Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47401439_47411294delCA331194 ClinVar
2g.47403192_47408555delCA2581463442MSH2c.1_366del
c.-31+17_168del
n.73_438del
n.63_428del
2g.47403280_47410368delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTCA658760387MSH2c.89_641delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
c.-30-80_443delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
n.161_713delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
n.151_703delinsAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATT
2g.47408384_47408403delinsCTTTTTTTTTTTTTAAGGAGCA2495830005MSH2c.212-17_214delinsCTTTTTTTTTTTTTAAGGAG
c.14-17_16delinsCTTTTTTTTTTTTTAAGGAG
n.284-17_286delinsCTTTTTTTTTTTTTAAGGAG
n.274-17_276delinsCTTTTTTTTTTTTTAAGGAG
2g.47408385_47408403delCA1139656928MSH2c.212-16_214del
c.14-16_16del
n.284-16_286del
n.274-16_276del
 ClinVar dbSNP
2g.47408396_47408551delinsTTAAGGAGCAAAGAATCTGCAGAGTGTTGTGCTTAGTAAAATGAATTTTGAATCTTTTGTAAAAGATCTTCTTCTGGTTCGTCAGTATAGAGTTGAAGTTTATAAGAATAGAGCTGGAAATAAGGCATCCAAGGAGAATGATTGGTATTTGGCATACA2495830047MSH2c.212-5_362delinsTTAAGGAGCAAAGAATCTGCAGAGTGTTGTGCTTAGTAAAATGAATTTTGAATCTTTTGTAAAAGATCTTCTTCTGGTTCGTCAGTATAGAGTTGAAGTTTATAAGAATAGAGCTGGAAATAAGGCATCCAAGGAGAATGATTGGTATTTGGCATA
c.14-5_164delinsTTAAGGAGCAAAGAATCTGCAGAGTGTTGTGCTTAGTAAAATGAATTTTGAATCTTTTGTAAAAGATCTTCTTCTGGTTCGTCAGTATAGAGTTGAAGTTTATAAGAATAGAGCTGGAAATAAGGCATCCAAGGAGAATGATTGGTATTTGGCATA
n.284-5_434delinsTTAAGGAGCAAAGAATCTGCAGAGTGTTGTGCTTAGTAAAATGAATTTTGAATCTTTTGTAAAAGATCTTCTTCTGGTTCGTCAGTATAGAGTTGAAGTTTATAAGAATAGAGCTGGAAATAAGGCATCCAAGGAGAATGATTGGTATTTGGCATA
n.274-5_424delinsTTAAGGAGCAAAGAATCTGCAGAGTGTTGTGCTTAGTAAAATGAATTTTGAATCTTTTGTAAAAGATCTTCTTCTGGTTCGTCAGTATAGAGTTGAAGTTTATAAGAATAGAGCTGGAAATAAGGCATCCAAGGAGAATGATTGGTATTTGGCATA
2g.47408397_47408552delCA2499215995MSH2c.212-4_363del
c.14-4_165del
n.284-4_435del
n.274-4_425del
 ClinVar dbSNP
2g.47408397_47408402delinsTAAGGACA2495830057MSH2c.212-4_213delinsTAAGGA
c.14-4_15delinsTAAGGA
n.284-4_285delinsTAAGGA
n.274-4_275delinsTAAGGA
2g.47408402_47408556delCA645372532MSH2c.213_366+1del
c.15_168+1del
n.285_438+1del
n.275_428+1del
 ClinVar dbSNP
2g.47408398_47408400delCA2658945781MSH2c.212-3_212-1del (n.212-3_212-1del)
c.14-3_14-1del (n.14-3_14-1del)
n.284-3_284-1del
n.274-3_274-1del
 gnomAD v4
2g.47408398_47408401delinsAAGGCA2495830075MSH2c.212-3_212delinsAAGG
c.14-3_14delinsAAGG
n.284-3_284delinsAAGG
n.274-3_274delinsAAGG
2g.47408398_47408402delCA915943879MSH2c.212-3_213del
c.14-3_15del
n.284-3_285del
n.274-3_275del
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47408399_47408402delCA1030269389MSH2c.212-2_213del
c.14-2_15del
n.284-2_285del
n.274-2_275del
 gnomAD v3 gnomAD v4
2g.47408398_47408403delCA1030269390MSH2c.212-3_214del
c.14-3_16del
n.284-3_286del
n.274-3_276del
 gnomAD v3 gnomAD v4
2g.47408400_47408406delCA2658945783MSH2c.212-1_217del
c.14-1_19del
n.284-1_289del
n.274-1_279del
 gnomAD v4
2g.47408401_47408408delCA1139656929MSH2c.212_219del
c.14_21del
n.284_291del
n.274_281del
2g.47408399_47408400delinsAGCA2495830081MSH2c.212-2_212-1delinsAG (n.212-2_212-1delinsAG)
c.14-2_14-1delinsAG (n.14-2_14-1delinsAG)
n.284-2_284-1delinsAG
n.274-2_274-1delinsAG
2g.47408401_47408403delCA1649251MSH2c.212_214del
c.14_16del
n.284_286del
n.274_276del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47408399_47408410delinsAGGAGCAAAGAACA2495830083MSH2c.212-2_221delinsAGGAGCAAAGAA
c.14-2_23delinsAGGAGCAAAGAA
n.284-2_293delinsAGGAGCAAAGAA
n.274-2_283delinsAGGAGCAAAGAA
2g.47408399_47408556delCA2499215996MSH2c.212-2_366+1del
c.14-2_168+1del
n.284-2_438+1del
n.274-2_428+1del
 ClinVar dbSNP
2g.47408400_47409267delCA2499215997MSH2c.212-1_366+712del
c.14-1_168+712del
n.284-1_438+712del
n.274-1_428+712del
 ClinVar dbSNP
2g.47408402_47410373delCA2581463448MSH2c.213_645+1del
c.15_447+1del
n.285_717+1del
n.275_707+1del
2g.47408400G>ACA020080MSH2c.212-1G>A (n.212-1G>A)
c.14-1G>A (n.14-1G>A)
n.284-1G>A
n.274-1G>A
 ClinVar dbSNP gnomAD v4
2g.47408400G>CCA346729449MSH2c.212-1G>C (n.212-1G>C)
c.14-1G>C (n.14-1G>C)
n.284-1G>C
n.274-1G>C
 dbSNP
2g.47408400G=CA2495830101MSH2c.212-1G= (n.212-1G=)
c.14-1G= (n.14-1G=)
n.284-1G=
n.274-1G=
2g.47408400G>TCA346729448MSH2c.212-1G>T (n.212-1G>T)
c.14-1G>T (n.14-1G>T)
n.284-1G>T
n.274-1G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47408401delCA1139656930MSH2c.212del
c.14del
n.284del
n.274del
 ClinVar dbSNP
2g.47408400_47408410delinsCACCA10577925MSH2c.212-1_221delinsCAC
c.14-1_23delinsCAC
n.284-1_293delinsCAC
n.274-1_283delinsCAC
 ClinVar dbSNP
2g.47408400_47408454dupCA2699268416MSH2c.212-1_265dup
c.14-1_67dup
n.284-1_337dup
n.274-1_327dup
 dbSNP
2g.47408400_47408556dupCA2499215998MSH2c.212-1_366+1dup
c.14-1_168+1dup
n.284-1_438+1dup
n.274-1_428+1dup
 ClinVar
2g.47408401G>ACA16617553MSH2c.212G>A (p.Gly71Glu)
c.14G>A (p.Gly5Glu)
n.284G>A
n.274G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47408401G>CCA346729450MSH2c.212G>C (p.Gly71Ala)
c.14G>C (p.Gly5Ala)
n.284G>C
n.274G>C
 dbSNP
2g.47408401G=CA2495830107MSH2c.212G= (p.Gly71=)
c.14G= (p.Gly5=)
n.284G=
n.274G=
2g.47408401G>TCA346729451MSH2c.212G>T (p.Gly71Val)
c.14G>T (p.Gly5Val)
n.284G>T
n.274G>T
 dbSNP gnomAD v4 COSMIC
2g.47408402_47408419delCA645531408MSH2c.213_230del (p.Ala72_Ser77del)
c.15_32del (p.Ala6_Ser11del)
n.285_302del
n.275_292del
 COSMIC
2g.47408401_47408402insTTTTCA1030269445MSH2c.212_213insTTTT (p.Ala72PhefsTer11)
c.14_15insTTTT (p.Ala6PhefsTer11)
n.284_285insTTTT
n.274_275insTTTT
 gnomAD v3 gnomAD v4
2g.47408402A=CA2495830111MSH2c.213A= (p.Gly71=)
c.15A= (p.Gly5=)
n.285A=
n.275A=
2g.47408402A>CCA425965638MSH2c.213A>C (p.Gly71=)
c.15A>C (p.Gly5=)
n.285A>C
n.275A>C
2g.47408402A>GCA10581992MSH2c.213A>G (p.Gly71=)
c.15A>G (p.Gly5=)
n.285A>G
n.275A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47408402A>TCA425965639MSH2c.213A>T (p.Gly71=)
c.15A>T (p.Gly5=)
n.285A>T
n.275A>T
 dbSNP gnomAD v3 gnomAD v4
2g.47408402_47408413delinsAGCAAAGAATCTCA2495830114MSH2c.213_224delinsAGCAAAGAATCT (p.Gly71=)
c.15_26delinsAGCAAAGAATCT (p.Gly5=)
n.285_296delinsAGCAAAGAATCT
n.275_286delinsAGCAAAGAATCT
2g.47408402_47408403insTTTTTCA1030269458MSH2c.213_214insTTTTT (p.Ala72PhefsTer14)
c.15_16insTTTTT (p.Ala6PhefsTer14)
n.285_286insTTTTT
n.275_276insTTTTT
 gnomAD v3 gnomAD v4
2g.47408403G>ACA346729453MSH2c.214G>A (p.Ala72Thr)
c.16G>A (p.Ala6Thr)
n.286G>A
n.276G>A
 ClinVar dbSNP gnomAD v4
2g.47408403G>CCA346729454MSH2c.214G>C (p.Ala72Pro)
c.16G>C (p.Ala6Pro)
n.286G>C
n.276G>C
 dbSNP
2g.47408403G=CA2495830123MSH2c.214G= (p.Ala72=)
c.16G= (p.Ala6=)
n.286G=
n.276G=
2g.47408403G>TCA346729452MSH2c.214G>T (p.Ala72Ser)
c.16G>T (p.Ala6Ser)
n.286G>T
n.276G>T
 ClinVar dbSNP gnomAD v4
2g.47408406_47408416delCA645369199MSH2c.217_227del (p.Lys73GlufsTer5)
c.19_29del (p.Lys7GlufsTer5)
n.289_299del
n.279_289del
 ClinVar dbSNP
2g.47408403_47408404insTTTTTTCA913090554MSH2c.214_215insTTTTTT (p.Ala72delinsValPheSer)
c.16_17insTTTTTT (p.Ala6delinsValPheSer)
n.286_287insTTTTTT
n.276_277insTTTTTT
 gnomAD v3 gnomAD v4
2g.47408404C>ACA346729455MSH2c.215C>A (p.Ala72Glu)
c.17C>A (p.Ala6Glu)
n.287C>A
n.277C>A
 ClinVar dbSNP gnomAD v4
2g.47408404C=CA2495830128MSH2c.215C= (p.Ala72=)
c.17C= (p.Ala6=)
n.287C=
n.277C=

Number of alleles fetched