Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47795896_47805709delCA658655622FBXO11,MSH6c.163_3349+2del
c.460_3262+2del
n.544_4320+2del
c.460_2080+2del
c.460_3652+2del
c.460_1101+2del
c.460_3646+2del
c.238-2715_3256+2del
c.169+2491_170-6451del (n.169+2491_170-6451del)
c.*124+2290_*125-6451del (n.*124+2290_*125-6451del)
c.458-2715_*2993+2del
c.-443_2740+2del
c.-279-2715_2740+2del
c.-2637_550+2del
c.277_3463+2del
2g.47799557_47804482dupCA10575504FBXO11,MSH6c.1277_3142-428dup
c.1574_3173-1136dup
n.1658_3523-428dup
c.1574_1873-428dup
c.1580_3445-428dup
c.627+3494_894-428dup
c.731_2330-1136dup
c.1574_3439-428dup
c.1184_3049-428dup
c.169+3714_169+8639dup (n.169+3714_169+8639dup)
c.*124+3513_*124+8438dup (n.*124+3513_*124+8438dup)
c.*921_*2786-428dup
c.668_2533-428dup
c.-1523_335-420dup
c.1391_3256-428dup
ClinVar
2g.47799955_47804552delCA1139655753FBXO11,MSH6c.1675_3142-358del
c.1972_3173-1066del
n.2056_3523-358del
c.1606+366_1873-358del
c.1978_3445-358del
c.628-3465_894-358del
c.1129_2330-1066del
c.1972_3439-358del
c.1582_3049-358del
c.169+3644_169+8241del (n.169+3644_169+8241del)
c.*124+3443_*124+8040del (n.*124+3443_*124+8040del)
c.*1319_*2786-358del
c.1066_2533-358del
c.-1125_335-350del
c.1789_3256-358del
ClinVar
2g.47800849_47800852delCA2697548134FBXO11,MSH6c.2569_2572del (p.Glu857AsnfsTer11)
c.2866_2869del (p.Glu956AsnfsTer11)
n.2950_2953del
c.1606+1260_1606+1263del (n.1606+1260_1606+1263del)
c.2872_2875del (p.Glu958AsnfsTer11)
c.628-2571_628-2568del (n.628-2571_628-2568del)
c.2023_2026del (p.Glu675AsnfsTer11)
c.2476_2479del (p.Glu826AsnfsTer11)
c.169+7344_169+7347del (n.169+7344_169+7347del)
c.*124+7143_*124+7146del (n.*124+7143_*124+7146del)
c.*2213_*2216del (n.*2213_*2216del)
c.1960_1963del (p.Glu654AsnfsTer11)
c.2863_2866del (p.Glu955AsnfsTer11)
c.-231_-228del (n.-231_-228del)
c.2683_2686del (p.Glu895AsnfsTer11)
ClinVar
2g.47800850A>CCA346755964FBXO11,MSH6c.2570A>C (p.Glu857Ala)
c.2867A>C (p.Glu956Ala)
n.2951A>C
c.1606+1261A>C (n.1606+1261A>C)
c.2873A>C (p.Glu958Ala)
c.628-2570A>C (n.628-2570A>C)
c.2024A>C (p.Glu675Ala)
c.2477A>C (p.Glu826Ala)
c.169+7345T>G (n.169+7345T>G)
c.*124+7144T>G (n.*124+7144T>G)
c.*2214A>C (n.*2214A>C)
c.1961A>C (p.Glu654Ala)
c.2864A>C (p.Glu955Ala)
c.-230A>C (n.-230A>C)
c.2684A>C (p.Glu895Ala)
2g.47800850A>GCA346755966FBXO11,MSH6c.2570A>G (p.Glu857Gly)
c.2867A>G (p.Glu956Gly)
n.2951A>G
c.1606+1261A>G (n.1606+1261A>G)
c.2873A>G (p.Glu958Gly)
c.628-2570A>G (n.628-2570A>G)
c.2024A>G (p.Glu675Gly)
c.2477A>G (p.Glu826Gly)
c.169+7345T>C (n.169+7345T>C)
c.*124+7144T>C (n.*124+7144T>C)
c.*2214A>G (n.*2214A>G)
c.1961A>G (p.Glu654Gly)
c.2864A>G (p.Glu955Gly)
c.-230A>G (n.-230A>G)
c.2684A>G (p.Glu895Gly)
COSMIC
2g.47800850A>TCA346755968FBXO11,MSH6c.2570A>T (p.Glu857Val)
c.2867A>T (p.Glu956Val)
n.2951A>T
c.1606+1261A>T (n.1606+1261A>T)
c.2873A>T (p.Glu958Val)
c.628-2570A>T (n.628-2570A>T)
c.2024A>T (p.Glu675Val)
c.2477A>T (p.Glu826Val)
c.169+7345T>A (n.169+7345T>A)
c.*124+7144T>A (n.*124+7144T>A)
c.*2214A>T (n.*2214A>T)
c.1961A>T (p.Glu654Val)
c.2864A>T (p.Glu955Val)
c.-230A>T (n.-230A>T)
c.2684A>T (p.Glu895Val)
dbSNP
2g.47800851G>ACA426121967FBXO11,MSH6c.2571G>A (p.Glu857=)
c.2868G>A (p.Glu956=)
n.2952G>A
c.1606+1262G>A (n.1606+1262G>A)
c.2874G>A (p.Glu958=)
c.628-2569G>A (n.628-2569G>A)
c.2025G>A (p.Glu675=)
c.2478G>A (p.Glu826=)
c.169+7344C>T (n.169+7344C>T)
c.*124+7143C>T (n.*124+7143C>T)
c.*2215G>A (n.*2215G>A)
c.1962G>A (p.Glu654=)
c.2865G>A (p.Glu955=)
c.-229G>A (n.-229G>A)
c.2685G>A (p.Glu895=)
ClinVar dbSNP
2g.47800851G>CCA346755969FBXO11,MSH6c.2571G>C (p.Glu857Asp)
c.2868G>C (p.Glu956Asp)
n.2952G>C
c.1606+1262G>C (n.1606+1262G>C)
c.2874G>C (p.Glu958Asp)
c.628-2569G>C (n.628-2569G>C)
c.2025G>C (p.Glu675Asp)
c.2478G>C (p.Glu826Asp)
c.169+7344C>G (n.169+7344C>G)
c.*124+7143C>G (n.*124+7143C>G)
c.*2215G>C (n.*2215G>C)
c.1962G>C (p.Glu654Asp)
c.2865G>C (p.Glu955Asp)
c.-229G>C (n.-229G>C)
c.2685G>C (p.Glu895Asp)
dbSNP
2g.47800851G=CA2496049905FBXO11,MSH6c.2571G= (p.Glu857=)
c.2868G= (p.Glu956=)
n.2952G=
c.1606+1262G= (n.1606+1262G=)
c.2874G= (p.Glu958=)
c.628-2569G= (n.628-2569G=)
c.2025G= (p.Glu675=)
c.2478G= (p.Glu826=)
c.169+7344C= (n.169+7344C=)
c.*124+7143C= (n.*124+7143C=)
c.*2215G= (n.*2215G=)
c.1962G= (p.Glu654=)
c.2865G= (p.Glu955=)
c.-229G= (n.-229G=)
c.2685G= (p.Glu895=)
2g.47800851G>TCA346755970FBXO11,MSH6c.2571G>T (p.Glu857Asp)
c.2868G>T (p.Glu956Asp)
n.2952G>T
c.1606+1262G>T (n.1606+1262G>T)
c.2874G>T (p.Glu958Asp)
c.628-2569G>T (n.628-2569G>T)
c.2025G>T (p.Glu675Asp)
c.2478G>T (p.Glu826Asp)
c.169+7344C>A (n.169+7344C>A)
c.*124+7143C>A (n.*124+7143C>A)
c.*2215G>T (n.*2215G>T)
c.1962G>T (p.Glu654Asp)
c.2865G>T (p.Glu955Asp)
c.-229G>T (n.-229G>T)
c.2685G>T (p.Glu895Asp)
dbSNP
2g.47800852A=CA2496049906FBXO11,MSH6c.2572A= (p.Lys858=)
c.2869A= (p.Lys957=)
n.2953A=
c.1606+1263A= (n.1606+1263A=)
c.2875A= (p.Lys959=)
c.628-2568A= (n.628-2568A=)
c.2026A= (p.Lys676=)
c.2479A= (p.Lys827=)
c.169+7343T= (n.169+7343T=)
c.*124+7142T= (n.*124+7142T=)
c.*2216A= (n.*2216A=)
c.1963A= (p.Lys655=)
c.2866A= (p.Lys956=)
c.-228A= (n.-228A=)
c.2686A= (p.Lys896=)
2g.47800852A>CCA346755974FBXO11,MSH6c.2572A>C (p.Lys858Gln)
c.2869A>C (p.Lys957Gln)
n.2953A>C
c.1606+1263A>C (n.1606+1263A>C)
c.2875A>C (p.Lys959Gln)
c.628-2568A>C (n.628-2568A>C)
c.2026A>C (p.Lys676Gln)
c.2479A>C (p.Lys827Gln)
c.169+7343T>G (n.169+7343T>G)
c.*124+7142T>G (n.*124+7142T>G)
c.*2216A>C (n.*2216A>C)
c.1963A>C (p.Lys655Gln)
c.2866A>C (p.Lys956Gln)
c.-228A>C (n.-228A>C)
c.2686A>C (p.Lys896Gln)
2g.47800852A>GCA10577280FBXO11,MSH6c.2572A>G (p.Lys858Glu)
c.2869A>G (p.Lys957Glu)
n.2953A>G
c.1606+1263A>G (n.1606+1263A>G)
c.2875A>G (p.Lys959Glu)
c.628-2568A>G (n.628-2568A>G)
c.2026A>G (p.Lys676Glu)
c.2479A>G (p.Lys827Glu)
c.169+7343T>C (n.169+7343T>C)
c.*124+7142T>C (n.*124+7142T>C)
c.*2216A>G (n.*2216A>G)
c.1963A>G (p.Lys655Glu)
c.2866A>G (p.Lys956Glu)
c.-228A>G (n.-228A>G)
c.2686A>G (p.Lys896Glu)
ClinVar dbSNP
2g.47800852A>TCA346755976FBXO11,MSH6c.2572A>T (p.Lys858Ter)
c.2869A>T (p.Lys957Ter)
n.2953A>T
c.1606+1263A>T (n.1606+1263A>T)
c.2875A>T (p.Lys959Ter)
c.628-2568A>T (n.628-2568A>T)
c.2026A>T (p.Lys676Ter)
c.2479A>T (p.Lys827Ter)
c.169+7343T>A (n.169+7343T>A)
c.*124+7142T>A (n.*124+7142T>A)
c.*2216A>T (n.*2216A>T)
c.1963A>T (p.Lys655Ter)
c.2866A>T (p.Lys956Ter)
c.-228A>T (n.-228A>T)
c.2686A>T (p.Lys896Ter)
2g.47800853A>CCA346755979FBXO11,MSH6c.2573A>C (p.Lys858Thr)
c.2870A>C (p.Lys957Thr)
n.2954A>C
c.1606+1264A>C (n.1606+1264A>C)
c.2876A>C (p.Lys959Thr)
c.628-2567A>C (n.628-2567A>C)
c.2027A>C (p.Lys676Thr)
c.2480A>C (p.Lys827Thr)
c.169+7342T>G (n.169+7342T>G)
c.*124+7141T>G (n.*124+7141T>G)
c.*2217A>C (n.*2217A>C)
c.1964A>C (p.Lys655Thr)
c.2867A>C (p.Lys956Thr)
c.-227A>C (n.-227A>C)
c.2687A>C (p.Lys896Thr)
dbSNP
2g.47800853A>GCA346755980FBXO11,MSH6c.2573A>G (p.Lys858Arg)
c.2870A>G (p.Lys957Arg)
n.2954A>G
c.1606+1264A>G (n.1606+1264A>G)
c.2876A>G (p.Lys959Arg)
c.628-2567A>G (n.628-2567A>G)
c.2027A>G (p.Lys676Arg)
c.2480A>G (p.Lys827Arg)
c.169+7342T>C (n.169+7342T>C)
c.*124+7141T>C (n.*124+7141T>C)
c.*2217A>G (n.*2217A>G)
c.1964A>G (p.Lys655Arg)
c.2867A>G (p.Lys956Arg)
c.-227A>G (n.-227A>G)
c.2687A>G (p.Lys896Arg)
2g.47800853A>TCA346755982FBXO11,MSH6c.2573A>T (p.Lys858Ile)
c.2870A>T (p.Lys957Ile)
n.2954A>T
c.1606+1264A>T (n.1606+1264A>T)
c.2876A>T (p.Lys959Ile)
c.628-2567A>T (n.628-2567A>T)
c.2027A>T (p.Lys676Ile)
c.2480A>T (p.Lys827Ile)
c.169+7342T>A (n.169+7342T>A)
c.*124+7141T>A (n.*124+7141T>A)
c.*2217A>T (n.*2217A>T)
c.1964A>T (p.Lys655Ile)
c.2867A>T (p.Lys956Ile)
c.-227A>T (n.-227A>T)
c.2687A>T (p.Lys896Ile)
dbSNP
2g.47800853_47800855delinsAACCA2496049907FBXO11,MSH6c.2573_2575delinsAAC (p.Lys858=)
c.2870_2872delinsAAC (p.Lys957=)
n.2954_2956delinsAAC
c.1606+1264_1606+1266delinsAAC (n.1606+1264_1606+1266delinsAAC)
c.2876_2878delinsAAC (p.Lys959=)
c.628-2567_628-2565delinsAAC (n.628-2567_628-2565delinsAAC)
c.2027_2029delinsAAC (p.Lys676=)
c.2480_2482delinsAAC (p.Lys827=)
c.169+7340_169+7342delinsGTT (n.169+7340_169+7342delinsGTT)
c.*124+7139_*124+7141delinsGTT (n.*124+7139_*124+7141delinsGTT)
c.*2217_*2219delinsAAC (n.*2217_*2219delinsAAC)
c.1964_1966delinsAAC (p.Lys655=)
c.2867_2869delinsAAC (p.Lys956=)
c.-227_-225delinsAAC (n.-227_-225delinsAAC)
c.2687_2689delinsAAC (p.Lys896=)
2g.47800853_47800855delinsGAACA1139655910FBXO11,MSH6c.2573_2575delinsGAA (p.Lys858_Gln859delinsArgLys)
c.2870_2872delinsGAA (p.Lys957_Gln958delinsArgLys)
n.2954_2956delinsGAA
c.1606+1264_1606+1266delinsGAA (n.1606+1264_1606+1266delinsGAA)
c.2876_2878delinsGAA (p.Lys959_Gln960delinsArgLys)
c.628-2567_628-2565delinsGAA (n.628-2567_628-2565delinsGAA)
c.2027_2029delinsGAA (p.Lys676_Gln677delinsArgLys)
c.2480_2482delinsGAA (p.Lys827_Gln828delinsArgLys)
c.169+7340_169+7342delinsTTC (n.169+7340_169+7342delinsTTC)
c.*124+7139_*124+7141delinsTTC (n.*124+7139_*124+7141delinsTTC)
c.*2217_*2219delinsGAA (n.*2217_*2219delinsGAA)
c.1964_1966delinsGAA (p.Lys655_Gln656delinsArgLys)
c.2867_2869delinsGAA (p.Lys956_Gln957delinsArgLys)
c.-227_-225delinsGAA (n.-227_-225delinsGAA)
c.2687_2689delinsGAA (p.Lys896_Gln897delinsArgLys)
ClinVar dbSNP
2g.47800854A=CA2496049908FBXO11,MSH6c.2574A= (p.Lys858=)
c.2871A= (p.Lys957=)
n.2955A=
c.1606+1265A= (n.1606+1265A=)
c.2877A= (p.Lys959=)
c.628-2566A= (n.628-2566A=)
c.2028A= (p.Lys676=)
c.2481A= (p.Lys827=)
c.169+7341T= (n.169+7341T=)
c.*124+7140T= (n.*124+7140T=)
c.*2218A= (n.*2218A=)
c.1965A= (p.Lys655=)
c.2868A= (p.Lys956=)
c.-226A= (n.-226A=)
c.2688A= (p.Lys896=)
2g.47800854A>CCA346755985FBXO11,MSH6c.2574A>C (p.Lys858Asn)
c.2871A>C (p.Lys957Asn)
n.2955A>C
c.1606+1265A>C (n.1606+1265A>C)
c.2877A>C (p.Lys959Asn)
c.628-2566A>C (n.628-2566A>C)
c.2028A>C (p.Lys676Asn)
c.2481A>C (p.Lys827Asn)
c.169+7341T>G (n.169+7341T>G)
c.*124+7140T>G (n.*124+7140T>G)
c.*2218A>C (n.*2218A>C)
c.1965A>C (p.Lys655Asn)
c.2868A>C (p.Lys956Asn)
c.-226A>C (n.-226A>C)
c.2688A>C (p.Lys896Asn)
dbSNP
2g.47800854A>GCA069726FBXO11,MSH6c.2574A>G (p.Lys858=)
c.2871A>G (p.Lys957=)
n.2955A>G
c.1606+1265A>G (n.1606+1265A>G)
c.2877A>G (p.Lys959=)
c.628-2566A>G (n.628-2566A>G)
c.2028A>G (p.Lys676=)
c.2481A>G (p.Lys827=)
c.169+7341T>C (n.169+7341T>C)
c.*124+7140T>C (n.*124+7140T>C)
c.*2218A>G (n.*2218A>G)
c.1965A>G (p.Lys655=)
c.2868A>G (p.Lys956=)
c.-226A>G (n.-226A>G)
c.2688A>G (p.Lys896=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47800854A>TCA346755986FBXO11,MSH6c.2574A>T (p.Lys858Asn)
c.2871A>T (p.Lys957Asn)
n.2955A>T
c.1606+1265A>T (n.1606+1265A>T)
c.2877A>T (p.Lys959Asn)
c.628-2566A>T (n.628-2566A>T)
c.2028A>T (p.Lys676Asn)
c.2481A>T (p.Lys827Asn)
c.169+7341T>A (n.169+7341T>A)
c.*124+7140T>A (n.*124+7140T>A)
c.*2218A>T (n.*2218A>T)
c.1965A>T (p.Lys655Asn)
c.2868A>T (p.Lys956Asn)
c.-226A>T (n.-226A>T)
c.2688A>T (p.Lys896Asn)
ClinVar dbSNP
2g.47800855_47800856dupCA2695200589FBXO11,MSH6c.2575_2576dup (p.Gln859HisfsTer11)
c.2872_2873dup (p.Gln958HisfsTer11)
n.2956_2957dup
c.1606+1266_1606+1267dup (n.1606+1266_1606+1267dup)
c.2878_2879dup (p.Gln960HisfsTer11)
c.628-2565_628-2564dup (n.628-2565_628-2564dup)
c.2029_2030dup (p.Gln677HisfsTer11)
c.2482_2483dup (p.Gln828HisfsTer11)
c.169+7340_169+7341dup (n.169+7340_169+7341dup)
c.*124+7139_*124+7140dup (n.*124+7139_*124+7140dup)
c.*2219_*2220dup (n.*2219_*2220dup)
c.1966_1967dup (p.Gln656HisfsTer11)
c.2869_2870dup (p.Gln957HisfsTer11)
c.-225_-224dup (n.-225_-224dup)
c.2689_2690dup (p.Gln897HisfsTer11)
ClinVar
2g.47800855C>ACA346755988FBXO11,MSH6c.2575C>A (p.Gln859Lys)
c.2872C>A (p.Gln958Lys)
n.2956C>A
c.1606+1266C>A (n.1606+1266C>A)
c.2878C>A (p.Gln960Lys)
c.628-2565C>A (n.628-2565C>A)
c.2029C>A (p.Gln677Lys)
c.2482C>A (p.Gln828Lys)
c.169+7340G>T (n.169+7340G>T)
c.*124+7139G>T (n.*124+7139G>T)
c.*2219C>A (n.*2219C>A)
c.1966C>A (p.Gln656Lys)
c.2869C>A (p.Gln957Lys)
c.-225C>A (n.-225C>A)
c.2689C>A (p.Gln897Lys)
dbSNP
2g.47800855C=CA2496049911FBXO11,MSH6c.2575C= (p.Gln859=)
c.2872C= (p.Gln958=)
n.2956C=
c.1606+1266C= (n.1606+1266C=)
c.2878C= (p.Gln960=)
c.628-2565C= (n.628-2565C=)
c.2029C= (p.Gln677=)
c.2482C= (p.Gln828=)
c.169+7340G= (n.169+7340G=)
c.*124+7139G= (n.*124+7139G=)
c.*2219C= (n.*2219C=)
c.1966C= (p.Gln656=)
c.2869C= (p.Gln957=)
c.-225C= (n.-225C=)
c.2689C= (p.Gln897=)
2g.47800855C>GCA346755990FBXO11,MSH6c.2575C>G (p.Gln859Glu)
c.2872C>G (p.Gln958Glu)
n.2956C>G
c.1606+1266C>G (n.1606+1266C>G)
c.2878C>G (p.Gln960Glu)
c.628-2565C>G (n.628-2565C>G)
c.2029C>G (p.Gln677Glu)
c.2482C>G (p.Gln828Glu)
c.169+7340G>C (n.169+7340G>C)
c.*124+7139G>C (n.*124+7139G>C)
c.*2219C>G (n.*2219C>G)
c.1966C>G (p.Gln656Glu)
c.2869C>G (p.Gln957Glu)
c.-225C>G (n.-225C>G)
c.2689C>G (p.Gln897Glu)
ClinVar dbSNP
2g.47800855C>TCA346755992FBXO11,MSH6c.2575C>T (p.Gln859Ter)
c.2872C>T (p.Gln958Ter)
n.2956C>T
c.1606+1266C>T (n.1606+1266C>T)
c.2878C>T (p.Gln960Ter)
c.628-2565C>T (n.628-2565C>T)
c.2029C>T (p.Gln677Ter)
c.2482C>T (p.Gln828Ter)
c.169+7340G>A (n.169+7340G>A)
c.*124+7139G>A (n.*124+7139G>A)
c.*2219C>T (n.*2219C>T)
c.1966C>T (p.Gln656Ter)
c.2869C>T (p.Gln957Ter)
c.-225C>T (n.-225C>T)
c.2689C>T (p.Gln897Ter)
ClinVar dbSNP
2g.47800855_47800856delinsCACA2496049909FBXO11,MSH6c.2575_2576delinsCA (p.Gln859=)
c.2872_2873delinsCA (p.Gln958=)
n.2956_2957delinsCA
c.1606+1266_1606+1267delinsCA (n.1606+1266_1606+1267delinsCA)
c.2878_2879delinsCA (p.Gln960=)
c.628-2565_628-2564delinsCA (n.628-2565_628-2564delinsCA)
c.2029_2030delinsCA (p.Gln677=)
c.2482_2483delinsCA (p.Gln828=)
c.169+7339_169+7340delinsTG (n.169+7339_169+7340delinsTG)
c.*124+7138_*124+7139delinsTG (n.*124+7138_*124+7139delinsTG)
c.*2219_*2220delinsCA (n.*2219_*2220delinsCA)
c.1966_1967delinsCA (p.Gln656=)
c.2869_2870delinsCA (p.Gln957=)
c.-225_-224delinsCA (n.-225_-224delinsCA)
c.2689_2690delinsCA (p.Gln897=)
2g.47800855_47800857delinsCAGCA2496049910FBXO11,MSH6c.2575_2577delinsCAG (p.Gln859=)
c.2872_2874delinsCAG (p.Gln958=)
n.2956_2958delinsCAG
c.1606+1266_1606+1268delinsCAG (n.1606+1266_1606+1268delinsCAG)
c.2878_2880delinsCAG (p.Gln960=)
c.628-2565_628-2563delinsCAG (n.628-2565_628-2563delinsCAG)
c.2029_2031delinsCAG (p.Gln677=)
c.2482_2484delinsCAG (p.Gln828=)
c.169+7338_169+7340delinsCTG (n.169+7338_169+7340delinsCTG)
c.*124+7137_*124+7139delinsCTG (n.*124+7137_*124+7139delinsCTG)
c.*2219_*2221delinsCAG (n.*2219_*2221delinsCAG)
c.1966_1968delinsCAG (p.Gln656=)
c.2869_2871delinsCAG (p.Gln957=)
c.-225_-223delinsCAG (n.-225_-223delinsCAG)
c.2689_2691delinsCAG (p.Gln897=)
2g.47800856delCA915943936FBXO11,MSH6c.2576del (p.Gln859ArgfsTer10)
c.2873del (p.Gln958ArgfsTer10)
n.2957del
c.1606+1267del (n.1606+1267del)
c.2879del (p.Gln960ArgfsTer10)
c.628-2564del (n.628-2564del)
c.2030del (p.Gln677ArgfsTer10)
c.2483del (p.Gln828ArgfsTer10)
c.169+7339del (n.169+7339del)
c.*124+7138del (n.*124+7138del)
c.*2220del (n.*2220del)
c.1967del (p.Gln656ArgfsTer10)
c.2870del (p.Gln957ArgfsTer10)
c.-224del (n.-224del)
c.2690del (p.Gln897ArgfsTer10)
ClinVar dbSNP
2g.47800856A=CA2496049913FBXO11,MSH6c.2576A= (p.Gln859=)
c.2873A= (p.Gln958=)
n.2957A=
c.1606+1267A= (n.1606+1267A=)
c.2879A= (p.Gln960=)
c.628-2564A= (n.628-2564A=)
c.2030A= (p.Gln677=)
c.2483A= (p.Gln828=)
c.169+7339T= (n.169+7339T=)
c.*124+7138T= (n.*124+7138T=)
c.*2220A= (n.*2220A=)
c.1967A= (p.Gln656=)
c.2870A= (p.Gln957=)
c.-224A= (n.-224A=)
c.2690A= (p.Gln897=)
2g.47800856A>CCA346755996FBXO11,MSH6c.2576A>C (p.Gln859Pro)
c.2873A>C (p.Gln958Pro)
n.2957A>C
c.1606+1267A>C (n.1606+1267A>C)
c.2879A>C (p.Gln960Pro)
c.628-2564A>C (n.628-2564A>C)
c.2030A>C (p.Gln677Pro)
c.2483A>C (p.Gln828Pro)
c.169+7339T>G (n.169+7339T>G)
c.*124+7138T>G (n.*124+7138T>G)
c.*2220A>C (n.*2220A>C)
c.1967A>C (p.Gln656Pro)
c.2870A>C (p.Gln957Pro)
c.-224A>C (n.-224A>C)
c.2690A>C (p.Gln897Pro)
ClinVar dbSNP gnomAD v4
2g.47800856A>GCA10578123FBXO11,MSH6c.2576A>G (p.Gln859Arg)
c.2873A>G (p.Gln958Arg)
n.2957A>G
c.1606+1267A>G (n.1606+1267A>G)
c.2879A>G (p.Gln960Arg)
c.628-2564A>G (n.628-2564A>G)
c.2030A>G (p.Gln677Arg)
c.2483A>G (p.Gln828Arg)
c.169+7339T>C (n.169+7339T>C)
c.*124+7138T>C (n.*124+7138T>C)
c.*2220A>G (n.*2220A>G)
c.1967A>G (p.Gln656Arg)
c.2870A>G (p.Gln957Arg)
c.-224A>G (n.-224A>G)
c.2690A>G (p.Gln897Arg)
ClinVar dbSNP
2g.47800856A>TCA346755995FBXO11,MSH6c.2576A>T (p.Gln859Leu)
c.2873A>T (p.Gln958Leu)
n.2957A>T
c.1606+1267A>T (n.1606+1267A>T)
c.2879A>T (p.Gln960Leu)
c.628-2564A>T (n.628-2564A>T)
c.2030A>T (p.Gln677Leu)
c.2483A>T (p.Gln828Leu)
c.169+7339T>A (n.169+7339T>A)
c.*124+7138T>A (n.*124+7138T>A)
c.*2220A>T (n.*2220A>T)
c.1967A>T (p.Gln656Leu)
c.2870A>T (p.Gln957Leu)
c.-224A>T (n.-224A>T)
c.2690A>T (p.Gln897Leu)
ClinVar dbSNP
2g.47800856_47800857delCA658683237FBXO11,MSH6c.2576_2577del (p.Gln859ProfsTer7)
c.2873_2874del (p.Gln958ProfsTer7)
n.2957_2958del
c.1606+1267_1606+1268del (n.1606+1267_1606+1268del)
c.2879_2880del (p.Gln960ProfsTer7)
c.628-2564_628-2563del (n.628-2564_628-2563del)
c.2030_2031del (p.Gln677ProfsTer7)
c.2483_2484del (p.Gln828ProfsTer7)
c.169+7338_169+7339del (n.169+7338_169+7339del)
c.*124+7137_*124+7138del (n.*124+7137_*124+7138del)
c.*2220_*2221del (n.*2220_*2221del)
c.1967_1968del (p.Gln656ProfsTer7)
c.2870_2871del (p.Gln957ProfsTer7)
c.-224_-223del (n.-224_-223del)
c.2690_2691del (p.Gln897ProfsTer7)
ClinVar dbSNP
2g.47800856_47800868delinsAGCGCAACAGAATCA2496049912FBXO11,MSH6c.2576_2588delinsAGCGCAACAGAAT (p.Gln859=)
c.2873_2885delinsAGCGCAACAGAAT (p.Gln958=)
n.2957_2969delinsAGCGCAACAGAAT
c.1606+1267_1606+1279delinsAGCGCAACAGAAT (n.1606+1267_1606+1279delinsAGCGCAACAGAAT)
c.2879_2891delinsAGCGCAACAGAAT (p.Gln960=)
c.628-2564_628-2552delinsAGCGCAACAGAAT (n.628-2564_628-2552delinsAGCGCAACAGAAT)
c.2030_2042delinsAGCGCAACAGAAT (p.Gln677=)
c.2483_2495delinsAGCGCAACAGAAT (p.Gln828=)
c.169+7327_169+7339delinsATTCTGTTGCGCT (n.169+7327_169+7339delinsATTCTGTTGCGCT)
c.*124+7126_*124+7138delinsATTCTGTTGCGCT (n.*124+7126_*124+7138delinsATTCTGTTGCGCT)
c.*2220_*2232delinsAGCGCAACAGAAT (n.*2220_*2232delinsAGCGCAACAGAAT)
c.1967_1979delinsAGCGCAACAGAAT (p.Gln656=)
c.2870_2882delinsAGCGCAACAGAAT (p.Gln957=)
c.-224_-212delinsAGCGCAACAGAAT (n.-224_-212delinsAGCGCAACAGAAT)
c.2690_2702delinsAGCGCAACAGAAT (p.Gln897=)
2g.47800857G>ACA426121975FBXO11,MSH6c.2577G>A (p.Gln859=)
c.2874G>A (p.Gln958=)
n.2958G>A
c.1606+1268G>A (n.1606+1268G>A)
c.2880G>A (p.Gln960=)
c.628-2563G>A (n.628-2563G>A)
c.2031G>A (p.Gln677=)
c.2484G>A (p.Gln828=)
c.169+7338C>T (n.169+7338C>T)
c.*124+7137C>T (n.*124+7137C>T)
c.*2221G>A (n.*2221G>A)
c.1968G>A (p.Gln656=)
c.2871G>A (p.Gln957=)
c.-223G>A (n.-223G>A)
c.2691G>A (p.Gln897=)
ClinVar dbSNP
2g.47800857G>CCA346755999FBXO11,MSH6c.2577G>C (p.Gln859His)
c.2874G>C (p.Gln958His)
n.2958G>C
c.1606+1268G>C (n.1606+1268G>C)
c.2880G>C (p.Gln960His)
c.628-2563G>C (n.628-2563G>C)
c.2031G>C (p.Gln677His)
c.2484G>C (p.Gln828His)
c.169+7338C>G (n.169+7338C>G)
c.*124+7137C>G (n.*124+7137C>G)
c.*2221G>C (n.*2221G>C)
c.1968G>C (p.Gln656His)
c.2871G>C (p.Gln957His)
c.-223G>C (n.-223G>C)
c.2691G>C (p.Gln897His)
dbSNP
2g.47800857G=CA2496049914FBXO11,MSH6c.2577G= (p.Gln859=)
c.2874G= (p.Gln958=)
n.2958G=
c.1606+1268G= (n.1606+1268G=)
c.2880G= (p.Gln960=)
c.628-2563G= (n.628-2563G=)
c.2031G= (p.Gln677=)
c.2484G= (p.Gln828=)
c.169+7338C= (n.169+7338C=)
c.*124+7137C= (n.*124+7137C=)
c.*2221G= (n.*2221G=)
c.1968G= (p.Gln656=)
c.2871G= (p.Gln957=)
c.-223G= (n.-223G=)
c.2691G= (p.Gln897=)
2g.47800857G>TCA346756000FBXO11,MSH6c.2577G>T (p.Gln859His)
c.2874G>T (p.Gln958His)
n.2958G>T
c.1606+1268G>T (n.1606+1268G>T)
c.2880G>T (p.Gln960His)
c.628-2563G>T (n.628-2563G>T)
c.2031G>T (p.Gln677His)
c.2484G>T (p.Gln828His)
c.169+7338C>A (n.169+7338C>A)
c.*124+7137C>A (n.*124+7137C>A)
c.*2221G>T (n.*2221G>T)
c.1968G>T (p.Gln656His)
c.2871G>T (p.Gln957His)
c.-223G>T (n.-223G>T)
c.2691G>T (p.Gln897His)
2g.47800857_47800868delCA915943937FBXO11,MSH6c.2577_2588del (p.Gln859_Ile863delinsHis)
c.2874_2885del (p.Gln958_Ile962delinsHis)
n.2958_2969del
c.1606+1268_1606+1279del (n.1606+1268_1606+1279del)
c.2880_2891del (p.Gln960_Ile964delinsHis)
c.628-2563_628-2552del (n.628-2563_628-2552del)
c.2031_2042del (p.Gln677_Ile681delinsHis)
c.2484_2495del (p.Gln828_Ile832delinsHis)
c.169+7327_169+7338del (n.169+7327_169+7338del)
c.*124+7126_*124+7137del (n.*124+7126_*124+7137del)
c.*2221_*2232del (n.*2221_*2232del)
c.1968_1979del (p.Gln656_Ile660delinsHis)
c.2871_2882del (p.Gln957_Ile961delinsHis)
c.-223_-212del (n.-223_-212del)
c.2691_2702del (p.Gln897_Ile901delinsHis)
ClinVar dbSNP
2g.47800858C>ACA346756002FBXO11,MSH6c.2578C>A (p.Arg860Ser)
c.2875C>A (p.Arg959Ser)
n.2959C>A
c.1606+1269C>A (n.1606+1269C>A)
c.2881C>A (p.Arg961Ser)
c.628-2562C>A (n.628-2562C>A)
c.2032C>A (p.Arg678Ser)
c.2485C>A (p.Arg829Ser)
c.169+7337G>T (n.169+7337G>T)
c.*124+7136G>T (n.*124+7136G>T)
c.*2222C>A (n.*2222C>A)
c.1969C>A (p.Arg657Ser)
c.2872C>A (p.Arg958Ser)
c.-222C>A (n.-222C>A)
c.2692C>A (p.Arg898Ser)
ClinVar dbSNP
2g.47800858C=CA2496049915FBXO11,MSH6c.2578C= (p.Arg860=)
c.2875C= (p.Arg959=)
n.2959C=
c.1606+1269C= (n.1606+1269C=)
c.2881C= (p.Arg961=)
c.628-2562C= (n.628-2562C=)
c.2032C= (p.Arg678=)
c.2485C= (p.Arg829=)
c.169+7337G= (n.169+7337G=)
c.*124+7136G= (n.*124+7136G=)
c.*2222C= (n.*2222C=)
c.1969C= (p.Arg657=)
c.2872C= (p.Arg958=)
c.-222C= (n.-222C=)
c.2692C= (p.Arg898=)
2g.47800858C>GCA346756004FBXO11,MSH6c.2578C>G (p.Arg860Gly)
c.2875C>G (p.Arg959Gly)
n.2959C>G
c.1606+1269C>G (n.1606+1269C>G)
c.2881C>G (p.Arg961Gly)
c.628-2562C>G (n.628-2562C>G)
c.2032C>G (p.Arg678Gly)
c.2485C>G (p.Arg829Gly)
c.169+7337G>C (n.169+7337G>C)
c.*124+7136G>C (n.*124+7136G>C)
c.*2222C>G (n.*2222C>G)
c.1969C>G (p.Arg657Gly)
c.2872C>G (p.Arg958Gly)
c.-222C>G (n.-222C>G)
c.2692C>G (p.Arg898Gly)
dbSNP
2g.47800858C>TCA011024FBXO11,MSH6c.2578C>T (p.Arg860Cys)
c.2875C>T (p.Arg959Cys)
n.2959C>T
c.1606+1269C>T (n.1606+1269C>T)
c.2881C>T (p.Arg961Cys)
c.628-2562C>T (n.628-2562C>T)
c.2032C>T (p.Arg678Cys)
c.2485C>T (p.Arg829Cys)
c.169+7337G>A (n.169+7337G>A)
c.*124+7136G>A (n.*124+7136G>A)
c.*2222C>T (n.*2222C>T)
c.1969C>T (p.Arg657Cys)
c.2872C>T (p.Arg958Cys)
c.-222C>T (n.-222C>T)
c.2692C>T (p.Arg898Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47800859G>ACA011033FBXO11,MSH6c.2579G>A (p.Arg860His)
c.2876G>A (p.Arg959His)
n.2960G>A
c.1606+1270G>A (n.1606+1270G>A)
c.2882G>A (p.Arg961His)
c.628-2561G>A (n.628-2561G>A)
c.2033G>A (p.Arg678His)
c.2486G>A (p.Arg829His)
c.169+7336C>T (n.169+7336C>T)
c.*124+7135C>T (n.*124+7135C>T)
c.*2223G>A (n.*2223G>A)
c.1970G>A (p.Arg657His)
c.2873G>A (p.Arg958His)
c.-221G>A (n.-221G>A)
c.2693G>A (p.Arg898His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.47800859G>CCA346756008FBXO11,MSH6c.2579G>C (p.Arg860Pro)
c.2876G>C (p.Arg959Pro)
n.2960G>C
c.1606+1270G>C (n.1606+1270G>C)
c.2882G>C (p.Arg961Pro)
c.628-2561G>C (n.628-2561G>C)
c.2033G>C (p.Arg678Pro)
c.2486G>C (p.Arg829Pro)
c.169+7336C>G (n.169+7336C>G)
c.*124+7135C>G (n.*124+7135C>G)
c.*2223G>C (n.*2223G>C)
c.1970G>C (p.Arg657Pro)
c.2873G>C (p.Arg958Pro)
c.-221G>C (n.-221G>C)
c.2693G>C (p.Arg898Pro)
ClinVar dbSNP
2g.47800859G=CA2496049916FBXO11,MSH6c.2579G= (p.Arg860=)
c.2876G= (p.Arg959=)
n.2960G=
c.1606+1270G= (n.1606+1270G=)
c.2882G= (p.Arg961=)
c.628-2561G= (n.628-2561G=)
c.2033G= (p.Arg678=)
c.2486G= (p.Arg829=)
c.169+7336C= (n.169+7336C=)
c.*124+7135C= (n.*124+7135C=)
c.*2223G= (n.*2223G=)
c.1970G= (p.Arg657=)
c.2873G= (p.Arg958=)
c.-221G= (n.-221G=)
c.2693G= (p.Arg898=)

Number of alleles fetched