Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47411348_47413406delCA658760710MSH2c.645+976_792+846del
c.447+976_594+846del
n.717+976_864+846del
n.707+976_854+846del
2g.47412371_47412373delCA2658946214MSH2c.646-43_646-41del (n.646-43_646-41del)
c.448-43_448-41del (n.448-43_448-41del)
n.718-43_718-41del
n.708-43_708-41del
 gnomAD v4
2g.47412374C>ACA2658946216MSH2c.646-40C>A (n.646-40C>A)
c.448-40C>A (n.448-40C>A)
n.718-40C>A
n.708-40C>A
 gnomAD v4
2g.47412374C=CA2495832628MSH2c.646-40C= (n.646-40C=)
c.448-40C= (n.448-40C=)
n.718-40C=
n.708-40C=
2g.47412374C>GCA46680983MSH2c.646-40C>G (n.646-40C>G)
c.448-40C>G (n.448-40C>G)
n.718-40C>G
n.708-40C>G
 dbSNP gnomAD v4
2g.47412374C>TCA039886MSH2c.646-40C>T (n.646-40C>T)
c.448-40C>T (n.448-40C>T)
n.718-40C>T
n.708-40C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412375C>ACA2658946217MSH2c.646-39C>A (n.646-39C>A)
c.448-39C>A (n.448-39C>A)
n.718-39C>A
n.708-39C>A
 gnomAD v4
2g.47412375C>TCA2699266833MSH2c.646-39C>T (n.646-39C>T)
c.448-39C>T (n.448-39C>T)
n.718-39C>T
n.708-39C>T
 dbSNP
2g.47412376T>CCA2658946219MSH2c.646-38T>C (n.646-38T>C)
c.448-38T>C (n.448-38T>C)
n.718-38T>C
n.708-38T>C
 dbSNP gnomAD v4
2g.47412379delCA2658946218MSH2c.646-35del (n.646-35del)
c.448-35del (n.448-35del)
n.718-35del
n.708-35del
 gnomAD v4
2g.47412377T>CCA532705146MSH2c.646-37T>C (n.646-37T>C)
c.448-37T>C (n.448-37T>C)
n.718-37T>C
n.708-37T>C
 dbSNP gnomAD v2 gnomAD v4
2g.47412377T=CA2495832629MSH2c.646-37T= (n.646-37T=)
c.448-37T= (n.448-37T=)
n.718-37T=
n.708-37T=
2g.47412378T>ACA2658946220MSH2c.646-36T>A (n.646-36T>A)
c.448-36T>A (n.448-36T>A)
n.718-36T>A
n.708-36T>A
 gnomAD v4
2g.47412378T>CCA2699266876MSH2c.646-36T>C (n.646-36T>C)
c.448-36T>C (n.448-36T>C)
n.718-36T>C
n.708-36T>C
 dbSNP
2g.47412379T>CCA532705147MSH2c.646-35T>C (n.646-35T>C)
c.448-35T>C (n.448-35T>C)
n.718-35T>C
n.708-35T>C
 dbSNP gnomAD v2 gnomAD v4
2g.47412379T=CA2495832630MSH2c.646-35T= (n.646-35T=)
c.448-35T= (n.448-35T=)
n.718-35T=
n.708-35T=
2g.47412380C=CA2495832631MSH2c.646-34C= (n.646-34C=)
c.448-34C= (n.448-34C=)
n.718-34C=
n.708-34C=
2g.47412380C>GCA2658946221MSH2c.646-34C>G (n.646-34C>G)
c.448-34C>G (n.448-34C>G)
n.718-34C>G
n.708-34C>G
 dbSNP gnomAD v4
2g.47412380C>TCA2495832632MSH2c.646-34C>T (n.646-34C>T)
c.448-34C>T (n.448-34C>T)
n.718-34C>T
n.708-34C>T
 dbSNP gnomAD v4
2g.47412382C>ACA2658946222MSH2c.646-32C>A (n.646-32C>A)
c.448-32C>A (n.448-32C>A)
n.718-32C>A
n.708-32C>A
 gnomAD v4
2g.47412382C=CA2495832633MSH2c.646-32C= (n.646-32C=)
c.448-32C= (n.448-32C=)
n.718-32C=
n.708-32C=
2g.47412382C>GCA2699080521MSH2c.646-32C>G (n.646-32C>G)
c.448-32C>G (n.448-32C>G)
n.718-32C>G
n.708-32C>G
 dbSNP
2g.47412382C>TCA1649258MSH2c.646-32C>T (n.646-32C>T)
c.448-32C>T (n.448-32C>T)
n.718-32C>T
n.708-32C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412382_47412385delinsCATACA2495832634MSH2c.646-32_646-29delinsCATA (n.646-32_646-29delinsCATA)
c.448-32_448-29delinsCATA (n.448-32_448-29delinsCATA)
n.718-32_718-29delinsCATA
n.708-32_708-29delinsCATA
2g.47412383A=CA2495832635MSH2c.646-31A= (n.646-31A=)
c.448-31A= (n.448-31A=)
n.718-31A=
n.708-31A=
2g.47412383A>CCA2495832636MSH2c.646-31A>C (n.646-31A>C)
c.448-31A>C (n.448-31A>C)
n.718-31A>C
n.708-31A>C
 dbSNP gnomAD v4
2g.47412383A>GCA532705148MSH2c.646-31A>G (n.646-31A>G)
c.448-31A>G (n.448-31A>G)
n.718-31A>G
n.708-31A>G
 dbSNP gnomAD v2 gnomAD v4
2g.47412383A>TCA039852MSH2c.646-31A>T (n.646-31A>T)
c.448-31A>T (n.448-31A>T)
n.718-31A>T
n.708-31A>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412383_47412385delCA1649257MSH2c.646-31_646-29del (n.646-31_646-29del)
c.448-31_448-29del (n.448-31_448-29del)
n.718-31_718-29del
n.708-31_708-29del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412384T>CCA769453473MSH2c.646-30T>C (n.646-30T>C)
c.448-30T>C (n.448-30T>C)
n.718-30T>C
n.708-30T>C
 dbSNP gnomAD v4
2g.47412384T=CA2495832637MSH2c.646-30T= (n.646-30T=)
c.448-30T= (n.448-30T=)
n.718-30T=
n.708-30T=
2g.47412385A=CA2495832638MSH2c.646-29A= (n.646-29A=)
c.448-29A= (n.448-29A=)
n.718-29A=
n.708-29A=
2g.47412385A>GCA46681025MSH2c.646-29A>G (n.646-29A>G)
c.448-29A>G (n.448-29A>G)
n.718-29A>G
n.708-29A>G
 dbSNP gnomAD v4
2g.47412385A>TCA2495832639MSH2c.646-29A>T (n.646-29A>T)
c.448-29A>T (n.448-29A>T)
n.718-29A>T
n.708-29A>T
 dbSNP gnomAD v4
2g.47412386G>ACA2699121105MSH2c.646-28G>A (n.646-28G>A)
c.448-28G>A (n.448-28G>A)
n.718-28G>A
n.708-28G>A
 dbSNP
2g.47412386G>CCA2495832641MSH2c.646-28G>C (n.646-28G>C)
c.448-28G>C (n.448-28G>C)
n.718-28G>C
n.708-28G>C
 dbSNP
2g.47412386G=CA2495832640MSH2c.646-28G= (n.646-28G=)
c.448-28G= (n.448-28G=)
n.718-28G=
n.708-28G=
2g.47412386G>TCA2658946223MSH2c.646-28G>T (n.646-28G>T)
c.448-28G>T (n.448-28G>T)
n.718-28G>T
n.708-28G>T
 gnomAD v4
2g.47412387T>ACA2699266878MSH2c.646-27T>A (n.646-27T>A)
c.448-27T>A (n.448-27T>A)
n.718-27T>A
n.708-27T>A
 dbSNP
2g.47412389_47412393delCA2749801325MSH2c.646-25_646-21del (n.646-25_646-21del)
c.448-25_448-21del (n.448-25_448-21del)
n.718-25_718-21del
n.708-25_708-21del
2g.47412388A=CA2495832642MSH2c.646-26A= (n.646-26A=)
c.448-26A= (n.448-26A=)
n.718-26A=
n.708-26A=
2g.47412388A>CCA2658946224MSH2c.646-26A>C (n.646-26A>C)
c.448-26A>C (n.448-26A>C)
n.718-26A>C
n.708-26A>C
 gnomAD v4
2g.47412388A>GCA532705149MSH2c.646-26A>G (n.646-26A>G)
c.448-26A>G (n.448-26A>G)
n.718-26A>G
n.708-26A>G
 dbSNP gnomAD v2 gnomAD v4
2g.47412388A>TCA2699099890MSH2c.646-26A>T (n.646-26A>T)
c.448-26A>T (n.448-26A>T)
n.718-26A>T
n.708-26A>T
 dbSNP
2g.47412389G=CA2495832643MSH2c.646-25G= (n.646-25G=)
c.448-25G= (n.448-25G=)
n.718-25G=
n.708-25G=
2g.47412389G>TCA532705150MSH2c.646-25G>T (n.646-25G>T)
c.448-25G>T (n.448-25G>T)
n.718-25G>T
n.708-25G>T
 dbSNP gnomAD v2 gnomAD v4
2g.47412391T>ACA2699082441MSH2c.646-23T>A (n.646-23T>A)
c.448-23T>A (n.448-23T>A)
n.718-23T>A
n.708-23T>A
 dbSNP
2g.47412391T>CCA2658946225MSH2c.646-23T>C (n.646-23T>C)
c.448-23T>C (n.448-23T>C)
n.718-23T>C
n.708-23T>C
 dbSNP gnomAD v4
2g.47412391T>GCA039834MSH2c.646-23T>G (n.646-23T>G)
c.448-23T>G (n.448-23T>G)
n.718-23T>G
n.708-23T>G
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412391T=CA2495832644MSH2c.646-23T= (n.646-23T=)
c.448-23T= (n.448-23T=)
n.718-23T=
n.708-23T=
2g.47412392T>CCA2658946226MSH2c.646-22T>C (n.646-22T>C)
c.448-22T>C (n.448-22T>C)
n.718-22T>C
n.708-22T>C
 gnomAD v4
2g.47412393A=CA2495832645MSH2c.646-21A= (n.646-21A=)
c.448-21A= (n.448-21A=)
n.718-21A=
n.708-21A=
2g.47412393A>GCA532705151MSH2c.646-21A>G (n.646-21A>G)
c.448-21A>G (n.448-21A>G)
n.718-21A>G
n.708-21A>G
 dbSNP gnomAD v2 gnomAD v4
2g.47412393A>TCA2576960701MSH2c.646-21A>T (n.646-21A>T)
c.448-21A>T (n.448-21A>T)
n.718-21A>T
n.708-21A>T
 dbSNP gnomAD v4
2g.47412395delCA2699266889MSH2c.646-19del (n.646-19del)
c.448-19del (n.448-19del)
n.718-19del
n.708-19del
 dbSNP
2g.47412394A>GCA2573134696MSH2c.646-20A>G (n.646-20A>G)
c.448-20A>G (n.448-20A>G)
n.718-20A>G
n.708-20A>G
 ClinVar dbSNP
2g.47412394A>TCA2580066576MSH2c.646-20A>T (n.646-20A>T)
c.448-20A>T (n.448-20A>T)
n.718-20A>T
n.708-20A>T
 ClinVar
2g.47412395A>TCA2699266963MSH2c.646-19A>T (n.646-19A>T)
c.448-19A>T (n.448-19A>T)
n.718-19A>T
n.708-19A>T
 dbSNP
2g.47412395_47412429delCA2580066579MSH2c.646-19_661del
c.448-19_463del
n.718-19_733del
n.708-19_723del
 ClinVar
2g.47412396C=CA2495832646MSH2c.646-18C= (n.646-18C=)
c.448-18C= (n.448-18C=)
n.718-18C=
n.708-18C=
2g.47412396C>GCA039826MSH2c.646-18C>G (n.646-18C>G)
c.448-18C>G (n.448-18C>G)
n.718-18C>G
n.708-18C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412396C>TCA2658946227MSH2c.646-18C>T (n.646-18C>T)
c.448-18C>T (n.448-18C>T)
n.718-18C>T
n.708-18C>T
 dbSNP gnomAD v4
2g.47412397T>CCA2699266984MSH2c.646-17T>C (n.646-17T>C)
c.448-17T>C (n.448-17T>C)
n.718-17T>C
n.708-17T>C
 dbSNP
2g.47412397T>GCA2699266970MSH2c.646-17T>G (n.646-17T>G)
c.448-17T>G (n.448-17T>G)
n.718-17T>G
n.708-17T>G
 dbSNP
2g.47412398A=CA2495832647MSH2c.646-16A= (n.646-16A=)
c.448-16A= (n.448-16A=)
n.718-16A=
n.708-16A=
2g.47412398A>CCA2658946228MSH2c.646-16A>C (n.646-16A>C)
c.448-16A>C (n.448-16A>C)
n.718-16A>C
n.708-16A>C
 gnomAD v4
2g.47412398A>GCA16604223MSH2c.646-16A>G (n.646-16A>G)
c.448-16A>G (n.448-16A>G)
n.718-16A>G
n.708-16A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412398A>TCA021666MSH2c.646-16A>T (n.646-16A>T)
c.448-16A>T (n.448-16A>T)
n.718-16A>T
n.708-16A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412398_47412400delinsATTCA2495832648MSH2c.646-16_646-14delinsATT (n.646-16_646-14delinsATT)
c.448-16_448-14delinsATT (n.448-16_448-14delinsATT)
n.718-16_718-14delinsATT
n.708-16_708-14delinsATT
2g.47412399T>CCA039801MSH2c.646-15T>C (n.646-15T>C)
c.448-15T>C (n.448-15T>C)
n.718-15T>C
n.708-15T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412399T=CA2495832649MSH2c.646-15T= (n.646-15T=)
c.448-15T= (n.448-15T=)
n.718-15T=
n.708-15T=
2g.47412400_47412401delCA658683201MSH2c.646-14_646-13del (n.646-14_646-13del)
c.448-14_448-13del (n.448-14_448-13del)
n.718-14_718-13del
n.708-14_708-13del
 ClinVar dbSNP
2g.47412401T>CCA039794MSH2c.646-13T>C (n.646-13T>C)
c.448-13T>C (n.448-13T>C)
n.718-13T>C
n.708-13T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412401T=CA2495832650MSH2c.646-13T= (n.646-13T=)
c.448-13T= (n.448-13T=)
n.718-13T=
n.708-13T=
2g.47412402C>ACA2658946229MSH2c.646-12C>A (n.646-12C>A)
c.448-12C>A (n.448-12C>A)
n.718-12C>A
n.708-12C>A
 gnomAD v4
2g.47412402C>GCA2499215986MSH2c.646-12C>G (n.646-12C>G)
c.448-12C>G (n.448-12C>G)
n.718-12C>G
n.708-12C>G
 ClinVar dbSNP
2g.47412402C>TCA2697548108MSH2c.646-12C>T (n.646-12C>T)
c.448-12C>T (n.448-12C>T)
n.718-12C>T
n.708-12C>T
 ClinVar dbSNP
2g.47412403T>CCA10584208MSH2c.646-11T>C (n.646-11T>C)
c.448-11T>C (n.448-11T>C)
n.718-11T>C
n.708-11T>C
 ClinVar dbSNP gnomAD v4
2g.47412403T=CA2495832651MSH2c.646-11T= (n.646-11T=)
c.448-11T= (n.448-11T=)
n.718-11T=
n.708-11T=
2g.47412403_47412417delinsTTTCAAAATAGATAACA2495832652MSH2c.646-11_649delinsTTTCAAAATAGATAA
c.448-11_451delinsTTTCAAAATAGATAA
n.718-11_721delinsTTTCAAAATAGATAA
n.708-11_711delinsTTTCAAAATAGATAA
2g.47412404T>CCA2658946230MSH2c.646-10T>C (n.646-10T>C)
c.448-10T>C (n.448-10T>C)
n.718-10T>C
n.708-10T>C
 dbSNP gnomAD v4
2g.47412410_47412423delCA645369189MSH2c.646-4_655del
c.448-4_457del
n.718-4_727del
n.708-4_717del
 ClinVar dbSNP
2g.47412405T>ACA2699267406MSH2c.646-9T>A (n.646-9T>A)
c.448-9T>A (n.448-9T>A)
n.718-9T>A
n.708-9T>A
 dbSNP
2g.47412405_47412406delinsTCCA2495832653MSH2c.646-9_646-8delinsTC (n.646-9_646-8delinsTC)
c.448-9_448-8delinsTC (n.448-9_448-8delinsTC)
n.718-9_718-8delinsTC
n.708-9_708-8delinsTC
2g.47412406delCA10581998MSH2c.646-8del (n.646-8del)
c.448-8del (n.448-8del)
n.718-8del
n.708-8del
 ClinVar dbSNP
2g.47412406C>ACA2495832655MSH2c.646-8C>A (n.646-8C>A)
c.448-8C>A (n.448-8C>A)
n.718-8C>A
n.708-8C>A
 ClinVar dbSNP gnomAD v4
2g.47412406C=CA2495832654MSH2c.646-8C= (n.646-8C=)
c.448-8C= (n.448-8C=)
n.718-8C=
n.708-8C=
2g.47412406C>GCA2658946231MSH2c.646-8C>G (n.646-8C>G)
c.448-8C>G (n.448-8C>G)
n.718-8C>G
n.708-8C>G
 dbSNP gnomAD v4
2g.47412406C>TCA2580066587MSH2c.646-8C>T (n.646-8C>T)
c.448-8C>T (n.448-8C>T)
n.718-8C>T
n.708-8C>T
 ClinVar gnomAD v4
2g.47412410dupCA658655702MSH2c.646-4dup (n.646-4dup)
c.448-4dup (n.448-4dup)
n.718-4dup
n.708-4dup
 ClinVar dbSNP
2g.47412409_47412423delCA2695200755MSH2c.646-5_655del
c.448-5_457del
n.718-5_727del
n.708-5_717del
 ClinVar
2g.47412408A=CA2495832657MSH2c.646-6A= (n.646-6A=)
c.448-6A= (n.448-6A=)
n.718-6A=
n.708-6A=
2g.47412408A>GCA658683202MSH2c.646-6A>G (n.646-6A>G)
c.448-6A>G (n.448-6A>G)
n.718-6A>G
n.708-6A>G
 ClinVar dbSNP
2g.47412408_47412420delinsAAATAGATAATTCCA2495832656MSH2c.646-6_652delinsAAATAGATAATTC
c.448-6_454delinsAAATAGATAATTC
n.718-6_724delinsAAATAGATAATTC
n.708-6_714delinsAAATAGATAATTC
2g.47412411_47412447dupCA2499215987MSH2c.646-3_679dup
c.448-3_481dup
n.718-3_751dup
n.708-3_741dup
 ClinVar dbSNP
2g.47412408_47412495delCA2580066592MSH2c.646-6_727del
c.448-6_529del
n.718-6_799del
n.708-6_789del
 ClinVar
2g.47412409A=CA2495832659MSH2c.646-5A= (n.646-5A=)
c.448-5A= (n.448-5A=)
n.718-5A=
n.708-5A=
2g.47412409A>CCA2573134697MSH2c.646-5A>C (n.646-5A>C)
c.448-5A>C (n.448-5A>C)
n.718-5A>C
n.708-5A>C
 ClinVar dbSNP
2g.47412409A>TCA532705152MSH2c.646-5A>T (n.646-5A>T)
c.448-5A>T (n.448-5A>T)
n.718-5A>T
n.708-5A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412409_47412413delinsAATAGCA2495832658MSH2c.646-5_646-1delinsAATAG (n.646-5_646-1delinsAATAG)
c.448-5_448-1delinsAATAG (n.448-5_448-1delinsAATAG)
n.718-5_718-1delinsAATAG
n.708-5_708-1delinsAATAG
2g.47412411_47412422delCA331656MSH2c.646-3_654del
c.448-3_456del
n.718-3_726del
n.708-3_716del
 ClinVar dbSNP
2g.47412410A=CA2495832660MSH2c.646-4A= (n.646-4A=)
c.448-4A= (n.448-4A=)
n.718-4A=
n.708-4A=
2g.47412410A>GCA021683MSH2c.646-4A>G (n.646-4A>G)
c.448-4A>G (n.448-4A>G)
n.718-4A>G
n.708-4A>G
 ClinVar dbSNP gnomAD v4
2g.47412410A>TCA2699080523MSH2c.646-4A>T (n.646-4A>T)
c.448-4A>T (n.448-4A>T)
n.718-4A>T
n.708-4A>T
 dbSNP
2g.47412413_47412416delCA645372531MSH2c.646-1_648del
c.448-1_450del
n.718-1_720del
n.708-1_710del
 ClinVar dbSNP
2g.47412413_47413046delCA2499215988MSH2c.646-1_792+486del
c.448-1_594+486del
n.718-1_864+486del
n.708-1_854+486del
 ClinVar dbSNP
2g.47412411T>ACA2699076647MSH2c.646-3T>A (n.646-3T>A)
c.448-3T>A (n.448-3T>A)
n.718-3T>A
n.708-3T>A
 dbSNP
2g.47412411T>CCA039878MSH2c.646-3T>C (n.646-3T>C)
c.448-3T>C (n.448-3T>C)
n.718-3T>C
n.708-3T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412411T>GCA021679MSH2c.646-3T>G (n.646-3T>G)
c.448-3T>G (n.448-3T>G)
n.718-3T>G
n.708-3T>G
 ClinVar dbSNP
2g.47412411T=CA2495832661MSH2c.646-3T= (n.646-3T=)
c.448-3T= (n.448-3T=)
n.718-3T=
n.708-3T=
2g.47412412A=CA2495832662MSH2c.646-2A= (n.646-2A=)
c.448-2A= (n.448-2A=)
n.718-2A=
n.708-2A=
2g.47412412A>CCA346731597MSH2c.646-2A>C (n.646-2A>C)
c.448-2A>C (n.448-2A>C)
n.718-2A>C
n.708-2A>C
 ClinVar dbSNP
2g.47412412A>GCA021672MSH2c.646-2A>G (n.646-2A>G)
c.448-2A>G (n.448-2A>G)
n.718-2A>G
n.708-2A>G
 ClinVar dbSNP gnomAD v4
2g.47412412A>TCA346731602MSH2c.646-2A>T (n.646-2A>T)
c.448-2A>T (n.448-2A>T)
n.718-2A>T
n.708-2A>T
 ClinVar dbSNP COSMIC
2g.47412413G>ACA346731606MSH2c.646-1G>A (n.646-1G>A)
c.448-1G>A (n.448-1G>A)
n.718-1G>A
n.708-1G>A
 ClinVar dbSNP
2g.47412413G>CCA346731609MSH2c.646-1G>C (n.646-1G>C)
c.448-1G>C (n.448-1G>C)
n.718-1G>C
n.708-1G>C
 ClinVar dbSNP
2g.47412413G=CA2495832663MSH2c.646-1G= (n.646-1G=)
c.448-1G= (n.448-1G=)
n.718-1G=
n.708-1G=
2g.47412413G>TCA346731612MSH2c.646-1G>T (n.646-1G>T)
c.448-1G>T (n.448-1G>T)
n.718-1G>T
n.708-1G>T
 ClinVar dbSNP COSMIC
2g.47412413_47412416delinsGATACA2495832664MSH2c.646-1_648delinsGATA
c.448-1_450delinsGATA
n.718-1_720delinsGATA
n.708-1_710delinsGATA
2g.47412414A=CA2495832665MSH2c.646A= (p.Ile216=)
c.448A= (p.Ile150=)
n.718A=
n.708A=
2g.47412414A>CCA039951MSH2c.646A>C (p.Ile216Leu)
c.448A>C (p.Ile150Leu)
n.718A>C
n.708A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412414A>GCA021692MSH2c.646A>G (p.Ile216Val)
c.448A>G (p.Ile150Val)
n.718A>G
n.708A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412414A>TCA346731616MSH2c.646A>T (p.Ile216Leu)
c.448A>T (p.Ile150Leu)
n.718A>T
n.708A>T
 ClinVar dbSNP
2g.47412415_47412416dupCA2586969187MSH2c.647_648dup (p.Ile217Ter)
c.449_450dup (p.Ile151Ter)
n.719_720dup
n.709_710dup
2g.47412416_47412418delCA658683203MSH2c.648_650del (p.Ile217del)
c.450_452del (p.Ile151del)
n.720_722del
n.710_712del
 ClinVar dbSNP
2g.47412415delCA2576960719MSH2c.647del (p.Ile216LysfsTer8)
c.449del (p.Ile150LysfsTer8)
n.719del
n.709del
 ClinVar
2g.47412415T>ACA346731625MSH2c.647T>A (p.Ile216Lys)
c.449T>A (p.Ile150Lys)
n.719T>A
n.709T>A
2g.47412415T>CCA021697MSH2c.647T>C (p.Ile216Thr)
c.449T>C (p.Ile150Thr)
n.719T>C
n.709T>C
 ClinVar dbSNP gnomAD v4
2g.47412415T>GCA346731629MSH2c.647T>G (p.Ile216Arg)
c.449T>G (p.Ile150Arg)
n.719T>G
n.709T>G
2g.47412415T=CA2495832667MSH2c.647T= (p.Ile216=)
c.449T= (p.Ile150=)
n.719T=
n.709T=
2g.47412415dupCA2580066599MSH2c.647dup (p.Ile217AsnfsTer15)
c.449dup (p.Ile151AsnfsTer15)
n.719dup
n.709dup
 ClinVar
2g.47412415_47412420delinsTAATTCCA2495832666MSH2c.647_652delinsTAATTC (p.Ile216=)
c.449_454delinsTAATTC (p.Ile150=)
n.719_724delinsTAATTC
n.709_714delinsTAATTC
2g.47412415_47412416insTGCA2580066602MSH2c.647_648insTG (p.Ile217GlufsTer8)
c.449_450insTG (p.Ile151GlufsTer8)
n.719_720insTG
n.709_710insTG
 ClinVar
2g.47412416A=CA2495832668MSH2c.648A= (p.Ile216=)
c.450A= (p.Ile150=)
n.720A=
n.710A=
2g.47412416A>CCA425967217MSH2c.648A>C (p.Ile216=)
c.450A>C (p.Ile150=)
n.720A>C
n.710A>C
2g.47412416A>GCA346731632MSH2c.648A>G (p.Ile216Met)
c.450A>G (p.Ile150Met)
n.720A>G
n.710A>G
2g.47412416A>TCA425967234MSH2c.648A>T (p.Ile216=)
c.450A>T (p.Ile150=)
n.720A>T
n.710A>T
 dbSNP gnomAD v2 gnomAD v4
2g.47412417dupCA2586969189MSH2c.649dup (p.Ile217AsnfsTer15)
c.451dup (p.Ile151AsnfsTer15)
n.721dup
n.711dup
2g.47412416_47412417dupCA2580066603MSH2c.648_649dup (p.Ile217LysfsTer8)
c.450_451dup (p.Ile151LysfsTer8)
n.720_721dup
n.710_711dup
 ClinVar
2g.47412418_47412422delCA021704MSH2c.650_654del (p.Ile217LysfsTer13)
c.452_456del (p.Ile151LysfsTer13)
n.722_726del
n.712_716del
 ClinVar dbSNP
2g.47412417A=CA2495832669MSH2c.649A= (p.Ile217=)
c.451A= (p.Ile151=)
n.721A=
n.711A=
2g.47412417A>CCA346731637MSH2c.649A>C (p.Ile217Leu)
c.451A>C (p.Ile151Leu)
n.721A>C
n.711A>C
 dbSNP
2g.47412417A>GCA039965MSH2c.649A>G (p.Ile217Val)
c.451A>G (p.Ile151Val)
n.721A>G
n.711A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412417A>TCA346731639MSH2c.649A>T (p.Ile217Phe)
c.451A>T (p.Ile151Phe)
n.721A>T
n.711A>T
2g.47412418T>ACA346731642MSH2c.650T>A (p.Ile217Asn)
c.452T>A (p.Ile151Asn)
n.722T>A
n.712T>A
 dbSNP
2g.47412418T>CCA346731645MSH2c.650T>C (p.Ile217Thr)
c.452T>C (p.Ile151Thr)
n.722T>C
n.712T>C
2g.47412418T>GCA346731648MSH2c.650T>G (p.Ile217Ser)
c.452T>G (p.Ile151Ser)
n.722T>G
n.712T>G
2g.47412419T>ACA425967255MSH2c.651T>A (p.Ile217=)
c.453T>A (p.Ile151=)
n.723T>A
n.713T>A
 ClinVar dbSNP
2g.47412419T>CCA425967251MSH2c.651T>C (p.Ile217=)
c.453T>C (p.Ile151=)
n.723T>C
n.713T>C
2g.47412419T>GCA346731652MSH2c.651T>G (p.Ile217Met)
c.453T>G (p.Ile151Met)
n.723T>G
n.713T>G
2g.47412420C>ACA346731664MSH2c.652C>A (p.Gln218Lys)
c.454C>A (p.Gln152Lys)
n.724C>A
n.714C>A
 ClinVar dbSNP gnomAD v4
2g.47412420C=CA2495832670MSH2c.652C= (p.Gln218=)
c.454C= (p.Gln152=)
n.724C=
n.714C=
2g.47412420C>GCA346731668MSH2c.652C>G (p.Gln218Glu)
c.454C>G (p.Gln152Glu)
n.724C>G
n.714C>G
 ClinVar dbSNP gnomAD v4
2g.47412420C>TCA021710MSH2c.652C>T (p.Gln218Ter)
c.454C>T (p.Gln152Ter)
n.724C>T
n.714C>T
 ClinVar dbSNP
2g.47412421A>CCA346731677MSH2c.653A>C (p.Gln218Pro)
c.455A>C (p.Gln152Pro)
n.725A>C
n.715A>C
2g.47412421A>GCA346731675MSH2c.653A>G (p.Gln218Arg)
c.455A>G (p.Gln152Arg)
n.725A>G
n.715A>G
 dbSNP gnomAD v4
2g.47412421A>TCA346731674MSH2c.653A>T (p.Gln218Leu)
c.455A>T (p.Gln152Leu)
n.725A>T
n.715A>T
2g.47412423dupCA891842933MSH2c.655dup (p.Arg219LysfsTer13)
c.457dup (p.Arg153LysfsTer13)
n.727dup
n.717dup
 ClinVar dbSNP
2g.47412422A=CA2495832671MSH2c.654A= (p.Gln218=)
c.456A= (p.Gln152=)
n.726A=
n.716A=
2g.47412422A>CCA346731681MSH2c.654A>C (p.Gln218His)
c.456A>C (p.Gln152His)
n.726A>C
n.716A>C
2g.47412422A>GCA46681145MSH2c.654A>G (p.Gln218=)
c.456A>G (p.Gln152=)
n.726A>G
n.716A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412422A>TCA346731684MSH2c.654A>T (p.Gln218His)
c.456A>T (p.Gln152His)
n.726A>T
n.716A>T
2g.47412423A=CA2495832673MSH2c.655A= (p.Arg219=)
c.457A= (p.Arg153=)
n.727A=
n.717A=
2g.47412423A>CCA425967282MSH2c.655A>C (p.Arg219=)
c.457A>C (p.Arg153=)
n.727A>C
n.717A>C
 ClinVar dbSNP gnomAD v4
2g.47412423A>GCA346731685MSH2c.655A>G (p.Arg219Gly)
c.457A>G (p.Arg153Gly)
n.727A>G
n.717A>G
 gnomAD v4
2g.47412423A>TCA346731686MSH2c.655A>T (p.Arg219Ter)
c.457A>T (p.Arg153Ter)
n.727A>T
n.717A>T
 ClinVar
2g.47412425_47412426delCA2580611300MSH2c.657_658del (p.Gly220ArgfsTer11)
c.459_460del (p.Gly154ArgfsTer11)
n.729_730del
n.719_720del
 ClinVar
2g.47412423_47412432delinsAGAGGAGGAACA2495832672MSH2c.655_664delinsAGAGGAGGAA (p.Arg219=)
c.457_466delinsAGAGGAGGAA (p.Arg153=)
n.727_736delinsAGAGGAGGAA
n.717_726delinsAGAGGAGGAA
2g.47412424G>ACA346731687MSH2c.656G>A (p.Arg219Lys)
c.458G>A (p.Arg153Lys)
n.728G>A
n.718G>A
 dbSNP gnomAD v4
2g.47412424G>CCA10581999MSH2c.656G>C (p.Arg219Thr)
c.458G>C (p.Arg153Thr)
n.728G>C
n.718G>C
 ClinVar dbSNP
2g.47412424G=CA2495832674MSH2c.656G= (p.Arg219=)
c.458G= (p.Arg153=)
n.728G=
n.718G=
2g.47412424G>TCA346731689MSH2c.656G>T (p.Arg219Ile)
c.458G>T (p.Arg153Ile)
n.728G>T
n.718G>T
2g.47412424_47412432delinsATAGATAATTTCTCA2695200756MSH2c.656_664delinsATAGATAATTTCT (p.Arg219AsnfsTer3)
c.458_466delinsATAGATAATTTCT (p.Arg153AsnfsTer3)
n.728_736delinsATAGATAATTTCT
n.718_726delinsATAGATAATTTCT
 ClinVar
2g.47412425delCA2580066608MSH2c.657del (p.Gly220GlufsTer4)
c.459del (p.Gly154GlufsTer4)
n.729del
n.719del
 ClinVar
2g.47412425A>CCA346731690MSH2c.657A>C (p.Arg219Ser)
c.459A>C (p.Arg153Ser)
n.729A>C
n.719A>C
2g.47412425A>GCA425967289MSH2c.657A>G (p.Arg219=)
c.459A>G (p.Arg153=)
n.729A>G
n.719A>G
 ClinVar dbSNP
2g.47412425A>TCA346731693MSH2c.657A>T (p.Arg219Ser)
c.459A>T (p.Arg153Ser)
n.729A>T
n.719A>T
2g.47412426G>ACA346731695MSH2c.658G>A (p.Gly220Arg)
c.460G>A (p.Gly154Arg)
n.730G>A
n.720G>A
 dbSNP
2g.47412426G>CCA346731698MSH2c.658G>C (p.Gly220Arg)
c.460G>C (p.Gly154Arg)
n.730G>C
n.720G>C
 ClinVar dbSNP
2g.47412426G=CA2495832675MSH2c.658G= (p.Gly220=)
c.460G= (p.Gly154=)
n.730G=
n.720G=
2g.47412426G>TCA346731701MSH2c.658G>T (p.Gly220Ter)
c.460G>T (p.Gly154Ter)
n.730G>T
n.720G>T
 ClinVar COSMIC
2g.47412427G>ACA346731709MSH2c.659G>A (p.Gly220Glu)
c.461G>A (p.Gly154Glu)
n.731G>A
n.721G>A
 ClinVar dbSNP gnomAD v4
2g.47412427G>CCA346731707MSH2c.659G>C (p.Gly220Ala)
c.461G>C (p.Gly154Ala)
n.731G>C
n.721G>C
 dbSNP
2g.47412427G=CA2495832676MSH2c.659G= (p.Gly220=)
c.461G= (p.Gly154=)
n.731G=
n.721G=
2g.47412427G>TCA346731705MSH2c.659G>T (p.Gly220Val)
c.461G>T (p.Gly154Val)
n.731G>T
n.721G>T
 dbSNP COSMIC
2g.47412427_47412429delinsAATCA2580612944MSH2c.659_661delinsAAT (p.Gly220GlufsTer2)
c.461_463delinsAAT (p.Gly154GlufsTer2)
n.731_733delinsAAT
n.721_723delinsAAT
 ClinVar
2g.47412428A=CA2495832677MSH2c.660A= (p.Gly220=)
c.462A= (p.Gly154=)
n.732A=
n.722A=
2g.47412428A>CCA425967308MSH2c.660A>C (p.Gly220=)
c.462A>C (p.Gly154=)
n.732A>C
n.722A>C
 ClinVar
2g.47412428A>GCA425967311MSH2c.660A>G (p.Gly220=)
c.462A>G (p.Gly154=)
n.732A>G
n.722A>G
2g.47412428A>TCA425967307MSH2c.660A>T (p.Gly220=)
c.462A>T (p.Gly154=)
n.732A>T
n.722A>T
 ClinVar dbSNP
2g.47412429G>ACA346731712MSH2c.661G>A (p.Gly221Arg)
c.463G>A (p.Gly155Arg)
n.733G>A
n.723G>A
 ClinVar dbSNP
2g.47412429G>CCA346731713MSH2c.661G>C (p.Gly221Arg)
c.463G>C (p.Gly155Arg)
n.733G>C
n.723G>C
 ClinVar dbSNP COSMIC
2g.47412429G=CA2495832678MSH2c.661G= (p.Gly221=)
c.463G= (p.Gly155=)
n.733G=
n.723G=
2g.47412429G>TCA346731717MSH2c.661G>T (p.Gly221Ter)
c.463G>T (p.Gly155Ter)
n.733G>T
n.723G>T
2g.47412430delCA2573134698MSH2c.662del (p.Gly221GlufsTer3)
c.464del (p.Gly155GlufsTer3)
n.734del
n.724del
 dbSNP
2g.47412430G>ACA346731720MSH2c.662G>A (p.Gly221Glu)
c.464G>A (p.Gly155Glu)
n.734G>A
n.724G>A
 ClinVar dbSNP
2g.47412430G>CCA346731723MSH2c.662G>C (p.Gly221Ala)
c.464G>C (p.Gly155Ala)
n.734G>C
n.724G>C
 dbSNP
2g.47412430G=CA2495832679MSH2c.662G= (p.Gly221=)
c.464G= (p.Gly155=)
n.734G=
n.724G=
2g.47412430G>TCA346731725MSH2c.662G>T (p.Gly221Val)
c.464G>T (p.Gly155Val)
n.734G>T
n.724G>T
 COSMIC
2g.47412431A=CA2495832680MSH2c.663A= (p.Gly221=)
c.465A= (p.Gly155=)
n.735A=
n.725A=
2g.47412431A>CCA425967325MSH2c.663A>C (p.Gly221=)
c.465A>C (p.Gly155=)
n.735A>C
n.725A>C
2g.47412431A>GCA425967326MSH2c.663A>G (p.Gly221=)
c.465A>G (p.Gly155=)
n.735A>G
n.725A>G
 ClinVar dbSNP
2g.47412431A>TCA425967328MSH2c.663A>T (p.Gly221=)
c.465A>T (p.Gly155=)
n.735A>T
n.725A>T
 dbSNP
2g.47412432delCA425967331MSH2c.664del (p.Ile222PhefsTer2)
c.466del (p.Ile156PhefsTer2)
n.736del
n.726del
 COSMIC
2g.47412432A=CA2495832681MSH2c.664A= (p.Ile222=)
c.466A= (p.Ile156=)
n.736A=
n.726A=
2g.47412432A>CCA346731730MSH2c.664A>C (p.Ile222Leu)
c.466A>C (p.Ile156Leu)
n.736A>C
n.726A>C
 COSMIC
2g.47412432A>GCA346731733MSH2c.664A>G (p.Ile222Val)
c.466A>G (p.Ile156Val)
n.736A>G
n.726A>G
 ClinVar dbSNP gnomAD v4
2g.47412432A>TCA039981MSH2c.664A>T (p.Ile222Phe)
c.466A>T (p.Ile156Phe)
n.736A>T
n.726A>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412433T>ACA346731739MSH2c.665T>A (p.Ile222Asn)
c.467T>A (p.Ile156Asn)
n.737T>A
n.727T>A
 dbSNP
2g.47412433T>CCA16617559MSH2c.665T>C (p.Ile222Thr)
c.467T>C (p.Ile156Thr)
n.737T>C
n.727T>C
 ClinVar dbSNP
2g.47412433T>GCA346731744MSH2c.665T>G (p.Ile222Ser)
c.467T>G (p.Ile156Ser)
n.737T>G
n.727T>G
2g.47412433T=CA2495832682MSH2c.665T= (p.Ile222=)
c.467T= (p.Ile156=)
n.737T=
n.727T=
2g.47412433_47412456dupCA2580066622MSH2c.665_688dup (p.Lys229_Ala230insValLeuIleThrGluArgLysLys)
c.467_490dup (p.Lys163_Ala164insValLeuIleThrGluArgLysLys)
n.737_760dup
n.727_750dup
 ClinVar
2g.47412434T>ACA425967342MSH2c.666T>A (p.Ile222=)
c.468T>A (p.Ile156=)
n.738T>A
n.728T>A
 dbSNP
2g.47412434T>CCA425967344MSH2c.666T>C (p.Ile222=)
c.468T>C (p.Ile156=)
n.738T>C
n.728T>C
2g.47412434T>GCA346731747MSH2c.666T>G (p.Ile222Met)
c.468T>G (p.Ile156Met)
n.738T>G
n.728T>G
2g.47412435C>ACA346731751MSH2c.667C>A (p.Leu223Met)
c.469C>A (p.Leu157Met)
n.739C>A
n.729C>A
2g.47412435C=CA2495832683MSH2c.667C= (p.Leu223=)
c.469C= (p.Leu157=)
n.739C=
n.729C=
2g.47412435C>GCA346731750MSH2c.667C>G (p.Leu223Val)
c.469C>G (p.Leu157Val)
n.739C>G
n.729C>G
 ClinVar dbSNP
2g.47412435C>TCA425967354MSH2c.667C>T (p.Leu223=)
c.469C>T (p.Leu157=)
n.739C>T
n.729C>T
 ClinVar dbSNP gnomAD v4
2g.47412436T>ACA346731754MSH2c.668T>A (p.Leu223Gln)
c.470T>A (p.Leu157Gln)
n.740T>A
n.730T>A
2g.47412436T>CCA16610792MSH2c.668T>C (p.Leu223Pro)
c.470T>C (p.Leu157Pro)
n.740T>C
n.730T>C
 ClinVar dbSNP gnomAD v4
2g.47412436T>GCA346731759MSH2c.668T>G (p.Leu223Arg)
c.470T>G (p.Leu157Arg)
n.740T>G
n.730T>G
2g.47412436T=CA2495832684MSH2c.668T= (p.Leu223=)
c.470T= (p.Leu157=)
n.740T=
n.730T=
2g.47412437G>ACA039993MSH2c.669G>A (p.Leu223=)
c.471G>A (p.Leu157=)
n.741G>A
n.731G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412437G>CCA425967367MSH2c.669G>C (p.Leu223=)
c.471G>C (p.Leu157=)
n.741G>C
n.731G>C
 dbSNP gnomAD v4
2g.47412437G=CA2495832685MSH2c.669G= (p.Leu223=)
c.471G= (p.Leu157=)
n.741G=
n.731G=
2g.47412437G>TCA425967370MSH2c.669G>T (p.Leu223=)
c.471G>T (p.Leu157=)
n.741G>T
n.731G>T
 dbSNP
2g.47412438A>CCA346731769MSH2c.670A>C (p.Ile224Leu)
c.472A>C (p.Ile158Leu)
n.742A>C
n.732A>C
2g.47412438A>GCA346731772MSH2c.670A>G (p.Ile224Val)
c.472A>G (p.Ile158Val)
n.742A>G
n.732A>G
 ClinVar
2g.47412438A>TCA346731774MSH2c.670A>T (p.Ile224Phe)
c.472A>T (p.Ile158Phe)
n.742A>T
n.732A>T
 dbSNP
2g.47412439T>ACA346731778MSH2c.671T>A (p.Ile224Asn)
c.473T>A (p.Ile158Asn)
n.743T>A
n.733T>A
 dbSNP
2g.47412439T>CCA346731788MSH2c.671T>C (p.Ile224Thr)
c.473T>C (p.Ile158Thr)
n.743T>C
n.733T>C
2g.47412439T>GCA346731789MSH2c.671T>G (p.Ile224Ser)
c.473T>G (p.Ile158Ser)
n.743T>G
n.733T>G
 ClinVar dbSNP
2g.47412439T=CA2495832686MSH2c.671T= (p.Ile224=)
c.473T= (p.Ile158=)
n.743T=
n.733T=
2g.47412440C>ACA425967385MSH2c.672C>A (p.Ile224=)
c.474C>A (p.Ile158=)
n.744C>A
n.734C>A
 dbSNP gnomAD v4
2g.47412440C=CA2495832687MSH2c.672C= (p.Ile224=)
c.474C= (p.Ile158=)
n.744C=
n.734C=
2g.47412440C>GCA021724MSH2c.672C>G (p.Ile224Met)
c.474C>G (p.Ile158Met)
n.744C>G
n.734C>G
 ClinVar dbSNP gnomAD v4
2g.47412440C>TCA16604518MSH2c.672C>T (p.Ile224=)
c.474C>T (p.Ile158=)
n.744C>T
n.734C>T
 ClinVar dbSNP gnomAD v4
2g.47412441A>CCA346731795MSH2c.673A>C (p.Thr225Pro)
c.475A>C (p.Thr159Pro)
n.745A>C
n.735A>C
 ClinVar
2g.47412441A>GCA346731798MSH2c.673A>G (p.Thr225Ala)
c.475A>G (p.Thr159Ala)
n.745A>G
n.735A>G
 ClinVar dbSNP
2g.47412441A>TCA346731801MSH2c.673A>T (p.Thr225Ser)
c.475A>T (p.Thr159Ser)
n.745A>T
n.735A>T
 dbSNP
2g.47412442delCA2695200757MSH2c.674del (p.Thr225LysfsTer21)
c.476del (p.Thr159LysfsTer21)
n.746del
n.736del
 ClinVar
2g.47412442C>ACA346731806MSH2c.674C>A (p.Thr225Lys)
c.476C>A (p.Thr159Lys)
n.746C>A
n.736C>A
 dbSNP
2g.47412442C=CA2495832690MSH2c.674C= (p.Thr225=)
c.476C= (p.Thr159=)
n.746C=
n.736C=
2g.47412442C>GCA346731808MSH2c.674C>G (p.Thr225Arg)
c.476C>G (p.Thr159Arg)
n.746C>G
n.736C>G
 ClinVar dbSNP
2g.47412442C>TCA346731803MSH2c.674C>T (p.Thr225Ile)
c.476C>T (p.Thr159Ile)
n.746C>T
n.736C>T
 ClinVar dbSNP
2g.47412442_47412446delinsCAGAACA2495832689MSH2c.674_678delinsCAGAA (p.Thr225=)
c.476_480delinsCAGAA (p.Thr159=)
n.746_750delinsCAGAA
n.736_740delinsCAGAA
2g.47412442_47412447delinsCAGAAACA2495832688MSH2c.674_679delinsCAGAAA (p.Thr225=)
c.476_481delinsCAGAAA (p.Thr159=)
n.746_751delinsCAGAAA
n.736_741delinsCAGAAA
2g.47412443A>CCA425967410MSH2c.675A>C (p.Thr225=)
c.477A>C (p.Thr159=)
n.747A>C
n.737A>C
2g.47412443A>GCA425967408MSH2c.675A>G (p.Thr225=)
c.477A>G (p.Thr159=)
n.747A>G
n.737A>G
 ClinVar
2g.47412443A>TCA425967405MSH2c.675A>T (p.Thr225=)
c.477A>T (p.Thr159=)
n.747A>T
n.737A>T
2g.47412443_47412447delinsTAATCA021733MSH2c.675_679delinsTAAT (p.Glu226AsnfsTer20)
c.477_481delinsTAAT (p.Glu160AsnfsTer20)
n.747_751delinsTAAT
n.737_741delinsTAAT
 ClinVar dbSNP
2g.47412448_47412451delCA021730MSH2c.680_683del (p.Arg227LysfsTer18)
c.482_485del (p.Arg161LysfsTer18)
n.752_755del
n.742_745del
 ClinVar dbSNP
2g.47412444G>ACA346731814MSH2c.676G>A (p.Glu226Lys)
c.478G>A (p.Glu160Lys)
n.748G>A
n.738G>A
 ClinVar dbSNP
2g.47412444G>CCA346731817MSH2c.676G>C (p.Glu226Gln)
c.478G>C (p.Glu160Gln)
n.748G>C
n.738G>C
 dbSNP
2g.47412444G>TCA346731820MSH2c.676G>T (p.Glu226Ter)
c.478G>T (p.Glu160Ter)
n.748G>T
n.738G>T
 ClinVar
2g.47412444_47412445delinsGACA2495832691MSH2c.676_677delinsGA (p.Glu226=)
c.478_479delinsGA (p.Glu160=)
n.748_749delinsGA
n.738_739delinsGA
2g.47412445A=CA2495832692MSH2c.677A= (p.Glu226=)
c.479A= (p.Glu160=)
n.749A=
n.739A=
2g.47412445A>CCA346731824MSH2c.677A>C (p.Glu226Ala)
c.479A>C (p.Glu160Ala)
n.749A>C
n.739A>C
2g.47412445A>GCA346731826MSH2c.677A>G (p.Glu226Gly)
c.479A>G (p.Glu160Gly)
n.749A>G
n.739A>G
 ClinVar dbSNP
2g.47412445A>TCA346731828MSH2c.677A>T (p.Glu226Val)
c.479A>T (p.Glu160Val)
n.749A>T
n.739A>T
2g.47412447dupCA2586969192MSH2c.679dup (p.Arg227LysfsTer5)
c.481dup (p.Arg161LysfsTer5)
n.751dup
n.741dup
2g.47412447delCA915943887MSH2c.679del (p.Arg227GlufsTer19)
c.481del (p.Arg161GlufsTer19)
n.751del
n.741del
 ClinVar dbSNP
2g.47412446A>CCA346731832MSH2c.678A>C (p.Glu226Asp)
c.480A>C (p.Glu160Asp)
n.750A>C
n.740A>C
2g.47412446A>GCA425967425MSH2c.678A>G (p.Glu226=)
c.480A>G (p.Glu160=)
n.750A>G
n.740A>G
2g.47412446A>TCA346731835MSH2c.678A>T (p.Glu226Asp)
c.480A>T (p.Glu160Asp)
n.750A>T
n.740A>T
 dbSNP
2g.47412446_47412448delinsAAGCA2495832693MSH2c.678_680delinsAAG (p.Glu226=)
c.480_482delinsAAG (p.Glu160=)
n.750_752delinsAAG
n.740_742delinsAAG
2g.47412447A=CA2495832694MSH2c.679A= (p.Arg227=)
c.481A= (p.Arg161=)
n.751A=
n.741A=
2g.47412447A>CCA425967429MSH2c.679A>C (p.Arg227=)
c.481A>C (p.Arg161=)
n.751A>C
n.741A>C
2g.47412447A>GCA040008MSH2c.679A>G (p.Arg227Gly)
c.481A>G (p.Arg161Gly)
n.751A>G
n.741A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412447A>TCA346731838MSH2c.679A>T (p.Arg227Ter)
c.481A>T (p.Arg161Ter)
n.751A>T
n.741A>T
 ClinVar
2g.47412448_47412449delCA913187974MSH2c.680_681del (p.Arg227LysfsTer4)
c.482_483del (p.Arg161LysfsTer4)
n.752_753del
n.742_743del
 ClinVar dbSNP
2g.47412448delCA2580066636MSH2c.680del (p.Arg227LysfsTer19)
c.482del (p.Arg161LysfsTer19)
n.752del
n.742del
 ClinVar
2g.47412448G>ACA346731845MSH2c.680G>A (p.Arg227Lys)
c.482G>A (p.Arg161Lys)
n.752G>A
n.742G>A
 ClinVar
2g.47412448G>CCA346731847MSH2c.680G>C (p.Arg227Thr)
c.482G>C (p.Arg161Thr)
n.752G>C
n.742G>C
2g.47412448G>TCA346731849MSH2c.680G>T (p.Arg227Ile)
c.482G>T (p.Arg161Ile)
n.752G>T
n.742G>T
 ClinVar
2g.47412448dupCA2580612945MSH2c.680dup (p.Ala230SerfsTer2)
c.482dup (p.Ala164SerfsTer2)
n.752dup
n.742dup
 ClinVar
2g.47412448_47412450delinsGAACA2495832695MSH2c.680_682delinsGAA (p.Arg227=)
c.482_484delinsGAA (p.Arg161=)
n.752_754delinsGAA
n.742_744delinsGAA
2g.47412449A=CA2495832696MSH2c.681A= (p.Arg227=)
c.483A= (p.Arg161=)
n.753A=
n.743A=
2g.47412449A>CCA10577944MSH2c.681A>C (p.Arg227Ser)
c.483A>C (p.Arg161Ser)
n.753A>C
n.743A>C
 ClinVar dbSNP
2g.47412449A>GCA425967445MSH2c.681A>G (p.Arg227=)
c.483A>G (p.Arg161=)
n.753A>G
n.743A>G
2g.47412449A>TCA346731861MSH2c.681A>T (p.Arg227Ser)
c.483A>T (p.Arg161Ser)
n.753A>T
n.743A>T
 ClinVar dbSNP
2g.47412449_47412450delinsCCA2580066862MSH2c.681_682delinsC (p.Arg227SerfsTer19)
c.483_484delinsC (p.Arg161SerfsTer19)
n.753_754delinsC
n.743_744delinsC
 ClinVar
2g.47412455dupCA021991MSH2c.687dup (p.Ala230SerfsTer2)
c.489dup (p.Ala164SerfsTer2)
n.759dup
n.749dup
 ClinVar dbSNP gnomAD v4
2g.47412455delCA021998MSH2c.687del (p.Ala230LeufsTer16)
c.489del (p.Ala164LeufsTer16)
n.759del
n.749del
 ClinVar dbSNP gnomAD v4 COSMIC
2g.47412454_47412455delCA021960MSH2c.686_687del (p.Lys229SerfsTer2)
c.488_489del (p.Lys163SerfsTer2)
n.758_759del
n.748_749del
 ClinVar dbSNP
2g.47412452_47412455delCA2580066865MSH2c.684_687del (p.Lys229LeufsTer16)
c.486_489del (p.Lys163LeufsTer16)
n.756_759del
n.746_749del
 ClinVar
2g.47412449_47412457delinsGAAAAAGGCA2580066864MSH2c.681_689delinsGAAAAAGG (p.Ala230ValfsTer16)
c.483_491delinsGAAAAAGG (p.Ala164ValfsTer16)
n.753_761delinsGAAAAAGG
n.743_751delinsGAAAAAGG
 ClinVar
2g.47412450A=CA2495832697MSH2c.682A= (p.Lys228=)
c.484A= (p.Lys162=)
n.754A=
n.744A=
2g.47412450A>CCA346731864MSH2c.682A>C (p.Lys228Gln)
c.484A>C (p.Lys162Gln)
n.754A>C
n.744A>C
 gnomAD v4
2g.47412450A>GCA040044MSH2c.682A>G (p.Lys228Glu)
c.484A>G (p.Lys162Glu)
n.754A>G
n.744A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412450A>TCA346731867MSH2c.682A>T (p.Lys228Ter)
c.484A>T (p.Lys162Ter)
n.754A>T
n.744A>T
 dbSNP
2g.47412451A>CCA346731874MSH2c.683A>C (p.Lys228Thr)
c.485A>C (p.Lys162Thr)
n.755A>C
n.745A>C
2g.47412451A>GCA346731875MSH2c.683A>G (p.Lys228Arg)
c.485A>G (p.Lys162Arg)
n.755A>G
n.745A>G
2g.47412451A>TCA346731871MSH2c.683A>T (p.Lys228Ile)
c.485A>T (p.Lys162Ile)
n.755A>T
n.745A>T
2g.47412452A>CCA346731876MSH2c.684A>C (p.Lys228Asn)
c.486A>C (p.Lys162Asn)
n.756A>C
n.746A>C
2g.47412452A>GCA425967472MSH2c.684A>G (p.Lys228=)
c.486A>G (p.Lys162=)
n.756A>G
n.746A>G
2g.47412452A>TCA346731877MSH2c.684A>T (p.Lys228Asn)
c.486A>T (p.Lys162Asn)
n.756A>T
n.746A>T
 dbSNP
2g.47412453A=CA2495832698MSH2c.685A= (p.Lys229=)
c.487A= (p.Lys163=)
n.757A=
n.747A=
2g.47412453A>CCA346731878MSH2c.685A>C (p.Lys229Gln)
c.487A>C (p.Lys163Gln)
n.757A>C
n.747A>C
2g.47412453A>GCA346731880MSH2c.685A>G (p.Lys229Glu)
c.487A>G (p.Lys163Glu)
n.757A>G
n.747A>G
2g.47412453A>TCA021947MSH2c.685A>T (p.Lys229Ter)
c.487A>T (p.Lys163Ter)
n.757A>T
n.747A>T
 ClinVar dbSNP
2g.47412454A>CCA346731887MSH2c.686A>C (p.Lys229Thr)
c.488A>C (p.Lys163Thr)
n.758A>C
n.748A>C
2g.47412454A>GCA346731886MSH2c.686A>G (p.Lys229Arg)
c.488A>G (p.Lys163Arg)
n.758A>G
n.748A>G
2g.47412454A>TCA346731884MSH2c.686A>T (p.Lys229Ile)
c.488A>T (p.Lys163Ile)
n.758A>T
n.748A>T
 ClinVar dbSNP
2g.47412454_47412455insTGAAAATTATAACATTGATAACTATCA2699268402MSH2c.686_687insTGAAAATTATAACATTGATAACTAT (p.Lys229AsnfsTer11)
c.488_489insTGAAAATTATAACATTGATAACTAT (p.Lys163AsnfsTer11)
n.758_759insTGAAAATTATAACATTGATAACTAT
n.748_749insTGAAAATTATAACATTGATAACTAT
 dbSNP
2g.47412455A=CA2495832699MSH2c.687A= (p.Lys229=)
c.489A= (p.Lys163=)
n.759A=
n.749A=
2g.47412455A>CCA346731890MSH2c.687A>C (p.Lys229Asn)
c.489A>C (p.Lys163Asn)
n.759A>C
n.749A>C
2g.47412455A>GCA425967492MSH2c.687A>G (p.Lys229=)
c.489A>G (p.Lys163=)
n.759A>G
n.749A>G
 ClinVar gnomAD v4
2g.47412455A>TCA346731892MSH2c.687A>T (p.Lys229Asn)
c.489A>T (p.Lys163Asn)
n.759A>T
n.749A>T
 gnomAD v4
2g.47412455_47412456insTCA645369190MSH2c.687_688insT (p.Ala230CysfsTer2)
c.489_490insT (p.Ala164CysfsTer2)
n.759_760insT
n.749_750insT
 ClinVar dbSNP
2g.47412456G>ACA346731895MSH2c.688G>A (p.Ala230Thr)
c.490G>A (p.Ala164Thr)
n.760G>A
n.750G>A
 ClinVar dbSNP gnomAD v4
2g.47412456G>CCA346731898MSH2c.688G>C (p.Ala230Pro)
c.490G>C (p.Ala164Pro)
n.760G>C
n.750G>C
 ClinVar dbSNP
2g.47412456G=CA2495832700MSH2c.688G= (p.Ala230=)
c.490G= (p.Ala164=)
n.760G=
n.750G=
2g.47412456G>TCA346731899MSH2c.688G>T (p.Ala230Ser)
c.490G>T (p.Ala164Ser)
n.760G>T
n.750G>T
 ClinVar dbSNP
2g.47412457delCA2580066872MSH2c.689del (p.Ala230ValfsTer16)
c.491del (p.Ala164ValfsTer16)
n.761del
n.751del
 ClinVar
2g.47412457C>ACA346731907MSH2c.689C>A (p.Ala230Asp)
c.491C>A (p.Ala164Asp)
n.761C>A
n.751C>A
 ClinVar dbSNP gnomAD v4
2g.47412457C=CA2495832701MSH2c.689C= (p.Ala230=)
c.491C= (p.Ala164=)
n.761C=
n.751C=
2g.47412457C>GCA346731904MSH2c.689C>G (p.Ala230Gly)
c.491C>G (p.Ala164Gly)
n.761C>G
n.751C>G
 ClinVar dbSNP
2g.47412457C>TCA346731902MSH2c.689C>T (p.Ala230Val)
c.491C>T (p.Ala164Val)
n.761C>T
n.751C>T
 ClinVar dbSNP gnomAD v4
2g.47412457_47412459delinsTTCA2586969194MSH2c.689_691delinsTT (p.Ala230ValfsTer16)
c.491_493delinsTT (p.Ala164ValfsTer16)
n.761_763delinsTT
n.751_753delinsTT
2g.47412458T>ACA425967509MSH2c.690T>A (p.Ala230=)
c.492T>A (p.Ala164=)
n.762T>A
n.752T>A
 dbSNP
2g.47412458T>CCA425967512MSH2c.690T>C (p.Ala230=)
c.492T>C (p.Ala164=)
n.762T>C
n.752T>C
 ClinVar dbSNP gnomAD v4 COSMIC
2g.47412458T>GCA425967506MSH2c.690T>G (p.Ala230=)
c.492T>G (p.Ala164=)
n.762T>G
n.752T>G
2g.47412458T=CA2495832703MSH2c.690T= (p.Ala230=)
c.492T= (p.Ala164=)
n.762T=
n.752T=
2g.47412458_47412459delinsTGCA2495832702MSH2c.690_691delinsTG (p.Ala230=)
c.492_493delinsTG (p.Ala164=)
n.762_763delinsTG
n.752_753delinsTG
2g.47412458_47412460delCA2697548109MSH2c.690_692del (p.Asp231del)
c.492_494del (p.Asp165del)
n.762_764del
n.752_754del
 ClinVar
2g.47412459delCA022028MSH2c.691del (p.Asp231ThrfsTer15)
c.493del (p.Asp165ThrfsTer15)
n.763del
n.753del
 ClinVar dbSNP
2g.47412459G>ACA346731911MSH2c.691G>A (p.Asp231Asn)
c.493G>A (p.Asp165Asn)
n.763G>A
n.753G>A
 ClinVar dbSNP gnomAD v4
2g.47412459G>CCA346731914MSH2c.691G>C (p.Asp231His)
c.493G>C (p.Asp165His)
n.763G>C
n.753G>C
 dbSNP gnomAD v3 gnomAD v4
2g.47412459G=CA2495832704MSH2c.691G= (p.Asp231=)
c.493G= (p.Asp165=)
n.763G=
n.753G=
2g.47412459G>TCA346731917MSH2c.691G>T (p.Asp231Tyr)
c.493G>T (p.Asp165Tyr)
n.763G>T
n.753G>T
 ClinVar dbSNP gnomAD v4
2g.47412460A>CCA346731928MSH2c.692A>C (p.Asp231Ala)
c.494A>C (p.Asp165Ala)
n.764A>C
n.754A>C
2g.47412460A>GCA346731930MSH2c.692A>G (p.Asp231Gly)
c.494A>G (p.Asp165Gly)
n.764A>G
n.754A>G
 gnomAD v4
2g.47412460A>TCA346731932MSH2c.692A>T (p.Asp231Val)
c.494A>T (p.Asp165Val)
n.764A>T
n.754A>T
 dbSNP
2g.47412461C>ACA346731937MSH2c.693C>A (p.Asp231Glu)
c.495C>A (p.Asp165Glu)
n.765C>A
n.755C>A
2g.47412461C=CA2495832706MSH2c.693C= (p.Asp231=)
c.495C= (p.Asp165=)
n.765C=
n.755C=
2g.47412461C>GCA346731939MSH2c.693C>G (p.Asp231Glu)
c.495C>G (p.Asp165Glu)
n.765C>G
n.755C>G
 dbSNP
2g.47412461C>TCA040060MSH2c.693C>T (p.Asp231=)
c.495C>T (p.Asp165=)
n.765C>T
n.755C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412461_47412463delinsCTTCA2495832705MSH2c.693_695delinsCTT (p.Asp231=)
c.495_497delinsCTT (p.Asp165=)
n.765_767delinsCTT
n.755_757delinsCTT
2g.47412462T>ACA346731946MSH2c.694T>A (p.Phe232Ile)
c.496T>A (p.Phe166Ile)
n.766T>A
n.756T>A
2g.47412462T>CCA346731951MSH2c.694T>C (p.Phe232Leu)
c.496T>C (p.Phe166Leu)
n.766T>C
n.756T>C
2g.47412462T>GCA346731949MSH2c.694T>G (p.Phe232Val)
c.496T>G (p.Phe166Val)
n.766T>G
n.756T>G
2g.47412465dupCA2697548110MSH2c.697dup (p.Ser233PhefsTer23)
c.499dup (p.Ser167PhefsTer23)
n.769dup
n.759dup
 ClinVar
2g.47412465delCA2499215990MSH2c.697del (p.Ser233ProfsTer13)
c.499del (p.Ser167ProfsTer13)
n.769del
n.759del
 ClinVar dbSNP
2g.47412464_47412465delCA022033MSH2c.696_697del (p.Ser233HisfsTer22)
c.498_499del (p.Ser167HisfsTer22)
n.768_769del
n.758_759del
 ClinVar dbSNP
2g.47412463T>ACA346731955MSH2c.695T>A (p.Phe232Tyr)
c.497T>A (p.Phe166Tyr)
n.767T>A
n.757T>A
2g.47412463T>CCA346731957MSH2c.695T>C (p.Phe232Ser)
c.497T>C (p.Phe166Ser)
n.767T>C
n.757T>C
 dbSNP gnomAD v4
2g.47412463T>GCA346731961MSH2c.695T>G (p.Phe232Cys)
c.497T>G (p.Phe166Cys)
n.767T>G
n.757T>G
2g.47412464T>ACA346731964MSH2c.696T>A (p.Phe232Leu)
c.498T>A (p.Phe166Leu)
n.768T>A
n.758T>A
2g.47412464T>CCA425967560MSH2c.696T>C (p.Phe232=)
c.498T>C (p.Phe166=)
n.768T>C
n.758T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412464T>GCA346731966MSH2c.696T>G (p.Phe232Leu)
c.498T>G (p.Phe166Leu)
n.768T>G
n.758T>G
2g.47412464T=CA2495832707MSH2c.696T= (p.Phe232=)
c.498T= (p.Phe166=)
n.768T=
n.758T=
2g.47412465T>ACA346731976MSH2c.697T>A (p.Ser233Thr)
c.499T>A (p.Ser167Thr)
n.769T>A
n.759T>A
2g.47412465T>CCA346731973MSH2c.697T>C (p.Ser233Pro)
c.499T>C (p.Ser167Pro)
n.769T>C
n.759T>C
 gnomAD v4
2g.47412465T>GCA346731969MSH2c.697T>G (p.Ser233Ala)
c.499T>G (p.Ser167Ala)
n.769T>G
n.759T>G
2g.47412466C>ACA346731980MSH2c.698C>A (p.Ser233Tyr)
c.500C>A (p.Ser167Tyr)
n.770C>A
n.760C>A
 dbSNP
2g.47412466C=CA2495832708MSH2c.698C= (p.Ser233=)
c.500C= (p.Ser167=)
n.770C=
n.760C=
2g.47412466C>GCA022041MSH2c.698C>G (p.Ser233Cys)
c.500C>G (p.Ser167Cys)
n.770C>G
n.760C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412466C>TCA346731983MSH2c.698C>T (p.Ser233Phe)
c.500C>T (p.Ser167Phe)
n.770C>T
n.760C>T
 ClinVar dbSNP gnomAD v4
2g.47412467delCA1139771116MSH2c.699del (p.Thr234GlnfsTer12)
c.501del (p.Thr168GlnfsTer12)
n.771del
n.761del
 ClinVar
2g.47412466_47412484delinsCCACAAAAGACATTTATCACA2495832709MSH2c.698_716delinsCCACAAAAGACATTTATCA (p.Ser233=)
c.500_518delinsCCACAAAAGACATTTATCA (p.Ser167=)
n.770_788delinsCCACAAAAGACATTTATCA
n.760_778delinsCCACAAAAGACATTTATCA
2g.47412467C>ACA425967576MSH2c.699C>A (p.Ser233=)
c.501C>A (p.Ser167=)
n.771C>A
n.761C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412467C=CA2495832711MSH2c.699C= (p.Ser233=)
c.501C= (p.Ser167=)
n.771C=
n.761C=
2g.47412467C>GCA425967578MSH2c.699C>G (p.Ser233=)
c.501C>G (p.Ser167=)
n.771C>G
n.761C>G
2g.47412467C>TCA425967581MSH2c.699C>T (p.Ser233=)
c.501C>T (p.Ser167=)
n.771C>T
n.761C>T
 dbSNP gnomAD v4 COSMIC
2g.47412467_47412484delCA2495832710MSH2c.699_716del (p.Thr234_Gln239del)
c.501_518del (p.Thr168_Gln173del)
n.771_788del
n.761_778del
 ClinVar dbSNP
2g.47412468A=CA2495832712MSH2c.700A= (p.Thr234=)
c.502A= (p.Thr168=)
n.772A=
n.762A=
2g.47412468A>CCA346731984MSH2c.700A>C (p.Thr234Pro)
c.502A>C (p.Thr168Pro)
n.772A>C
n.762A>C
2g.47412468A>GCA346731985MSH2c.700A>G (p.Thr234Ala)
c.502A>G (p.Thr168Ala)
n.772A>G
n.762A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412468A>TCA346731986MSH2c.700A>T (p.Thr234Ser)
c.502A>T (p.Thr168Ser)
n.772A>T
n.762A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412471_47412477delCA2499215991MSH2c.703_709del (p.Lys235PhefsTer9)
c.505_511del (p.Lys169PhefsTer9)
n.775_781del
n.765_771del
 ClinVar dbSNP
2g.47412469C>ACA346731989MSH2c.701C>A (p.Thr234Lys)
c.503C>A (p.Thr168Lys)
n.773C>A
n.763C>A
 ClinVar
2g.47412469C=CA2495832714MSH2c.701C= (p.Thr234=)
c.503C= (p.Thr168=)
n.773C=
n.763C=
2g.47412469C>GCA10577945MSH2c.701C>G (p.Thr234Arg)
c.503C>G (p.Thr168Arg)
n.773C>G
n.763C>G
 ClinVar dbSNP
2g.47412469C>TCA022053MSH2c.701C>T (p.Thr234Ile)
c.503C>T (p.Thr168Ile)
n.773C>T
n.763C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412469_47412471delinsCAACA2495832713MSH2c.701_703delinsCAA (p.Thr234=)
c.503_505delinsCAA (p.Thr168=)
n.773_775delinsCAA
n.763_765delinsCAA
2g.47412470A=CA2495832715MSH2c.702A= (p.Thr234=)
c.504A= (p.Thr168=)
n.774A=
n.764A=
2g.47412470A>CCA425967595MSH2c.702A>C (p.Thr234=)
c.504A>C (p.Thr168=)
n.774A>C
n.764A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412470A>GCA040148MSH2c.702A>G (p.Thr234=)
c.504A>G (p.Thr168=)
n.774A>G
n.764A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412470A>TCA425967599MSH2c.702A>T (p.Thr234=)
c.504A>T (p.Thr168=)
n.774A>T
n.764A>T
 gnomAD v4
2g.47412473delCA022063MSH2c.705del (p.Asp236ThrfsTer10)
c.507del (p.Asp170ThrfsTer10)
n.777del
n.767del
 ClinVar dbSNP
2g.47412472_47412473delCA022059MSH2c.704_705del (p.Lys235ArgfsTer20)
c.506_507del (p.Lys169ArgfsTer20)
n.776_777del
n.766_767del
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412471A=CA2495832716MSH2c.703A= (p.Lys235=)
c.505A= (p.Lys169=)
n.775A=
n.765A=
2g.47412471A>CCA346732005MSH2c.703A>C (p.Lys235Gln)
c.505A>C (p.Lys169Gln)
n.775A>C
n.765A>C
2g.47412471A>GCA040162MSH2c.703A>G (p.Lys235Glu)
c.505A>G (p.Lys169Glu)
n.775A>G
n.765A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412471A>TCA346732002MSH2c.703A>T (p.Lys235Ter)
c.505A>T (p.Lys169Ter)
n.775A>T
n.765A>T
2g.47412472A>CCA346732011MSH2c.704A>C (p.Lys235Thr)
c.506A>C (p.Lys169Thr)
n.776A>C
n.766A>C
 ClinVar dbSNP
2g.47412472A>GCA346732013MSH2c.704A>G (p.Lys235Arg)
c.506A>G (p.Lys169Arg)
n.776A>G
n.766A>G
2g.47412472A>TCA346732017MSH2c.704A>T (p.Lys235Ile)
c.506A>T (p.Lys169Ile)
n.776A>T
n.766A>T
2g.47412473A>CCA346732020MSH2c.705A>C (p.Lys235Asn)
c.507A>C (p.Lys169Asn)
n.777A>C
n.767A>C
2g.47412473A>GCA425967624MSH2c.705A>G (p.Lys235=)
c.507A>G (p.Lys169=)
n.777A>G
n.767A>G
2g.47412473A>TCA346732023MSH2c.705A>T (p.Lys235Asn)
c.507A>T (p.Lys169Asn)
n.777A>T
n.767A>T
 dbSNP

Number of alleles fetched