Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47795896_47805709delCA658655622MSH6c.460_3646+2del
c.238-2715_3256+2del
c.163_3349+2del
c.169+2491_170-6451del (p.=)
c.*124+2290_*125-6451del (p.=)
c.458-2715_*2993+2del
c.-443_2740+2del
c.-279-2715_2740+2del
c.-2637_550+2del
c.277_3463+2del
2g.47799557_47804482dupCA10575504MSH6c.1574_3439-428dup
c.1184_3049-428dup
c.1277_3142-428dup
c.169+3714_169+8639dup (p.=)
c.*124+3513_*124+8438dup (p.=)
c.*921_*2786-428dup
c.668_2533-428dup
c.-1523_335-420dup
c.1391_3256-428dup
ClinVar
2g.47799797_47799799delinsCTACA2496049006MSH6c.1814_1816delinsCTA (p.Thr605=)
c.1424_1426delinsCTA (p.Thr475=)
c.1517_1519delinsCTA (p.Thr506=)
c.169+8396_169+8398delinsTAG (p.=)
c.*124+8195_*124+8197delinsTAG (p.=)
c.*1161_*1163delinsCTA (p.=)
c.908_910delinsCTA (p.Thr303=)
c.1811_1813delinsCTA (p.Thr604=)
c.-1283_-1281delinsCTA (p.=)
c.1631_1633delinsCTA (p.Thr544=)
2g.47799798T>ACA426121171MSH6c.1815T>A (p.Thr605=)
c.1425T>A (p.Thr475=)
c.1518T>A (p.Thr506=)
c.169+8397A>T (p.=)
c.*124+8196A>T (p.=)
c.*1162T>A (p.=)
c.909T>A (p.Thr303=)
c.1812T>A (p.Thr604=)
c.-1282T>A (p.=)
c.1632T>A (p.Thr544=)
2g.47799798T>CCA426121172MSH6c.1815T>C (p.Thr605=)
c.1425T>C (p.Thr475=)
c.1518T>C (p.Thr506=)
c.169+8397A>G (p.=)
c.*124+8196A>G (p.=)
c.*1162T>C (p.=)
c.909T>C (p.Thr303=)
c.1812T>C (p.Thr604=)
c.-1282T>C (p.=)
c.1632T>C (p.Thr544=)
2g.47799798T>GCA426121173MSH6c.1815T>G (p.Thr605=)
c.1425T>G (p.Thr475=)
c.1518T>G (p.Thr506=)
c.169+8397A>C (p.=)
c.*124+8196A>C (p.=)
c.*1162T>G (p.=)
c.909T>G (p.Thr303=)
c.1812T>G (p.Thr604=)
c.-1282T>G (p.=)
c.1632T>G (p.Thr544=)
2g.47799798_47799799delCA16610988MSH6c.1815_1816del (p.Lys606AsnfsTer?)
c.1425_1426del (p.Lys476AsnfsTer?)
c.1518_1519del (p.Lys507AsnfsTer?)
c.169+8396_169+8397del (p.=)
c.*124+8195_*124+8196del (p.=)
c.*1162_*1163del (p.=)
c.909_910del (p.Lys304AsnfsTer?)
c.1812_1813del (p.Lys605AsnfsTer?)
c.-1282_-1281del (p.=)
c.1632_1633del (p.Lys545AsnfsTer?)
ClinVar dbSNP
2g.47799798_47799799delinsTACA2496049008MSH6c.1815_1816delinsTA (p.Thr605=)
c.1425_1426delinsTA (p.Thr475=)
c.1518_1519delinsTA (p.Thr506=)
c.169+8396_169+8397delinsTA (p.=)
c.*124+8195_*124+8196delinsTA (p.=)
c.*1162_*1163delinsTA (p.=)
c.909_910delinsTA (p.Thr303=)
c.1812_1813delinsTA (p.Thr604=)
c.-1282_-1281delinsTA (p.=)
c.1632_1633delinsTA (p.Thr544=)
2g.47799799A=CA2496049010MSH6c.1816A= (p.Lys606=)
c.1426A= (p.Lys476=)
c.1519A= (p.Lys507=)
c.169+8396T= (p.=)
c.*124+8195T= (p.=)
c.*1163A= (p.=)
c.910A= (p.Lys304=)
c.1813A= (p.Lys605=)
c.-1281A= (p.=)
c.1633A= (p.Lys545=)
2g.47799799A>CCA346749419MSH6c.1816A>C (p.Lys606Gln)
c.1426A>C (p.Lys476Gln)
c.1519A>C (p.Lys507Gln)
c.169+8396T>G (p.=)
c.*124+8195T>G (p.=)
c.*1163A>C (p.=)
c.910A>C (p.Lys304Gln)
c.1813A>C (p.Lys605Gln)
c.-1281A>C (p.=)
c.1633A>C (p.Lys545Gln)
2g.47799799A>GCA346749421MSH6c.1816A>G (p.Lys606Glu)
c.1426A>G (p.Lys476Glu)
c.1519A>G (p.Lys507Glu)
c.169+8396T>C (p.=)
c.*124+8195T>C (p.=)
c.*1163A>G (p.=)
c.910A>G (p.Lys304Glu)
c.1813A>G (p.Lys605Glu)
c.-1281A>G (p.=)
c.1633A>G (p.Lys545Glu)
ClinVar gnomAD
2g.47799799A>TCA346749423MSH6c.1816A>T (p.Lys606Ter)
c.1426A>T (p.Lys476Ter)
c.1519A>T (p.Lys507Ter)
c.169+8396T>A (p.=)
c.*124+8195T>A (p.=)
c.*1163A>T (p.=)
c.910A>T (p.Lys304Ter)
c.1813A>T (p.Lys605Ter)
c.-1281A>T (p.=)
c.1633A>T (p.Lys545Ter)
2g.47799802dupCA330389MSH6c.1819dup (p.Thr607AsnfsTer?)
c.1429dup (p.Thr477AsnfsTer?)
c.1522dup (p.Thr508AsnfsTer?)
c.169+8396dup (p.=)
c.*124+8195dup (p.=)
c.*1166dup (p.=)
c.913dup (p.Thr305AsnfsTer?)
c.1816dup (p.Thr606AsnfsTer?)
c.-1278dup (p.=)
c.1636dup (p.Thr546AsnfsTer?)
ClinVar dbSNP
2g.47799802delCA915943922MSH6c.1819del (p.Thr607GlnfsTer3)
c.1429del (p.Thr477GlnfsTer3)
c.1522del (p.Thr508GlnfsTer3)
c.169+8396del (p.=)
c.*124+8195del (p.=)
c.*1166del (p.=)
c.913del (p.Thr305GlnfsTer3)
c.1816del (p.Thr606GlnfsTer3)
c.-1278del (p.=)
c.1636del (p.Thr546GlnfsTer3)
ClinVar dbSNP
2g.47799799_47799803delinsAAAACCA2496049009MSH6c.1816_1820delinsAAAAC (p.Lys606=)
c.1426_1430delinsAAAAC (p.Lys476=)
c.1519_1523delinsAAAAC (p.Lys507=)
c.169+8392_169+8396delinsGTTTT (p.=)
c.*124+8191_*124+8195delinsGTTTT (p.=)
c.*1163_*1167delinsAAAAC (p.=)
c.910_914delinsAAAAC (p.Lys304=)
c.1813_1817delinsAAAAC (p.Lys605=)
c.-1281_-1277delinsAAAAC (p.=)
c.1633_1637delinsAAAAC (p.Lys545=)
2g.47799800A=CA2496049011MSH6c.1817A= (p.Lys606=)
c.1427A= (p.Lys476=)
c.1520A= (p.Lys507=)
c.169+8395T= (p.=)
c.*124+8194T= (p.=)
c.*1164A= (p.=)
c.911A= (p.Lys304=)
c.1814A= (p.Lys605=)
c.-1280A= (p.=)
c.1634A= (p.Lys545=)
2g.47799800A>CCA346749426MSH6c.1817A>C (p.Lys606Thr)
c.1427A>C (p.Lys476Thr)
c.1520A>C (p.Lys507Thr)
c.169+8395T>G (p.=)
c.*124+8194T>G (p.=)
c.*1164A>C (p.=)
c.911A>C (p.Lys304Thr)
c.1814A>C (p.Lys605Thr)
c.-1280A>C (p.=)
c.1634A>C (p.Lys545Thr)
2g.47799800A>GCA346749430MSH6c.1817A>G (p.Lys606Arg)
c.1427A>G (p.Lys476Arg)
c.1520A>G (p.Lys507Arg)
c.169+8395T>C (p.=)
c.*124+8194T>C (p.=)
c.*1164A>G (p.=)
c.911A>G (p.Lys304Arg)
c.1814A>G (p.Lys605Arg)
c.-1280A>G (p.=)
c.1634A>G (p.Lys545Arg)
ClinVar
2g.47799800A>TCA346749434MSH6c.1817A>T (p.Lys606Ile)
c.1427A>T (p.Lys476Ile)
c.1520A>T (p.Lys507Ile)
c.169+8395T>A (p.=)
c.*124+8194T>A (p.=)
c.*1164A>T (p.=)
c.911A>T (p.Lys304Ile)
c.1814A>T (p.Lys605Ile)
c.-1280A>T (p.=)
c.1634A>T (p.Lys545Ile)
2g.47799802_47799805delCA645369237MSH6c.1819_1822del (p.Thr607PhefsTer2)
c.1429_1432del (p.Thr477PhefsTer2)
c.1522_1525del (p.Thr508PhefsTer2)
c.169+8392_169+8395del (p.=)
c.*124+8191_*124+8194del (p.=)
c.*1166_*1169del (p.=)
c.913_916del (p.Thr305PhefsTer2)
c.1816_1819del (p.Thr606PhefsTer2)
c.-1278_-1275del (p.=)
c.1636_1639del (p.Thr546PhefsTer2)
ClinVar dbSNP
2g.47799801A=CA2496049012MSH6c.1818A= (p.Lys606=)
c.1428A= (p.Lys476=)
c.1521A= (p.Lys507=)
c.169+8394T= (p.=)
c.*124+8193T= (p.=)
c.*1165A= (p.=)
c.912A= (p.Lys304=)
c.1815A= (p.Lys605=)
c.-1279A= (p.=)
c.1635A= (p.Lys545=)
2g.47799801A>CCA346749437MSH6c.1818A>C (p.Lys606Asn)
c.1428A>C (p.Lys476Asn)
c.1521A>C (p.Lys507Asn)
c.169+8394T>G (p.=)
c.*124+8193T>G (p.=)
c.*1165A>C (p.=)
c.912A>C (p.Lys304Asn)
c.1815A>C (p.Lys605Asn)
c.-1279A>C (p.=)
c.1635A>C (p.Lys545Asn)
2g.47799801A>GCA426121176MSH6c.1818A>G (p.Lys606=)
c.1428A>G (p.Lys476=)
c.1521A>G (p.Lys507=)
c.169+8394T>C (p.=)
c.*124+8193T>C (p.=)
c.*1165A>G (p.=)
c.912A>G (p.Lys304=)
c.1815A>G (p.Lys605=)
c.-1279A>G (p.=)
c.1635A>G (p.Lys545=)
ClinVar
2g.47799801A>TCA346749440MSH6c.1818A>T (p.Lys606Asn)
c.1428A>T (p.Lys476Asn)
c.1521A>T (p.Lys507Asn)
c.169+8394T>A (p.=)
c.*124+8193T>A (p.=)
c.*1165A>T (p.=)
c.912A>T (p.Lys304Asn)
c.1815A>T (p.Lys605Asn)
c.-1279A>T (p.=)
c.1635A>T (p.Lys545Asn)
2g.47799802A=CA2496049013MSH6c.1819A= (p.Thr607=)
c.1429A= (p.Thr477=)
c.1522A= (p.Thr508=)
c.169+8393T= (p.=)
c.*124+8192T= (p.=)
c.*1166A= (p.=)
c.913A= (p.Thr305=)
c.1816A= (p.Thr606=)
c.-1278A= (p.=)
c.1636A= (p.Thr546=)
2g.47799802A>CCA346749443MSH6c.1819A>C (p.Thr607Pro)
c.1429A>C (p.Thr477Pro)
c.1522A>C (p.Thr508Pro)
c.169+8393T>G (p.=)
c.*124+8192T>G (p.=)
c.*1166A>C (p.=)
c.913A>C (p.Thr305Pro)
c.1816A>C (p.Thr606Pro)
c.-1278A>C (p.=)
c.1636A>C (p.Thr546Pro)
2g.47799802A>GCA346749445MSH6c.1819A>G (p.Thr607Ala)
c.1429A>G (p.Thr477Ala)
c.1522A>G (p.Thr508Ala)
c.169+8393T>C (p.=)
c.*124+8192T>C (p.=)
c.*1166A>G (p.=)
c.913A>G (p.Thr305Ala)
c.1816A>G (p.Thr606Ala)
c.-1278A>G (p.=)
c.1636A>G (p.Thr546Ala)
ClinVar
2g.47799802A>TCA346749449MSH6c.1819A>T (p.Thr607Ser)
c.1429A>T (p.Thr477Ser)
c.1522A>T (p.Thr508Ser)
c.169+8393T>A (p.=)
c.*124+8192T>A (p.=)
c.*1166A>T (p.=)
c.913A>T (p.Thr305Ser)
c.1816A>T (p.Thr606Ser)
c.-1278A>T (p.=)
c.1636A>T (p.Thr546Ser)
2g.47799803C>ACA346749458MSH6c.1820C>A (p.Thr607Lys)
c.1430C>A (p.Thr477Lys)
c.1523C>A (p.Thr508Lys)
c.169+8392G>T (p.=)
c.*124+8191G>T (p.=)
c.*1167C>A (p.=)
c.914C>A (p.Thr305Lys)
c.1817C>A (p.Thr606Lys)
c.-1277C>A (p.=)
c.1637C>A (p.Thr546Lys)
2g.47799803C=CA2496049014MSH6c.1820C= (p.Thr607=)
c.1430C= (p.Thr477=)
c.1523C= (p.Thr508=)
c.169+8392G= (p.=)
c.*124+8191G= (p.=)
c.*1167C= (p.=)
c.914C= (p.Thr305=)
c.1817C= (p.Thr606=)
c.-1277C= (p.=)
c.1637C= (p.Thr546=)
2g.47799803C>GCA009262MSH6c.1820C>G (p.Thr607Arg)
c.1430C>G (p.Thr477Arg)
c.1523C>G (p.Thr508Arg)
c.169+8392G>C (p.=)
c.*124+8191G>C (p.=)
c.*1167C>G (p.=)
c.914C>G (p.Thr305Arg)
c.1817C>G (p.Thr606Arg)
c.-1277C>G (p.=)
c.1637C>G (p.Thr546Arg)
ClinVar dbSNP
2g.47799803C>TCA346749453MSH6c.1820C>T (p.Thr607Ile)
c.1430C>T (p.Thr477Ile)
c.1523C>T (p.Thr508Ile)
c.169+8392G>A (p.=)
c.*124+8191G>A (p.=)
c.*1167C>T (p.=)
c.914C>T (p.Thr305Ile)
c.1817C>T (p.Thr606Ile)
c.-1277C>T (p.=)
c.1637C>T (p.Thr546Ile)
2g.47799804A=CA2496049015MSH6c.1821A= (p.Thr607=)
c.1431A= (p.Thr477=)
c.1524A= (p.Thr508=)
c.169+8391T= (p.=)
c.*124+8190T= (p.=)
c.*1168A= (p.=)
c.915A= (p.Thr305=)
c.1818A= (p.Thr606=)
c.-1276A= (p.=)
c.1638A= (p.Thr546=)
2g.47799804A>CCA426121180MSH6c.1821A>C (p.Thr607=)
c.1431A>C (p.Thr477=)
c.1524A>C (p.Thr508=)
c.169+8391T>G (p.=)
c.*124+8190T>G (p.=)
c.*1168A>C (p.=)
c.915A>C (p.Thr305=)
c.1818A>C (p.Thr606=)
c.-1276A>C (p.=)
c.1638A>C (p.Thr546=)
2g.47799804A>GCA426121182MSH6c.1821A>G (p.Thr607=)
c.1431A>G (p.Thr477=)
c.1524A>G (p.Thr508=)
c.169+8391T>C (p.=)
c.*124+8190T>C (p.=)
c.*1168A>G (p.=)
c.915A>G (p.Thr305=)
c.1818A>G (p.Thr606=)
c.-1276A>G (p.=)
c.1638A>G (p.Thr546=)
2g.47799804A>TCA426121183MSH6c.1821A>T (p.Thr607=)
c.1431A>T (p.Thr477=)
c.1524A>T (p.Thr508=)
c.169+8391T>A (p.=)
c.*124+8190T>A (p.=)
c.*1168A>T (p.=)
c.915A>T (p.Thr305=)
c.1818A>T (p.Thr606=)
c.-1276A>T (p.=)
c.1638A>T (p.Thr546=)
2g.47799805A=CA2496049016MSH6c.1822A= (p.Ile608=)
c.1432A= (p.Ile478=)
c.1525A= (p.Ile509=)
c.169+8390T= (p.=)
c.*124+8189T= (p.=)
c.*1169A= (p.=)
c.916A= (p.Ile306=)
c.1819A= (p.Ile607=)
c.-1275A= (p.=)
c.1639A= (p.Ile547=)
2g.47799805A>CCA346749461MSH6c.1822A>C (p.Ile608Leu)
c.1432A>C (p.Ile478Leu)
c.1525A>C (p.Ile509Leu)
c.169+8390T>G (p.=)
c.*124+8189T>G (p.=)
c.*1169A>C (p.=)
c.916A>C (p.Ile306Leu)
c.1819A>C (p.Ile607Leu)
c.-1275A>C (p.=)
c.1639A>C (p.Ile547Leu)
2g.47799805A>GCA009270MSH6c.1822A>G (p.Ile608Val)
c.1432A>G (p.Ile478Val)
c.1525A>G (p.Ile509Val)
c.169+8390T>C (p.=)
c.*124+8189T>C (p.=)
c.*1169A>G (p.=)
c.916A>G (p.Ile306Val)
c.1819A>G (p.Ile607Val)
c.-1275A>G (p.=)
c.1639A>G (p.Ile547Val)
ClinVar dbSNP ExAC gnomAD
2g.47799805A>TCA346749462MSH6c.1822A>T (p.Ile608Phe)
c.1432A>T (p.Ile478Phe)
c.1525A>T (p.Ile509Phe)
c.169+8390T>A (p.=)
c.*124+8189T>A (p.=)
c.*1169A>T (p.=)
c.916A>T (p.Ile306Phe)
c.1819A>T (p.Ile607Phe)
c.-1275A>T (p.=)
c.1639A>T (p.Ile547Phe)
ClinVar
2g.47799806T>ACA346749463MSH6c.1823T>A (p.Ile608Asn)
c.1433T>A (p.Ile478Asn)
c.1526T>A (p.Ile509Asn)
c.169+8389A>T (p.=)
c.*124+8188A>T (p.=)
c.*1170T>A (p.=)
c.917T>A (p.Ile306Asn)
c.1820T>A (p.Ile607Asn)
c.-1274T>A (p.=)
c.1640T>A (p.Ile547Asn)
2g.47799806T>CCA346749466MSH6c.1823T>C (p.Ile608Thr)
c.1433T>C (p.Ile478Thr)
c.1526T>C (p.Ile509Thr)
c.169+8389A>G (p.=)
c.*124+8188A>G (p.=)
c.*1170T>C (p.=)
c.917T>C (p.Ile306Thr)
c.1820T>C (p.Ile607Thr)
c.-1274T>C (p.=)
c.1640T>C (p.Ile547Thr)
ClinVar
2g.47799806T>GCA346749468MSH6c.1823T>G (p.Ile608Ser)
c.1433T>G (p.Ile478Ser)
c.1526T>G (p.Ile509Ser)
c.169+8389A>C (p.=)
c.*124+8188A>C (p.=)
c.*1170T>G (p.=)
c.917T>G (p.Ile306Ser)
c.1820T>G (p.Ile607Ser)
c.-1274T>G (p.=)
c.1640T>G (p.Ile547Ser)
2g.47799806T=CA2496049017MSH6c.1823T= (p.Ile608=)
c.1433T= (p.Ile478=)
c.1526T= (p.Ile509=)
c.169+8389A= (p.=)
c.*124+8188A= (p.=)
c.*1170T= (p.=)
c.917T= (p.Ile306=)
c.1820T= (p.Ile607=)
c.-1274T= (p.=)
c.1640T= (p.Ile547=)
2g.47799807T>ACA426121188MSH6c.1824T>A (p.Ile608=)
c.1434T>A (p.Ile478=)
c.1527T>A (p.Ile509=)
c.169+8388A>T (p.=)
c.*124+8187A>T (p.=)
c.*1171T>A (p.=)
c.918T>A (p.Ile306=)
c.1821T>A (p.Ile607=)
c.-1273T>A (p.=)
c.1641T>A (p.Ile547=)
2g.47799807T>CCA426121189MSH6c.1824T>C (p.Ile608=)
c.1434T>C (p.Ile478=)
c.1527T>C (p.Ile509=)
c.169+8388A>G (p.=)
c.*124+8187A>G (p.=)
c.*1171T>C (p.=)
c.918T>C (p.Ile306=)
c.1821T>C (p.Ile607=)
c.-1273T>C (p.=)
c.1641T>C (p.Ile547=)
ClinVar
2g.47799807T>GCA346749473MSH6c.1824T>G (p.Ile608Met)
c.1434T>G (p.Ile478Met)
c.1527T>G (p.Ile509Met)
c.169+8388A>C (p.=)
c.*124+8187A>C (p.=)
c.*1171T>G (p.=)
c.918T>G (p.Ile306Met)
c.1821T>G (p.Ile607Met)
c.-1273T>G (p.=)
c.1641T>G (p.Ile547Met)
2g.47799807T=CA2496049018MSH6c.1824T= (p.Ile608=)
c.1434T= (p.Ile478=)
c.1527T= (p.Ile509=)
c.169+8388A= (p.=)
c.*124+8187A= (p.=)
c.*1171T= (p.=)
c.918T= (p.Ile306=)
c.1821T= (p.Ile607=)
c.-1273T= (p.=)
c.1641T= (p.Ile547=)
2g.47799808C>ACA346749476MSH6c.1825C>A (p.Leu609Ile)
c.1435C>A (p.Leu479Ile)
c.1528C>A (p.Leu510Ile)
c.169+8387G>T (p.=)
c.*124+8186G>T (p.=)
c.*1172C>A (p.=)
c.919C>A (p.Leu307Ile)
c.1822C>A (p.Leu608Ile)
c.-1272C>A (p.=)
c.1642C>A (p.Leu548Ile)
ClinVar gnomAD
2g.47799808C=CA2496049019MSH6c.1825C= (p.Leu609=)
c.1435C= (p.Leu479=)
c.1528C= (p.Leu510=)
c.169+8387G= (p.=)
c.*124+8186G= (p.=)
c.*1172C= (p.=)
c.919C= (p.Leu307=)
c.1822C= (p.Leu608=)
c.-1272C= (p.=)
c.1642C= (p.Leu548=)

Number of alleles fetched