| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.80674935_80674956del | CA2578350228 | MSH3 | c.1028-48_1028-27del (n.1028-48_1028-27del) c.860-48_860-27del (n.860-48_860-27del) | |
| 5 | g.80674937G>A | CA560552886 | MSH3 | c.1028-46G>A (n.1028-46G>A) c.860-46G>A (n.860-46G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674937G= | CA1558493056 | MSH3 | c.1028-46G= (n.1028-46G=) c.860-46G= (n.860-46G=) | |
| 5 | g.80674938G>A | CA2709328675 | MSH3 | c.1028-45G>A (n.1028-45G>A) c.860-45G>A (n.860-45G>A) | dbSNP |
| 5 | g.80674939A>G | CA2674442928 | MSH3 | c.1028-44A>G (n.1028-44A>G) c.860-44A>G (n.860-44A>G) | gnomAD v4 |
| 5 | g.80674943A>G | CA2674442929 | MSH3 | c.1028-40A>G (n.1028-40A>G) c.860-40A>G (n.860-40A>G) | gnomAD v4 |
| 5 | g.80674944G>A | CA2674442930 | MSH3 | c.1028-39G>A (n.1028-39G>A) c.860-39G>A (n.860-39G>A) | gnomAD v4 |
| 5 | g.80674945A= | CA1558493061 | MSH3 | c.1028-38A= (n.1028-38A=) c.860-38A= (n.860-38A=) | |
| 5 | g.80674945A>C | CA121295093 | MSH3 | c.1028-38A>C (n.1028-38A>C) c.860-38A>C (n.860-38A>C) | dbSNP gnomAD v4 |
| 5 | g.80674945A>G | CA3327777 | MSH3 | c.1028-38A>G (n.1028-38A>G) c.860-38A>G (n.860-38A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674946A>G | CA2709328712 | MSH3 | c.1028-37A>G (n.1028-37A>G) c.860-37A>G (n.860-37A>G) | dbSNP |
| 5 | g.80674947T>A | CA560552887 | MSH3 | c.1028-36T>A (n.1028-36T>A) c.860-36T>A (n.860-36T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80674947T>C | CA2674442931 | MSH3 | c.1028-36T>C (n.1028-36T>C) c.860-36T>C (n.860-36T>C) | gnomAD v4 |
| 5 | g.80674947T= | CA1558493065 | MSH3 | c.1028-36T= (n.1028-36T=) c.860-36T= (n.860-36T=) | |
| 5 | g.80674948T>G | CA2674442932 | MSH3 | c.1028-35T>G (n.1028-35T>G) c.860-35T>G (n.860-35T>G) | gnomAD v4 |
| 5 | g.80674950A>G | CA2674442933 | MSH3 | c.1028-33A>G (n.1028-33A>G) c.860-33A>G (n.860-33A>G) | gnomAD v4 |
| 5 | g.80674951G>A | CA560552889 | MSH3 | c.1028-32G>A (n.1028-32G>A) c.860-32G>A (n.860-32G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80674951G= | CA1558493066 | MSH3 | c.1028-32G= (n.1028-32G=) c.860-32G= (n.860-32G=) | |
| 5 | g.80674952C>A | CA121295100 | MSH3 | c.1028-31C>A (n.1028-31C>A) c.860-31C>A (n.860-31C>A) | dbSNP gnomAD v4 |
| 5 | g.80674952C= | CA1558493069 | MSH3 | c.1028-31C= (n.1028-31C=) c.860-31C= (n.860-31C=) | |
| 5 | g.80674952C>G | CA1077958985 | MSH3 | c.1028-31C>G (n.1028-31C>G) c.860-31C>G (n.860-31C>G) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674952C>T | CA2578350231 | MSH3 | c.1028-31C>T (n.1028-31C>T) c.860-31C>T (n.860-31C>T) | |
| 5 | g.80674953A= | CA1558493072 | MSH3 | c.1028-30A= (n.1028-30A=) c.860-30A= (n.860-30A=) | |
| 5 | g.80674953A>G | CA3327778 | MSH3 | c.1028-30A>G (n.1028-30A>G) c.860-30A>G (n.860-30A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80674955A= | CA1558493074 | MSH3 | c.1028-28A= (n.1028-28A=) c.860-28A= (n.860-28A=) | |
| 5 | g.80674955A>G | CA814453642 | MSH3 | c.1028-28A>G (n.1028-28A>G) c.860-28A>G (n.860-28A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674956T>C | CA3327779 | MSH3 | c.1028-27T>C (n.1028-27T>C) c.860-27T>C (n.860-27T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674956T= | CA1558493077 | MSH3 | c.1028-27T= (n.1028-27T=) c.860-27T= (n.860-27T=) | |
| 5 | g.80674958_80674961del | CA2674442938 | MSH3 | c.1028-25_1028-22del (n.1028-25_1028-22del) c.860-25_860-22del (n.860-25_860-22del) | gnomAD v4 |
| 5 | g.80674957A>G | CA2674442939 | MSH3 | c.1028-26A>G (n.1028-26A>G) c.860-26A>G (n.860-26A>G) | gnomAD v4 |
| 5 | g.80674957A>T | CA2674442940 | MSH3 | c.1028-26A>T (n.1028-26A>T) c.860-26A>T (n.860-26A>T) | gnomAD v4 |
| 5 | g.80674958A= | CA1558493080 | MSH3 | c.1028-25A= (n.1028-25A=) c.860-25A= (n.860-25A=) | |
| 5 | g.80674958A>G | CA560552896 | MSH3 | c.1028-25A>G (n.1028-25A>G) c.860-25A>G (n.860-25A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674961_80674963del | CA2578350232 | MSH3 | c.1028-22_1028-20del (n.1028-22_1028-20del) c.860-22_860-20del (n.860-22_860-20del) | gnomAD v4 |
| 5 | g.80674961A>G | CA2674442942 | MSH3 | c.1028-22A>G (n.1028-22A>G) c.860-22A>G (n.860-22A>G) | gnomAD v4 |
| 5 | g.80674966T>A | CA2573139910 | MSH3 | c.1028-17T>A (n.1028-17T>A) c.860-17T>A (n.860-17T>A) | ClinVar dbSNP |
| 5 | g.80674966T>C | CA1558493085 | MSH3 | c.1028-17T>C (n.1028-17T>C) c.860-17T>C (n.860-17T>C) | dbSNP gnomAD v4 |
| 5 | g.80674966T= | CA1558493083 | MSH3 | c.1028-17T= (n.1028-17T=) c.860-17T= (n.860-17T=) | |
| 5 | g.80674967C>A | CA2573139913 | MSH3 | c.1028-16C>A (n.1028-16C>A) c.860-16C>A (n.860-16C>A) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674967C>G | CA2580073603 | MSH3 | c.1028-16C>G (n.1028-16C>G) c.860-16C>G (n.860-16C>G) | ClinVar gnomAD v4 |
| 5 | g.80674967dup | CA2740091761 | MSH3 | c.1028-16dup (n.1028-16dup) c.860-16dup (n.860-16dup) | ClinVar |
| 5 | g.80674969T>G | CA121295105 | MSH3 | c.1028-14T>G (n.1028-14T>G) c.860-14T>G (n.860-14T>G) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674969T= | CA1558493087 | MSH3 | c.1028-14T= (n.1028-14T=) c.860-14T= (n.860-14T=) | |
| 5 | g.80674972_80674975del | CA2600112703 | MSH3 | c.1028-11_1028-8del (n.1028-11_1028-8del) c.860-11_860-8del (n.860-11_860-8del) | ClinVar gnomAD v3 gnomAD v4 |
| 5 | g.80674971A= | CA1558493090 | MSH3 | c.1028-12A= (n.1028-12A=) c.860-12A= (n.860-12A=) | |
| 5 | g.80674971A>G | CA2674442951 | MSH3 | c.1028-12A>G (n.1028-12A>G) c.860-12A>G (n.860-12A>G) | gnomAD v4 |
| 5 | g.80674971A>T | CA560552899 | MSH3 | c.1028-12A>T (n.1028-12A>T) c.860-12A>T (n.860-12A>T) | dbSNP gnomAD v2 |
| 5 | g.80674972A= | CA1558493092 | MSH3 | c.1028-11A= (n.1028-11A=) c.860-11A= (n.860-11A=) | |
| 5 | g.80674972A>C | CA2513826450 | MSH3 | c.1028-11A>C (n.1028-11A>C) c.860-11A>C (n.860-11A>C) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674972A>T | CA814453654 | MSH3 | c.1028-11A>T (n.1028-11A>T) c.860-11A>T (n.860-11A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674979_80674981del | CA2580613580 | MSH3 | c.1028-4_1028-2del (n.1028-4_1028-2del) c.860-4_860-2del (n.860-4_860-2del) | ClinVar dbSNP |
| 5 | g.80674973T>G | CA916082722 | MSH3 | c.1028-10T>G (n.1028-10T>G) c.860-10T>G (n.860-10T>G) | ClinVar dbSNP |
| 5 | g.80674973T= | CA1558493097 | MSH3 | c.1028-10T= (n.1028-10T=) c.860-10T= (n.860-10T=) | |
| 5 | g.80674974T>C | CA2740091762 | MSH3 | c.1028-9T>C (n.1028-9T>C) c.860-9T>C (n.860-9T>C) | ClinVar |
| 5 | g.80674975A>G | CA2573139914 | MSH3 | c.1028-8A>G (n.1028-8A>G) c.860-8A>G (n.860-8A>G) | ClinVar dbSNP |
| 5 | g.80674977T>C | CA3327780 | MSH3 | c.1028-6T>C (n.1028-6T>C) c.860-6T>C (n.860-6T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80674977T= | CA1558493101 | MSH3 | c.1028-6T= (n.1028-6T=) c.860-6T= (n.860-6T=) | |
| 5 | g.80674978A= | CA1558493113 | MSH3 | c.1028-5A= (n.1028-5A=) c.860-5A= (n.860-5A=) | |
| 5 | g.80674978A>G | CA3327782 | MSH3 | c.1028-5A>G (n.1028-5A>G) c.860-5A>G (n.860-5A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674978A>T | CA3327781 | MSH3 | c.1028-5A>T (n.1028-5A>T) c.860-5A>T (n.860-5A>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80674979T>C | CA814453661 | MSH3 | c.1028-4T>C (n.1028-4T>C) c.860-4T>C (n.860-4T>C) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674979T= | CA1558493122 | MSH3 | c.1028-4T= (n.1028-4T=) c.860-4T= (n.860-4T=) | |
| 5 | g.80674981A= | CA1558493129 | MSH3 | c.1028-2A= (n.1028-2A=) c.860-2A= (n.860-2A=) | |
| 5 | g.80674981A>C | CA360267799 | MSH3 | c.1028-2A>C (n.1028-2A>C) c.860-2A>C (n.860-2A>C) | |
| 5 | g.80674981A>G | CA360267801 | MSH3 | c.1028-2A>G (n.1028-2A>G) c.860-2A>G (n.860-2A>G) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 5 | g.80674981A>T | CA360267803 | MSH3 | c.1028-2A>T (n.1028-2A>T) c.860-2A>T (n.860-2A>T) | ClinVar dbSNP |
| 5 | g.80674982A= | CA1558493137 | MSH3 | c.1028-1A= (n.1028-1A=) c.860-1A= (n.860-1A=) | |
| 5 | g.80674982A>C | CA360267805 | MSH3 | c.1028-1A>C (n.1028-1A>C) c.860-1A>C (n.860-1A>C) | ClinVar gnomAD v4 |
| 5 | g.80674982A>G | CA360267807 | MSH3 | c.1028-1A>G (n.1028-1A>G) c.860-1A>G (n.860-1A>G) | |
| 5 | g.80674982A>T | CA121295111 | MSH3 | c.1028-1A>T (n.1028-1A>T) c.860-1A>T (n.860-1A>T) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674983A= | CA1558493141 | MSH3 | c.1028A= (p.Asp343=) c.860A= (p.Asp287=) | |
| 5 | g.80674983A>C | CA360267810 | MSH3 | c.1028A>C (p.Asp343Ala) c.860A>C (p.Asp287Ala) | |
| 5 | g.80674983A>G | CA360267813 | MSH3 | c.1028A>G (p.Asp343Gly) c.860A>G (p.Asp287Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80674983A>T | CA360267811 | MSH3 | c.1028A>T (p.Asp343Val) c.860A>T (p.Asp287Val) | |
| 5 | g.80674984T>A | CA360267814 | MSH3 | c.1029T>A (p.Asp343Glu) c.861T>A (p.Asp287Glu) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674984T>C | CA445159583 | MSH3 | c.1029T>C (p.Asp343=) c.861T>C (p.Asp287=) | ClinVar dbSNP |
| 5 | g.80674984T>G | CA360267815 | MSH3 | c.1029T>G (p.Asp343Glu) c.861T>G (p.Asp287Glu) | |
| 5 | g.80674985G>A | CA360267818 | MSH3 | c.1030G>A (p.Val344Met) c.862G>A (p.Val288Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674985G>C | CA360267819 | MSH3 | c.1030G>C (p.Val344Leu) c.862G>C (p.Val288Leu) | |
| 5 | g.80674985G= | CA1558493147 | MSH3 | c.1030G= (p.Val344=) c.862G= (p.Val288=) | |
| 5 | g.80674985G>T | CA360267821 | MSH3 | c.1030G>T (p.Val344Leu) c.862G>T (p.Val288Leu) | ClinVar |
| 5 | g.80674986T>A | CA360267823 | MSH3 | c.1031T>A (p.Val344Glu) c.863T>A (p.Val288Glu) | |
| 5 | g.80674986T>C | CA360267825 | MSH3 | c.1031T>C (p.Val344Ala) c.863T>C (p.Val288Ala) | |
| 5 | g.80674986T>G | CA360267826 | MSH3 | c.1031T>G (p.Val344Gly) c.863T>G (p.Val288Gly) | |
| 5 | g.80674987G>A | CA445159590 | MSH3 | c.1032G>A (p.Val344=) c.864G>A (p.Val288=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674987G>C | CA445159591 | MSH3 | c.1032G>C (p.Val344=) c.864G>C (p.Val288=) | |
| 5 | g.80674987G= | CA1558493157 | MSH3 | c.1032G= (p.Val344=) c.864G= (p.Val288=) | |
| 5 | g.80674987G>T | CA3327783 | MSH3 | c.1032G>T (p.Val344=) c.864G>T (p.Val288=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674988A>C | CA360267829 | MSH3 | c.1033A>C (p.Asn345His) c.865A>C (p.Asn289His) | |
| 5 | g.80674988A>G | CA360267831 | MSH3 | c.1033A>G (p.Asn345Asp) c.865A>G (p.Asn289Asp) | |
| 5 | g.80674988A>T | CA360267832 | MSH3 | c.1033A>T (p.Asn345Tyr) c.865A>T (p.Asn289Tyr) | ClinVar |
| 5 | g.80674989A= | CA1558493163 | MSH3 | c.1034A= (p.Asn345=) c.866A= (p.Asn289=) | |
| 5 | g.80674989A>C | CA360267838 | MSH3 | c.1034A>C (p.Asn345Thr) c.866A>C (p.Asn289Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674989A>G | CA360267837 | MSH3 | c.1034A>G (p.Asn345Ser) c.866A>G (p.Asn289Ser) | ClinVar dbSNP |
| 5 | g.80674989A>T | CA360267835 | MSH3 | c.1034A>T (p.Asn345Ile) c.866A>T (p.Asn289Ile) | |
| 5 | g.80674989_80674990delinsAT | CA1558493162 | MSH3 | c.1034_1035delinsAT (p.Asn345=) c.866_867delinsAT (p.Asn289=) | |
| 5 | g.80674990del | CA915943432 | MSH3 | c.1035del (p.Leu347Ter) c.867del (p.Leu291Ter) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674990T>A | CA360267841 | MSH3 | c.1035T>A (p.Asn345Lys) c.867T>A (p.Asn289Lys) | |
| 5 | g.80674990T>C | CA445159598 | MSH3 | c.1035T>C (p.Asn345=) c.867T>C (p.Asn289=) | |
| 5 | g.80674990T>G | CA360267842 | MSH3 | c.1035T>G (p.Asn345Lys) c.867T>G (p.Asn289Lys) | |
| 5 | g.80674991C>A | CA360267843 | MSH3 | c.1036C>A (p.Pro346Thr) c.868C>A (p.Pro290Thr) | dbSNP gnomAD v4 |
| 5 | g.80674991C= | CA1558493170 | MSH3 | c.1036C= (p.Pro346=) c.868C= (p.Pro290=) | |
| 5 | g.80674991C>G | CA360267845 | MSH3 | c.1036C>G (p.Pro346Ala) c.868C>G (p.Pro290Ala) | |
| 5 | g.80674991C>T | CA360267847 | MSH3 | c.1036C>T (p.Pro346Ser) c.868C>T (p.Pro290Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674992C>A | CA360267848 | MSH3 | c.1037C>A (p.Pro346His) c.869C>A (p.Pro290His) | COSMIC COSMIC |
| 5 | g.80674992C= | CA1558493178 | MSH3 | c.1037C= (p.Pro346=) c.869C= (p.Pro290=) | |
| 5 | g.80674992C>G | CA3327784 | MSH3 | c.1037C>G (p.Pro346Arg) c.869C>G (p.Pro290Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80674992C>T | CA360267850 | MSH3 | c.1037C>T (p.Pro346Leu) c.869C>T (p.Pro290Leu) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674993C>A | CA445159607 | MSH3 | c.1038C>A (p.Pro346=) c.870C>A (p.Pro290=) | |
| 5 | g.80674993C>G | CA445159609 | MSH3 | c.1038C>G (p.Pro346=) c.870C>G (p.Pro290=) | |
| 5 | g.80674993C>T | CA445159611 | MSH3 | c.1038C>T (p.Pro346=) c.870C>T (p.Pro290=) | gnomAD v4 |
| 5 | g.80674994C>A | CA360267852 | MSH3 | c.1039C>A (p.Leu347Ile) c.871C>A (p.Leu291Ile) | gnomAD v4 |
| 5 | g.80674994C= | CA1558493189 | MSH3 | c.1039C= (p.Leu347=) c.871C= (p.Leu291=) | |
| 5 | g.80674994C>G | CA360267854 | MSH3 | c.1039C>G (p.Leu347Val) c.871C>G (p.Leu291Val) | |
| 5 | g.80674994C>T | CA445159614 | MSH3 | c.1039C>T (p.Leu347=) c.871C>T (p.Leu291=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674994_80674995delinsCT | CA1558493190 | MSH3 | c.1039_1040delinsCT (p.Leu347=) c.871_872delinsCT (p.Leu291=) | |
| 5 | g.80674995del | CA915943433 | MSH3 | c.1040del (p.Leu347GlnfsTer8) c.872del (p.Leu291GlnfsTer8) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674995T>A | CA360267855 | MSH3 | c.1040T>A (p.Leu347Gln) c.872T>A (p.Leu291Gln) | |
| 5 | g.80674995T>C | CA360267858 | MSH3 | c.1040T>C (p.Leu347Pro) c.872T>C (p.Leu291Pro) | ClinVar gnomAD v4 |
| 5 | g.80674995T>G | CA360267860 | MSH3 | c.1040T>G (p.Leu347Arg) c.872T>G (p.Leu291Arg) | |
| 5 | g.80674996A= | CA1558493191 | MSH3 | c.1041A= (p.Leu347=) c.873A= (p.Leu291=) | |
| 5 | g.80674996A>C | CA445159618 | MSH3 | c.1041A>C (p.Leu347=) c.873A>C (p.Leu291=) | |
| 5 | g.80674996A>G | CA445159620 | MSH3 | c.1041A>G (p.Leu347=) c.873A>G (p.Leu291=) | |
| 5 | g.80674996A>T | CA3327785 | MSH3 | c.1041A>T (p.Leu347=) c.873A>T (p.Leu291=) | dbSNP ExAC |
| 5 | g.80674997A= | CA1558493192 | MSH3 | c.1042A= (p.Ile348=) c.874A= (p.Ile292=) | |
| 5 | g.80674997A>C | CA360267865 | MSH3 | c.1042A>C (p.Ile348Leu) c.874A>C (p.Ile292Leu) | ClinVar dbSNP |
| 5 | g.80674997A>G | CA360267863 | MSH3 | c.1042A>G (p.Ile348Val) c.874A>G (p.Ile292Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80674997A>T | CA360267866 | MSH3 | c.1042A>T (p.Ile348Phe) c.874A>T (p.Ile292Phe) | gnomAD v4 |
| 5 | g.80674998T>A | CA360267869 | MSH3 | c.1043T>A (p.Ile348Asn) c.875T>A (p.Ile292Asn) | dbSNP |
| 5 | g.80674998T>C | CA360267872 | MSH3 | c.1043T>C (p.Ile348Thr) c.875T>C (p.Ile292Thr) | |
| 5 | g.80674998T>G | CA360267870 | MSH3 | c.1043T>G (p.Ile348Ser) c.875T>G (p.Ile292Ser) | |
| 5 | g.80674999C>A | CA445159627 | MSH3 | c.1044C>A (p.Ile348=) c.876C>A (p.Ile292=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80674999C= | CA1558493193 | MSH3 | c.1044C= (p.Ile348=) c.876C= (p.Ile292=) | |
| 5 | g.80674999C>G | CA3327786 | MSH3 | c.1044C>G (p.Ile348Met) c.876C>G (p.Ile292Met) | ClinVar dbSNP ExAC gnomAD v2 |
| 5 | g.80674999C>T | CA445159629 | MSH3 | c.1044C>T (p.Ile348=) c.876C>T (p.Ile292=) | COSMIC COSMIC |
| 5 | g.80675000A>C | CA360267875 | MSH3 | c.1045A>C (p.Lys349Gln) c.877A>C (p.Lys293Gln) | |
| 5 | g.80675000A>G | CA360267877 | MSH3 | c.1045A>G (p.Lys349Glu) c.877A>G (p.Lys293Glu) | |
| 5 | g.80675000A>T | CA360267879 | MSH3 | c.1045A>T (p.Lys349Ter) c.877A>T (p.Lys293Ter) | gnomAD v4 |
| 5 | g.80675001A= | CA1558493194 | MSH3 | c.1046A= (p.Lys349=) c.878A= (p.Lys293=) | |
| 5 | g.80675001A>C | CA360267881 | MSH3 | c.1046A>C (p.Lys349Thr) c.878A>C (p.Lys293Thr) | |
| 5 | g.80675001A>G | CA3327787 | MSH3 | c.1046A>G (p.Lys349Arg) c.878A>G (p.Lys293Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675001A>T | CA360267883 | MSH3 | c.1046A>T (p.Lys349Met) c.878A>T (p.Lys293Met) | |
| 5 | g.80675002G>A | CA445159636 | MSH3 | c.1047G>A (p.Lys349=) c.879G>A (p.Lys293=) | ClinVar |
| 5 | g.80675002G>C | CA360267885 | MSH3 | c.1047G>C (p.Lys349Asn) c.879G>C (p.Lys293Asn) | |
| 5 | g.80675002G>T | CA360267887 | MSH3 | c.1047G>T (p.Lys349Asn) c.879G>T (p.Lys293Asn) | |
| 5 | g.80675003C>A | CA360267889 | MSH3 | c.1048C>A (p.Leu350Met) c.880C>A (p.Leu294Met) | |
| 5 | g.80675003C>G | CA360267891 | MSH3 | c.1048C>G (p.Leu350Val) c.880C>G (p.Leu294Val) | ClinVar dbSNP |
| 5 | g.80675003C>T | CA445159639 | MSH3 | c.1048C>T (p.Leu350=) c.880C>T (p.Leu294=) | |
| 5 | g.80675004T>A | CA360267895 | MSH3 | c.1049T>A (p.Leu350Gln) c.881T>A (p.Leu294Gln) | |
| 5 | g.80675004T>C | CA360267893 | MSH3 | c.1049T>C (p.Leu350Pro) c.881T>C (p.Leu294Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675004T>G | CA360267894 | MSH3 | c.1049T>G (p.Leu350Arg) c.881T>G (p.Leu294Arg) | |
| 5 | g.80675004T= | CA1558493195 | MSH3 | c.1049T= (p.Leu350=) c.881T= (p.Leu294=) | |
| 5 | g.80675005G>A | CA445159647 | MSH3 | c.1050G>A (p.Leu350=) c.882G>A (p.Leu294=) | ClinVar |
| 5 | g.80675005G>C | CA445159645 | MSH3 | c.1050G>C (p.Leu350=) c.882G>C (p.Leu294=) | |
| 5 | g.80675005G>T | CA445159644 | MSH3 | c.1050G>T (p.Leu350=) c.882G>T (p.Leu294=) | |
| 5 | g.80675006G>A | CA3327788 | MSH3 | c.1051G>A (p.Asp351Asn) c.883G>A (p.Asp295Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675006G>C | CA360267897 | MSH3 | c.1051G>C (p.Asp351His) c.883G>C (p.Asp295His) | |
| 5 | g.80675006G= | CA1558493196 | MSH3 | c.1051G= (p.Asp351=) c.883G= (p.Asp295=) | |
| 5 | g.80675006G>T | CA360267899 | MSH3 | c.1051G>T (p.Asp351Tyr) c.883G>T (p.Asp295Tyr) | COSMIC COSMIC |
| 5 | g.80675007A= | CA1558493204 | MSH3 | c.1052A= (p.Asp351=) c.884A= (p.Asp295=) | |
| 5 | g.80675007A>C | CA360267901 | MSH3 | c.1052A>C (p.Asp351Ala) c.884A>C (p.Asp295Ala) | |
| 5 | g.80675007A>G | CA3327789 | MSH3 | c.1052A>G (p.Asp351Gly) c.884A>G (p.Asp295Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675007A>T | CA360267903 | MSH3 | c.1052A>T (p.Asp351Val) c.884A>T (p.Asp295Val) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675008T>A | CA360267905 | MSH3 | c.1053T>A (p.Asp351Glu) c.885T>A (p.Asp295Glu) | |
| 5 | g.80675008T>C | CA445159656 | MSH3 | c.1053T>C (p.Asp351=) c.885T>C (p.Asp295=) | |
| 5 | g.80675008T>G | CA360267907 | MSH3 | c.1053T>G (p.Asp351Glu) c.885T>G (p.Asp295Glu) | |
| 5 | g.80675009G>A | CA360267909 | MSH3 | c.1054G>A (p.Asp352Asn) c.886G>A (p.Asp296Asn) | gnomAD v4 |
| 5 | g.80675009G>C | CA360267911 | MSH3 | c.1054G>C (p.Asp352His) c.886G>C (p.Asp296His) | ClinVar dbSNP |
| 5 | g.80675009G= | CA1558493209 | MSH3 | c.1054G= (p.Asp352=) c.886G= (p.Asp296=) | |
| 5 | g.80675009G>T | CA360267912 | MSH3 | c.1054G>T (p.Asp352Tyr) c.886G>T (p.Asp296Tyr) | |
| 5 | g.80675010A>C | CA360267915 | MSH3 | c.1055A>C (p.Asp352Ala) c.887A>C (p.Asp296Ala) | |
| 5 | g.80675010A>G | CA360267917 | MSH3 | c.1055A>G (p.Asp352Gly) c.887A>G (p.Asp296Gly) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675010A>T | CA360267914 | MSH3 | c.1055A>T (p.Asp352Val) c.887A>T (p.Asp296Val) | ClinVar gnomAD v4 |
| 5 | g.80675011T>A | CA360267919 | MSH3 | c.1056T>A (p.Asp352Glu) c.888T>A (p.Asp296Glu) | |
| 5 | g.80675011T>C | CA445159662 | MSH3 | c.1056T>C (p.Asp352=) c.888T>C (p.Asp296=) | |
| 5 | g.80675011T>G | CA360267921 | MSH3 | c.1056T>G (p.Asp352Glu) c.888T>G (p.Asp296Glu) | |
| 5 | g.80675012G>A | CA360267923 | MSH3 | c.1057G>A (p.Ala353Thr) c.889G>A (p.Ala297Thr) | ClinVar dbSNP |
| 5 | g.80675012G>C | CA360267924 | MSH3 | c.1057G>C (p.Ala353Pro) c.889G>C (p.Ala297Pro) | ClinVar |
| 5 | g.80675012G= | CA1558493213 | MSH3 | c.1057G= (p.Ala353=) c.889G= (p.Ala297=) | |
| 5 | g.80675012G>T | CA360267926 | MSH3 | c.1057G>T (p.Ala353Ser) c.889G>T (p.Ala297Ser) | |
| 5 | g.80675013C>A | CA360267932 | MSH3 | c.1058C>A (p.Ala353Asp) c.890C>A (p.Ala297Asp) | |
| 5 | g.80675013C>G | CA360267930 | MSH3 | c.1058C>G (p.Ala353Gly) c.890C>G (p.Ala297Gly) | ClinVar |
| 5 | g.80675013C>T | CA360267929 | MSH3 | c.1058C>T (p.Ala353Val) c.890C>T (p.Ala297Val) | ClinVar dbSNP |
| 5 | g.80675015_80675047dup | CA915943434 | MSH3 | c.1060_1092dup (p.Ser364_Thr365insValAsnValAspGluIleMetThrAspThrSer) c.892_924dup (p.Ser308_Thr309insValAsnValAspGluIleMetThrAspThrSer) | ClinVar dbSNP |
| 5 | g.80675014T>A | CA445159669 | MSH3 | c.1059T>A (p.Ala353=) c.891T>A (p.Ala297=) | |
| 5 | g.80675014T>C | CA445159671 | MSH3 | c.1059T>C (p.Ala353=) c.891T>C (p.Ala297=) | |
| 5 | g.80675014T>G | CA445159672 | MSH3 | c.1059T>G (p.Ala353=) c.891T>G (p.Ala297=) | ClinVar |
| 5 | g.80675014T= | CA1558493223 | MSH3 | c.1059T= (p.Ala353=) c.891T= (p.Ala297=) | |
| 5 | g.80675015_80675016del | CA2578350233 | MSH3 | c.1060_1061del (p.Val354LysfsTer3) c.892_893del (p.Val298LysfsTer3) | |
| 5 | g.80675017_80675022del | CA2580073614 | MSH3 | c.1062_1067del (p.Asn355_Val356del) c.894_899del (p.Asn299_Val300del) | ClinVar |
| 5 | g.80675015G>A | CA360267934 | MSH3 | c.1060G>A (p.Val354Ile) c.892G>A (p.Val298Ile) | dbSNP |
| 5 | g.80675015G>C | CA360267936 | MSH3 | c.1060G>C (p.Val354Leu) c.892G>C (p.Val298Leu) | |
| 5 | g.80675015G>T | CA360267937 | MSH3 | c.1060G>T (p.Val354Leu) c.892G>T (p.Val298Leu) | |
| 5 | g.80675015dup | CA915943435 | MSH3 | c.1060dup (p.Val354GlyfsTer4) c.892dup (p.Val298GlyfsTer4) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675016T>A | CA360267939 | MSH3 | c.1061T>A (p.Val354Glu) c.893T>A (p.Val298Glu) | |
| 5 | g.80675016T>C | CA360267940 | MSH3 | c.1061T>C (p.Val354Ala) c.893T>C (p.Val298Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675016T>G | CA360267941 | MSH3 | c.1061T>G (p.Val354Gly) c.893T>G (p.Val298Gly) | |
| 5 | g.80675016T= | CA1558493234 | MSH3 | c.1061T= (p.Val354=) c.893T= (p.Val298=) | |
| 5 | g.80675016_80675017delinsTA | CA1558493233 | MSH3 | c.1061_1062delinsTA (p.Val354=) c.893_894delinsTA (p.Val298=) | |
| 5 | g.80675017A>C | CA445159678 | MSH3 | c.1062A>C (p.Val354=) c.894A>C (p.Val298=) | |
| 5 | g.80675017A>G | CA445159680 | MSH3 | c.1062A>G (p.Val354=) c.894A>G (p.Val298=) | |
| 5 | g.80675017A>T | CA445159681 | MSH3 | c.1062A>T (p.Val354=) c.894A>T (p.Val298=) | |
| 5 | g.80675019del | CA121295132 | MSH3 | c.1064del (p.Asn355MetfsTer5) c.896del (p.Asn299MetfsTer5) | dbSNP |
| 5 | g.80675018A= | CA1558493242 | MSH3 | c.1063A= (p.Asn355=) c.895A= (p.Asn299=) | |
| 5 | g.80675018A>C | CA360267942 | MSH3 | c.1063A>C (p.Asn355His) c.895A>C (p.Asn299His) | ClinVar dbSNP |
| 5 | g.80675018A>G | CA3327790 | MSH3 | c.1063A>G (p.Asn355Asp) c.895A>G (p.Asn299Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675018A>T | CA360267943 | MSH3 | c.1063A>T (p.Asn355Tyr) c.895A>T (p.Asn299Tyr) | ClinVar dbSNP |
| 5 | g.80675019A>C | CA360267945 | MSH3 | c.1064A>C (p.Asn355Thr) c.896A>C (p.Asn299Thr) | |
| 5 | g.80675019A>G | CA360267946 | MSH3 | c.1064A>G (p.Asn355Ser) c.896A>G (p.Asn299Ser) | gnomAD v4 |
| 5 | g.80675019A>T | CA360267949 | MSH3 | c.1064A>T (p.Asn355Ile) c.896A>T (p.Asn299Ile) | |
| 5 | g.80675020T>A | CA360267953 | MSH3 | c.1065T>A (p.Asn355Lys) c.897T>A (p.Asn299Lys) | |
| 5 | g.80675020T>C | CA3327791 | MSH3 | c.1065T>C (p.Asn355=) c.897T>C (p.Asn299=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.80675020T>G | CA360267956 | MSH3 | c.1065T>G (p.Asn355Lys) c.897T>G (p.Asn299Lys) | ClinVar dbSNP |
| 5 | g.80675020T= | CA1558493246 | MSH3 | c.1065T= (p.Asn355=) c.897T= (p.Asn299=) | |
| 5 | g.80675021G>A | CA360267958 | MSH3 | c.1066G>A (p.Val356Ile) c.898G>A (p.Val300Ile) | ClinVar dbSNP |
| 5 | g.80675021G>C | CA360267960 | MSH3 | c.1066G>C (p.Val356Leu) c.898G>C (p.Val300Leu) | |
| 5 | g.80675021G>T | CA360267961 | MSH3 | c.1066G>T (p.Val356Phe) c.898G>T (p.Val300Phe) | gnomAD v4 |
| 5 | g.80675022T>A | CA360267963 | MSH3 | c.1067T>A (p.Val356Asp) c.899T>A (p.Val300Asp) | |
| 5 | g.80675022T>C | CA360267965 | MSH3 | c.1067T>C (p.Val356Ala) c.899T>C (p.Val300Ala) | |
| 5 | g.80675022T>G | CA360267967 | MSH3 | c.1067T>G (p.Val356Gly) c.899T>G (p.Val300Gly) | |
| 5 | g.80675023T>A | CA445159695 | MSH3 | c.1068T>A (p.Val356=) c.900T>A (p.Val300=) | |
| 5 | g.80675023T>C | CA445159696 | MSH3 | c.1068T>C (p.Val356=) c.900T>C (p.Val300=) | |
| 5 | g.80675023T>G | CA445159698 | MSH3 | c.1068T>G (p.Val356=) c.900T>G (p.Val300=) | |
| 5 | g.80675024G>A | CA360267972 | MSH3 | c.1069G>A (p.Asp357Asn) c.901G>A (p.Asp301Asn) | ClinVar |
| 5 | g.80675024G>C | CA360267971 | MSH3 | c.1069G>C (p.Asp357His) c.901G>C (p.Asp301His) | |
| 5 | g.80675024G>T | CA360267969 | MSH3 | c.1069G>T (p.Asp357Tyr) c.901G>T (p.Asp301Tyr) | |
| 5 | g.80675025A>C | CA360267973 | MSH3 | c.1070A>C (p.Asp357Ala) c.902A>C (p.Asp301Ala) | |
| 5 | g.80675025A>G | CA360267975 | MSH3 | c.1070A>G (p.Asp357Gly) c.902A>G (p.Asp301Gly) | |
| 5 | g.80675025A>T | CA360267977 | MSH3 | c.1070A>T (p.Asp357Val) c.902A>T (p.Asp301Val) | ClinVar |
| 5 | g.80675026T>A | CA360267978 | MSH3 | c.1071T>A (p.Asp357Glu) c.903T>A (p.Asp301Glu) | ClinVar dbSNP gnomAD v2 |
| 5 | g.80675026T>C | CA3327792 | MSH3 | c.1071T>C (p.Asp357=) c.903T>C (p.Asp301=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675026T>G | CA360267980 | MSH3 | c.1071T>G (p.Asp357Glu) c.903T>G (p.Asp301Glu) | gnomAD v4 |
| 5 | g.80675026T= | CA1558493250 | MSH3 | c.1071T= (p.Asp357=) c.903T= (p.Asp301=) | |
| 5 | g.80675027G>A | CA360267986 | MSH3 | c.1072G>A (p.Glu358Lys) c.904G>A (p.Glu302Lys) | gnomAD v4 |
| 5 | g.80675027G>C | CA360267983 | MSH3 | c.1072G>C (p.Glu358Gln) c.904G>C (p.Glu302Gln) | |
| 5 | g.80675027G>T | CA360267985 | MSH3 | c.1072G>T (p.Glu358Ter) c.904G>T (p.Glu302Ter) | |
| 5 | g.80675028A= | CA1558493261 | MSH3 | c.1073A= (p.Glu358=) c.905A= (p.Glu302=) | |
| 5 | g.80675028A>C | CA360267988 | MSH3 | c.1073A>C (p.Glu358Ala) c.905A>C (p.Glu302Ala) | ClinVar dbSNP |
| 5 | g.80675028A>G | CA360267990 | MSH3 | c.1073A>G (p.Glu358Gly) c.905A>G (p.Glu302Gly) | ClinVar |
| 5 | g.80675028A>T | CA360267991 | MSH3 | c.1073A>T (p.Glu358Val) c.905A>T (p.Glu302Val) | |
| 5 | g.80675029G>A | CA445159710 | MSH3 | c.1074G>A (p.Glu358=) c.906G>A (p.Glu302=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.80675029G>C | CA360267992 | MSH3 | c.1074G>C (p.Glu358Asp) c.906G>C (p.Glu302Asp) | ClinVar |
| 5 | g.80675029G= | CA1558493268 | MSH3 | c.1074G= (p.Glu358=) c.906G= (p.Glu302=) | |
| 5 | g.80675029G>T | CA360267993 | MSH3 | c.1074G>T (p.Glu358Asp) c.906G>T (p.Glu302Asp) | |
| 5 | g.80675030A= | CA1558493273 | MSH3 | c.1075A= (p.Ile359=) c.907A= (p.Ile303=) | |
| 5 | g.80675030A>C | CA360267996 | MSH3 | c.1075A>C (p.Ile359Leu) c.907A>C (p.Ile303Leu) | ClinVar dbSNP |
| 5 | g.80675030A>G | CA360267994 | MSH3 | c.1075A>G (p.Ile359Val) c.907A>G (p.Ile303Val) | ClinVar |
| 5 | g.80675030A>T | CA360267995 | MSH3 | c.1075A>T (p.Ile359Leu) c.907A>T (p.Ile303Leu) | |
| 5 | g.80675031T>A | CA360267997 | MSH3 | c.1076T>A (p.Ile359Lys) c.908T>A (p.Ile303Lys) | |
| 5 | g.80675031T>C | CA360267999 | MSH3 | c.1076T>C (p.Ile359Thr) c.908T>C (p.Ile303Thr) | |
| 5 | g.80675031T>G | CA360268000 | MSH3 | c.1076T>G (p.Ile359Arg) c.908T>G (p.Ile303Arg) | |
| 5 | g.80675032A>C | CA445159716 | MSH3 | c.1077A>C (p.Ile359=) c.909A>C (p.Ile303=) | |
| 5 | g.80675032A>G | CA360268002 | MSH3 | c.1077A>G (p.Ile359Met) c.909A>G (p.Ile303Met) | ClinVar |
| 5 | g.80675032A>T | CA445159718 | MSH3 | c.1077A>T (p.Ile359=) c.909A>T (p.Ile303=) | |
| 5 | g.80675033A= | CA1558493278 | MSH3 | c.1078A= (p.Met360=) c.910A= (p.Met304=) | |
| 5 | g.80675033A>C | CA360268004 | MSH3 | c.1078A>C (p.Met360Leu) c.910A>C (p.Met304Leu) | |
| 5 | g.80675033A>G | CA360268006 | MSH3 | c.1078A>G (p.Met360Val) c.910A>G (p.Met304Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.80675033A>T | CA360268008 | MSH3 | c.1078A>T (p.Met360Leu) c.910A>T (p.Met304Leu) | |
| 5 | g.80675034T>A | CA360268010 | MSH3 | c.1079T>A (p.Met360Lys) c.911T>A (p.Met304Lys) | |
| 5 | g.80675034T>C | CA360268012 | MSH3 | c.1079T>C (p.Met360Thr) c.911T>C (p.Met304Thr) | ClinVar dbSNP gnomAD v4 |
| 5 | g.80675034T>G | CA360268014 | MSH3 | c.1079T>G (p.Met360Arg) c.911T>G (p.Met304Arg) | |
| 5 | g.80675034T= | CA1558493285 | MSH3 | c.1079T= (p.Met360=) c.911T= (p.Met304=) | |
| 5 | g.80675035G>A | CA360268017 | MSH3 | c.1080G>A (p.Met360Ile) c.912G>A (p.Met304Ile) | |
| 5 | g.80675035G>C | CA3327793 | MSH3 | c.1080G>C (p.Met360Ile) c.912G>C (p.Met304Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.80675035G= | CA1558493289 | MSH3 | c.1080G= (p.Met360=) c.912G= (p.Met304=) | |
| 5 | g.80675035G>T | CA360268019 | MSH3 | c.1080G>T (p.Met360Ile) c.912G>T (p.Met304Ile) |