Met141Lys)
c.224T>A (p.Met75Lys)
n.494T>A
n.484T>A
 dbSNP
2g.47410149T>CCA038657MSH2c.422T>C (p.Met141Thr)
c.224T>C (p.Met75Thr)
n.494T>C
n.484T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410149T>GCA346730440MSH2c.422T>G (p.Met141Arg)
c.224T>G (p.Met75Arg)
n.494T>G
n.484T>G
 gnomAD v4
2g.47410149T=CA2495831159MSH2c.422T= (p.Met141=)
c.224T= (p.Met75=)
n.494T=
n.484T=
2g.47410149_47410152dupCA2580067648MSH2c.422_425dup (p.Ala143ValfsTer10)
c.224_227dup (p.Ala77ValfsTer10)
n.494_497dup
n.484_487dup
 ClinVar
2g.47410150G>ACA346730442MSH2c.423G>A (p.Met141Ile)
c.225G>A (p.Met75Ile)
n.495G>A
n.485G>A
 ClinVar dbSNP
2g.47410150G>CCA346730443MSH2c.423G>C (p.Met141Ile)
c.225G>C (p.Met75Ile)
n.495G>C
n.485G>C
 dbSNP
2g.47410150G=CA2495831160MSH2c.423G= (p.Met141=)
c.225G= (p.Met75=)
n.495G=
n.485G=
2g.47410150G>TCA346730444MSH2c.423G>T (p.Met141Ile)
c.225G>T (p.Met75Ile)
n.495G>T
n.485G>T
2g.47410151T>ACA346730445MSH2c.424T>A (p.Ser142Thr)
c.226T>A (p.Ser76Thr)
n.496T>A
n.486T>A
 dbSNP
2g.47410151T>CCA346730446MSH2c.424T>C (p.Ser142Pro)
c.226T>C (p.Ser76Pro)
n.496T>C
n.486T>C
2g.47410151T>GCA16617557MSH2c.424T>G (p.Ser142Ala)
c.226T>G (p.Ser76Ala)
n.496T>G
n.486T>G
 ClinVar dbSNP gnomAD v4
2g.47410151T=CA2495831161MSH2c.424T= (p.Ser142=)
c.226T= (p.Ser76=)
n.496T=
n.486T=
2g.47410152_47410156dupCA2586969164MSH2c.425_429dup (p.Ser144GlnfsTer?)
c.227_231dup (p.Ser78GlnfsTer?)
n.497_501dup
n.487_491dup
2g.47410152C>ACA346730447MSH2c.425C>A (p.Ser142Ter)
c.227C>A (p.Ser76Ter)
n.497C>A
n.487C>A
 ClinVar dbSNP
2g.47410152C=CA2495831162MSH2c.425C= (p.Ser142=)
c.227C= (p.Ser76=)
n.497C=
n.487C=
2g.47410152C>GCA021151MSH2c.425C>G (p.Ser142Ter)
c.227C>G (p.Ser76Ter)
n.497C>G
n.487C>G
 ClinVar dbSNP
2g.47410152C>TCA346730448MSH2c.425C>T (p.Ser142Leu)
c.227C>T (p.Ser76Leu)
n.497C>T
n.487C>T
 ClinVar
2g.47410152dupCA2580067651MSH2c.425dup (p.Ala143SerfsTer9)
c.227dup (p.Ala77SerfsTer9)
n.497dup
n.487dup
 ClinVar
2g.47410153A=CA2495831163MSH2c.426A= (p.Ser142=)
c.228A= (p.Ser76=)
n.498A=
n.488A=
2g.47410153A>CCA426119459MSH2c.426A>C (p.Ser142=)
c.228A>C (p.Ser76=)
n.498A>C
n.488A>C
2g.47410153A>GCA46677721MSH2c.426A>G (p.Ser142=)
c.228A>G (p.Ser76=)
n.498A>G
n.488A>G
 ClinVar dbSNP gnomAD v4
2g.47410153A>TCA426119460MSH2c.426A>T (p.Ser142=)
c.228A>T (p.Ser76=)
n.498A>T
n.488A>T
 ClinVar dbSNP
2g.47410154G>ACA10581995MSH2c.427G>A (p.Ala143Thr)
c.229G>A (p.Ala77Thr)
n.499G>A
n.489G>A
 ClinVar dbSNP gnomAD v4
2g.47410154G>CCA346730449MSH2c.427G>C (p.Ala143Pro)
c.229G>C (p.Ala77Pro)
n.499G>C
n.489G>C
 dbSNP
2g.47410154G=CA2495831164MSH2c.427G= (p.Ala143=)
c.229G= (p.Ala77=)
n.499G=
n.489G=
2g.47410154G>TCA346730450MSH2c.427G>T (p.Ala143Ser)
c.229G>T (p.Ala77Ser)
n.499G>T
n.489G>T
 dbSNP gnomAD v2 gnomAD v4
2g.47410155C>ACA346730453MSH2c.428C>A (p.Ala143Asp)
c.230C>A (p.Ala77Asp)
n.500C>A
n.490C>A
 dbSNP
2g.47410155C=CA2495831166MSH2c.428C= (p.Ala143=)
c.230C= (p.Ala77=)
n.500C=
n.490C=
2g.47410155C>GCA346730451MSH2c.428C>G (p.Ala143Gly)
c.230C>G (p.Ala77Gly)
n.500C>G
n.490C>G
 ClinVar dbSNP gnomAD v4
2g.47410155C>TCA346730452MSH2c.428C>T (p.Ala143Val)
c.230C>T (p.Ala77Val)
n.500C>T
n.490C>T
 ClinVar dbSNP
2g.47410155_47410156delinsCTCA2495831165MSH2c.428_429delinsCT (p.Ala143=)
c.230_231delinsCT (p.Ala77=)
n.500_501delinsCT
n.490_491delinsCT
2g.47410156T>ACA426119464MSH2c.429T>A (p.Ala143=)
c.231T>A (p.Ala77=)
n.501T>A
n.491T>A
 dbSNP
2g.47410156T>CCA426119462MSH2c.429T>C (p.Ala143=)
c.231T>C (p.Ala77=)
n.501T>C
n.491T>C
 ClinVar dbSNP gnomAD v4
2g.47410156T>GCA426119461MSH2c.429T>G (p.Ala143=)
c.231T>G (p.Ala77=)
n.501T>G
n.491T>G
2g.47410156T=CA2495831167MSH2c.429T= (p.Ala143=)
c.231T= (p.Ala77=)
n.501T=
n.491T=
2g.47410157delCA1139656944MSH2c.430del (p.Ser144ProfsTer30)
c.232del (p.Ser78ProfsTer30)
n.502del
n.492del
 ClinVar dbSNP
2g.47410157T>ACA346730454MSH2c.430T>A (p.Ser144Thr)
c.232T>A (p.Ser78Thr)
n.502T>A
n.492T>A
2g.47410157T>CCA346730455MSH2c.430T>C (p.Ser144Pro)
c.232T>C (p.Ser78Pro)
n.502T>C
n.492T>C
 ClinVar gnomAD v4
2g.47410157T>GCA346730456MSH2c.430T>G (p.Ser144Ala)
c.232T>G (p.Ser78Ala)
n.502T>G
n.492T>G
 ClinVar dbSNP
2g.47410157T=CA2495831168MSH2c.430T= (p.Ser144=)
c.232T= (p.Ser78=)
n.502T=
n.492T=
2g.47410158C>ACA346730457MSH2c.431C>A (p.Ser144Tyr)
c.233C>A (p.Ser78Tyr)
n.503C>A
n.493C>A
2g.47410158C=CA2495831169MSH2c.431C= (p.Ser144=)
c.233C= (p.Ser78=)
n.503C=
n.493C=
2g.47410158C>GCA10581996MSH2c.431C>G (p.Ser144Cys)
c.233C>G (p.Ser78Cys)
n.503C>G
n.493C>G
 ClinVar dbSNP
2g.47410158C>TCA346730458MSH2c.431C>T (p.Ser144Phe)
c.233C>T (p.Ser78Phe)
n.503C>T
n.493C>T
2g.47410159delCA2586969165MSH2c.432del (p.Ile145LeufsTer29)
c.234del (p.Ile79LeufsTer29)
n.504del
n.494del
2g.47410159C>ACA426119466MSH2c.432C>A (p.Ser144=)
c.234C>A (p.Ser78=)
n.504C>A
n.494C>A
 dbSNP
2g.47410159C=CA2495831170MSH2c.432C= (p.Ser144=)
c.234C= (p.Ser78=)
n.504C=
n.494C=
2g.47410159C>GCA426119467MSH2c.432C>G (p.Ser144=)
c.234C>G (p.Ser78=)
n.504C>G
n.494C>G
 dbSNP
2g.47410159C>TCA426119468MSH2c.432C>T (p.Ser144=)
c.234C>T (p.Ser78=)
n.504C>T
n.494C>T
 ClinVar dbSNP gnomAD v4
2g.47410160A=CA2495831171MSH2c.433A= (p.Ile145=)
c.235A= (p.Ile79=)
n.505A=
n.495A=
2g.47410160A>CCA346730459MSH2c.433A>C (p.Ile145Leu)
c.235A>C (p.Ile79Leu)
n.505A>C
n.495A>C
2g.47410160A>GCA10577937MSH2c.433A>G (p.Ile145Val)
c.235A>G (p.Ile79Val)
n.505A>G
n.495A>G
 ClinVar dbSNP
2g.47410160A>TCA346730460MSH2c.433A>T (p.Ile145Phe)
c.235A>T (p.Ile79Phe)
n.505A>T
n.495A>T
2g.47410161T>ACA346730461MSH2c.434T>A (p.Ile145Asn)
c.236T>A (p.Ile79Asn)
n.506T>A
n.496T>A
2g.47410161T>CCA038704MSH2c.434T>C (p.Ile145Thr)
c.236T>C (p.Ile79Thr)
n.506T>C
n.496T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410161T>GCA346730462MSH2c.434T>G (p.Ile145Ser)
c.236T>G (p.Ile79Ser)
n.506T>G
n.496T>G
2g.47410161T=CA2495831172MSH2c.434T= (p.Ile145=)
c.236T= (p.Ile79=)
n.506T=
n.496T=
2g.47410162T>ACA426119471MSH2c.435T>A (p.Ile145=)
c.237T>A (p.Ile79=)
n.507T>A
n.497T>A
2g.47410162T>CCA426119472MSH2c.435T>C (p.Ile145=)
c.237T>C (p.Ile79=)
n.507T>C
n.497T>C
 ClinVar dbSNP
2g.47410162T>GCA021158MSH2c.435T>G (p.Ile145Met)
c.237T>G (p.Ile79Met)
n.507T>G
n.497T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410162T=CA2495831173MSH2c.435T= (p.Ile145=)
c.237T= (p.Ile79=)
n.507T=
n.497T=
2g.47410163G>ACA346730465MSH2c.436G>A (p.Gly146Ser)
c.238G>A (p.Gly80Ser)
n.508G>A
n.498G>A
 dbSNP gnomAD v4
2g.47410163G>CCA346730464MSH2c.436G>C (p.Gly146Arg)
c.238G>C (p.Gly80Arg)
n.508G>C
n.498G>C
 ClinVar dbSNP
2g.47410163G=CA2495831174MSH2c.436G= (p.Gly146=)
c.238G= (p.Gly80=)
n.508G=
n.498G=
2g.47410163G>TCA346730463MSH2c.436G>T (p.Gly146Cys)
c.238G>T (p.Gly80Cys)
n.508G>T
n.498G>T
 dbSNP
2g.47410164G>ACA346730467MSH2c.437G>A (p.Gly146Asp)
c.239G>A (p.Gly80Asp)
n.509G>A
n.499G>A
 dbSNP
2g.47410164G>CCA346730466MSH2c.437G>C (p.Gly146Ala)
c.239G>C (p.Gly80Ala)
n.509G>C
n.499G>C
 dbSNP
2g.47410164G=CA2495831175MSH2c.437G= (p.Gly146=)
c.239G= (p.Gly80=)
n.509G=
n.499G=
2g.47410164G>TCA021161MSH2c.437G>T (p.Gly146Val)
c.239G>T (p.Gly80Val)
n.509G>T
n.499G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410166_47410167dupCA891842930MSH2c.439_440dup (p.Val148LeufsTer27)
c.241_242dup (p.Val82LeufsTer27)
n.511_512dup
n.501_502dup
 ClinVar dbSNP
2g.47410167_47410171dupCA2580067655MSH2c.440_444dup (p.Gly149LeufsTer27)
c.242_246dup (p.Gly83LeufsTer27)
n.512_516dup
n.502_506dup
 ClinVar
2g.47410165T>ACA426119474MSH2c.438T>A (p.Gly146=)
c.240T>A (p.Gly80=)
n.510T>A
n.500T>A
2g.47410165T>CCA021164MSH2c.438T>C (p.Gly146=)
c.240T>C (p.Gly80=)
n.510T>C
n.500T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410165T>GCA021167MSH2c.438T>G (p.Gly146=)
c.240T>G (p.Gly80=)
n.510T>G
n.500T>G
 ClinVar dbSNP
2g.47410165T=CA2495831176MSH2c.438T= (p.Gly146=)
c.240T= (p.Gly80=)
n.510T=
n.500T=
2g.47410166G>ACA038750MSH2c.439G>A (p.Val147Ile)
c.241G>A (p.Val81Ile)
n.511G>A
n.501G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47410166G>CCA346730468MSH2c.439G>C (p.Val147Leu)
c.241G>C (p.Val81Leu)
n.511G>C
n.501G>C
 dbSNP
2g.47410166G=CA2495831177MSH2c.439G= (p.Val147=)
c.241G= (p.Val81=)
n.511G=
n.501G=
2g.47410166G>TCA346730469MSH2c.439G>T (p.Val147Phe)
c.241G>T (p.Val81Phe)
n.511G>T
n.501G>T
 dbSNP
2g.47410167T>ACA346730470MSH2c.440T>A (p.Val147Asp)
c.242T>A (p.Val81Asp)
n.512T>A
n.502T>A
 ClinVar dbSNP
2g.47410167T>CCA346730471MSH2c.440T>C (p.Val147Ala)
c.242T>C (p.Val81Ala)
n.512T>C
n.502T>C
2g.47410167T>GCA038774MSH2c.440T>G (p.Val147Gly)
c.242T>G (p.Val81Gly)
n.512T>G
n.502T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47410167T=CA2495831178MSH2c.440T= (p.Val147=)
c.242T= (p.Val81=)
n.512T=
n.502T=
2g.47410168delCA2580067657MSH2c.441del (p.Val148TrpfsTer26)
c.243del (p.Val82TrpfsTer26)
n.513del
n.503del
 ClinVar
2g.47410168T>ACA426119478MSH2c.441T>A (p.Val147=)
c.243T>A (p.Val81=)
n.513T>A
n.503T>A
2g.47410168T>CCA426119479MSH2c.441T>C (p.Val147=)
c.243T>C (p.Val81=)
n.513T>C
n.503T>C
2g.47410168T>GCA426119480MSH2c.441T>G (p.Val147=)
c.243T>G (p.Val81=)
n.513T>G
n.503T>G
 ClinVar
2g.47410169G>ACA346730472MSH2c.442G>A (p.Val148Met)
c.244G>A (p.Val82Met)
n.514G>A
n.504G>A
 ClinVar dbSNP
2g.47410169G>CCA346730473MSH2c.442G>C (p.Val148Leu)
c.244G>C (p.Val82Leu)
n.514G>C
n.504G>C
 ClinVar dbSNP gnomAD v4
2g.47410169G=CA2495831181MSH2c.442G= (p.Val148=)
c.244G= (p.Val82=)
n.514G=
n.504G=
2g.47410169G>TCA346730474MSH2c.442G>T (p.Val148Leu)
c.244G>T (p.Val82Leu)
n.514G>T
n.504G>T
2g.47410169_47410170delinsGTCA2495831180MSH2c.442_443delinsGT (p.Val148=)
c.244_245delinsGT (p.Val82=)
n.514_515delinsGT
n.504_505delinsGT
2g.47410172_47410175delCA2695200735MSH2c.445_448del (p.Gly149LeufsTer24)
c.247_250del (p.Gly83LeufsTer24)
n.517_520del
n.507_510del
 ClinVar dbSNP
2g.47410169_47410181delinsGTGGGTGTTAAAACA2495831179MSH2c.442_454delinsGTGGGTGTTAAAA (p.Val148=)
c.244_256delinsGTGGGTGTTAAAA (p.Val82=)
n.514_526delinsGTGGGTGTTAAAA
n.504_516delinsGTGGGTGTTAAAA
2g.47410170delCA658655685MSH2c.443del (p.Val148GlyfsTer26)
c.245del (p.Val82GlyfsTer26)
n.515del
n.505del
 ClinVar dbSNP
2g.47410170T>ACA346730475MSH2c.443T>A (p.Val148Glu)
c.245T>A (p.Val82Glu)
n.515T>A
n.505T>A
 ClinVar dbSNP
2g.47410170T>CCA346730476MSH2c.443T>C (p.Val148Ala)
c.245T>C (p.Val82Ala)
n.515T>C
n.505T>C
 ClinVar dbSNP
2g.47410170T>GCA346730477MSH2c.443T>G (p.Val148Gly)
c.245T>G (p.Val82Gly)
n.515T>G
n.505T>G
2g.47410170T=CA2495831182MSH2c.443T= (p.Val148=)
c.245T= (p.Val82=)
n.515T=
n.505T=
2g.47410172_47410183delCA645369181MSH2c.445_456del (p.Gly149_Met152del)
c.247_258del (p.Gly83_Met86del)
n.517_528del
n.507_518del
 ClinVar dbSNP
2g.47410171G>ACA426119481MSH2c.444G>A (p.Val148=)
c.246G>A (p.Val82=)
n.516G>A
n.506G>A
 dbSNP
2g.47410171G>CCA426119482MSH2c.444G>C (p.Val148=)
c.246G>C (p.Val82=)
n.516G>C
n.506G>C
 ClinVar dbSNP
2g.47410171G>TCA426119483MSH2c.444G>T (p.Val148=)
c.246G>T (p.Val82=)
n.516G>T
n.506G>T
 dbSNP gnomAD v4
2g.47410172G>ACA46677784MSH2c.445G>A (p.Gly149Ser)
c.247G>A (p.Gly83Ser)
n.517G>A
n.507G>A
 ClinVar dbSNP gnomAD v4
2g.47410172G>CCA346730478MSH2c.445G>C (p.Gly149Arg)
c.247G>C (p.Gly83Arg)
n.517G>C
n.507G>C
 ClinVar
2g.47410172G=CA2495831183MSH2c.445G= (p.Gly149=)
c.247G= (p.Gly83=)
n.517G=
n.507G=
2g.47410172G>TCA346730479MSH2c.445G>T (p.Gly149Cys)
c.247G>T (p.Gly83Cys)
n.517G>T
n.507G>T
2g.47410173G>ACA021170MSH2c.446G>A (p.Gly149Asp)
c.248G>A (p.Gly83Asp)
n.518G>A
n.508G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47410173G>CCA346730480MSH2c.446G>C (p.Gly149Ala)
c.248G>C (p.Gly83Ala)
n.518G>C
n.508G>C
 ClinVar dbSNP gnomAD v4
2g.47410173G=CA2495831184MSH2c.446G= (p.Gly149=)
c.248G= (p.Gly83=)
n.518G=
n.508G=
2g.47410173G>TCA346730481MSH2c.446G>T (p.Gly149Val)
c.248G>T (p.Gly83Val)
n.518G>T
n.508G>T
 ClinVar dbSNP gnomAD v4
2g.47410175_47410176delCA2695200736MSH2c.448_449del (p.Val150Ter)
c.250_251del (p.Val84Ter)
n.520_521del
n.510_511del
 ClinVar
2g.47410174T>ACA426119485MSH2c.447T>A (p.Gly149=)
c.249T>A (p.Gly83=)
n.519T>A
n.509T>A
 dbSNP
2g.47410174T>CCA021173MSH2c.447T>C (p.Gly149=)
c.249T>C (p.Gly83=)
n.519T>C
n.509T>C
 ClinVar dbSNP
2g.47410174T>GCA426119486MSH2c.447T>G (p.Gly149=)
c.249T>G (p.Gly83=)
n.519T>G
n.509T>G
 dbSNP
2g.47410174T=CA2495831185MSH2c.447T= (p.Gly149=)
c.249T= (p.Gly83=)
n.519T=
n.509T=
2g.47410175G>ACA346730482MSH2c.448G>A (p.Val150Ile)
c.250G>A (p.Val84Ile)
n.520G>A
n.510G>A
 ClinVar dbSNP gnomAD v4
2g.47410175G>CCA346730483MSH2c.448G>C (p.Val150Leu)
c.250G>C (p.Val84Leu)
n.520G>C
n.510G>C
 ClinVar dbSNP
2g.47410175G=CA2495831186MSH2c.448G= (p.Val150=)
c.250G= (p.Val84=)
n.520G=
n.510G=
2g.47410175G>TCA346730484MSH2c.448G>T (p.Val150Phe)
c.250G>T (p.Val84Phe)
n.520G>T
n.510G>T
 ClinVar dbSNP gnomAD v4 COSMIC
2g.47410175_47410179delCA2695200737MSH2c.448_452del (p.Val150AsnfsTer5)
c.250_254del (p.Val84AsnfsTer5)
n.520_524del
n.510_514del
 ClinVar
2g.47410176T>ACA346730485MSH2c.449T>A (p.Val150Asp)
c.251T>A (p.Val84Asp)
n.521T>A
n.511T>A
 dbSNP
2g.47410176T>CCA346730486MSH2c.449T>C (p.Val150Ala)
c.251T>C (p.Val84Ala)
n.521T>C
n.511T>C
 dbSNP gnomAD v4
2g.47410176T>GCA346730487MSH2c.449T>G (p.Val150Gly)
c.251T>G (p.Val84Gly)
n.521T>G
n.511T>G
 dbSNP gnomAD v4
2g.47410177delCA2695200738MSH2c.450del (p.Met152CysfsTer22)
c.252del (p.Met86CysfsTer22)
n.522del
n.512del
 ClinVar
2g.47410177T>ACA426119491MSH2c.450T>A (p.Val150=)
c.252T>A (p.Val84=)
n.522T>A
n.512T>A
2g.47410177T>CCA426119490MSH2c.450T>C (p.Val150=)
c.252T>C (p.Val84=)
n.522T>C
n.512T>C
2g.47410177T>GCA426119489MSH2c.450T>G (p.Val150=)
c.252T>G (p.Val84=)
n.522T>G
n.512T>G
2g.47410177_47410178delinsTACA2495831187MSH2c.450_451delinsTA (p.Val150=)
c.252_253delinsTA (p.Val84=)
n.522_523delinsTA
n.512_513delinsTA
2g.47410178A=CA2495831188MSH2c.451A= (p.Lys151=)
c.253A= (p.Lys85=)
n.523A=
n.513A=
2g.47410178A>CCA346730489MSH2c.451A>C (p.Lys151Gln)
c.253A>C (p.Lys85Gln)
n.523A>C
n.513A>C
2g.47410178A>GCA346730490MSH2c.451A>G (p.Lys151Glu)
c.253A>G (p.Lys85Glu)
n.523A>G
n.513A>G
 dbSNP
2g.47410178A>TCA346730488MSH2c.451A>T (p.Lys151Ter)
c.253A>T (p.Lys85Ter)
n.523A>T
n.513A>T
 dbSNP
2g.47410181dupCA658683186MSH2c.454dup (p.Met152AsnfsTer5)
c.256dup (p.Met86AsnfsTer5)
n.526dup
n.516dup
 ClinVar dbSNP
2g.47410181delCA021176MSH2c.454del (p.Met152CysfsTer22)
c.256del (p.Met86CysfsTer22)
n.526del
n.516del
 ClinVar dbSNP
2g.47410180_47410181delCA2586969166MSH2c.453_454del (p.Lys151AsnfsTer5)
c.255_256del (p.Lys85AsnfsTer5)
n.525_526del
n.515_516del
2g.47410179A=CA2495831189MSH2c.452A= (p.Lys151=)
c.254A= (p.Lys85=)
n.524A=
n.514A=
2g.47410179A>CCA346730491MSH2c.452A>C (p.Lys151Thr)
c.254A>C (p.Lys85Thr)
n.524A>C
n.514A>C
 ClinVar dbSNP
2g.47410179A>GCA346730492MSH2c.452A>G (p.Lys151Arg)
c.254A>G (p.Lys85Arg)
n.524A>G
n.514A>G
 dbSNP gnomAD v4
2g.47410179A>TCA346730493MSH2c.452A>T (p.Lys151Ile)
c.254A>T (p.Lys85Ile)
n.524A>T
n.514A>T
 dbSNP
2g.47410180A>CCA346730494MSH2c.453A>C (p.Lys151Asn)
c.255A>C (p.Lys85Asn)
n.525A>C
n.515A>C
 dbSNP
2g.47410180A>GCA426119493MSH2c.453A>G (p.Lys151=)
c.255A>G (p.Lys85=)
n.525A>G
n.515A>G
 ClinVar
2g.47410180A>TCA346730495MSH2c.453A>T (p.Lys151Asn)
c.255A>T (p.Lys85Asn)
n.525A>T
n.515A>T
 dbSNP
2g.47410181A>CCA346730496MSH2c.454A>C (p.Met152Leu)
c.256A>C (p.Met86Leu)
n.526A>C
n.516A>C
 dbSNP
2g.47410181A>GCA346730497MSH2c.454A>G (p.Met152Val)
c.256A>G (p.Met86Val)
n.526A>G
n.516A>G
2g.47410181A>TCA346730498MSH2c.454A>T (p.Met152Leu)
c.256A>T (p.Met86Leu)
n.526A>T
n.516A>T
2g.47410182T>ACA346730499MSH2c.455T>A (p.Met152Lys)
c.257T>A (p.Met86Lys)
n.527T>A
n.517T>A
 dbSNP
2g.47410182T>CCA346730500MSH2c.455T>C (p.Met152Thr)
c.257T>C (p.Met86Thr)
n.527T>C
n.517T>C
2g.47410182T>GCA346730501MSH2c.455T>G (p.Met152Arg)
c.257T>G (p.Met86Arg)
n.527T>G
n.517T>G
 dbSNP
2g.47410183G>ACA346730504MSH2c.456G>A (p.Met152Ile)
c.258G>A (p.Met86Ile)
n.528G>A
n.518G>A
 ClinVar dbSNP
2g.47410183G>CCA346730503MSH2c.456G>C (p.Met152Ile)
c.258G>C (p.Met86Ile)
n.528G>C
n.518G>C
 dbSNP
2g.47410183G=CA2495831190MSH2c.456G= (p.Met152=)
c.258G= (p.Met86=)
n.528G=
n.518G=
2g.47410183G>TCA346730502MSH2c.456G>T (p.Met152Ile)
c.258G>T (p.Met86Ile)
n.528G>T
n.518G>T

Number of alleles fetched