Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7669589_7676614delCA2499224945TP53c.-19_*21del
c.-21-1377_*21del
c.-19_*310del
c.-19_*222del
c.-253_*21del
c.-136_*222del
c.-136_*21del
c.-136_*310del
c.-136_983+1021del
ClinVar
17g.7669609_7676594delCA2581463470TP53c.1_1182del
c.-21-1358_786del
c.1_903del
c.1_1161del
c.1_994-3365del
c.1_782+4572del
c.1_*289del
c.1_*201del
c.-234_1065del
c.-117_*201del
c.1_1149del
c.-117_1065del
c.-117_*289del
c.-117_983+1000del
17g.7674861_7676624dupCA2573130640TP53c.-28_672dup
c.-21-1386_276dup
c.-28_393dup
c.-28_651dup
c.-25-3_672dup
n.112_928dup
c.-262_555dup
c.-145_555dup
c.-142-3_555dup
ClinVar
17g.7675197_7676153delCA645589160TP53c.216_415del
c.-21-917_19del
c.96+229_136del
c.216_394del
n.472_671del
c.99_298del
c.216_382del
COSMIC
17g.7675226_7676561delCA645589205TP53c.36_388del
c.-21-1323_-9del
c.36_109del
c.36_376-9del
n.175_644del
c.-199_271del
c.-82_271del
c.36_355del
COSMIC
17g.7675505_7676086delCA2580095057TP53c.283_376-269del
c.-21-850_-21-269del (n.-21-850_-21-269del)
c.96+296_97-269del (n.96+296_97-269del)
c.283_376-290del
n.539_632-269del
c.166_259-269del
c.283_341-267del
ClinVar
17g.7675972_7676086delinsCCAGCCCCTCAGGGCAACTGACCGTGCAAGTCACAGACTTGGCTGTCCCAGAATGCAAGAAGCCCAGACGGAAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGGACAGAAGACA2245932234TP53c.283_375+22delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG
c.-21-850_-21-736delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG (n.-21-850_-21-736delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG)
c.96+296_96+410delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG (n.96+296_96+410delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG)
n.539_631+22delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG
c.166_258+22delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG
c.283_340+53delinsTCTTCTGTCCCTTCCCAGAAAACCTACCAGGGCAGCTACGGTTTCCGTCTGGGCTTCTTGCATTCTGGGACAGCCAAGTCTGTGACTTGCACGGTCAGTTGCCCTGAGGGGCTGG
17g.7675973_7676086delCA16615710TP53c.283_375+21del
c.-21-850_-21-737del (n.-21-850_-21-737del)
c.96+296_96+409del (n.96+296_96+409del)
n.539_631+21del
c.166_258+21del
c.283_340+52del
ClinVar dbSNP
17g.7675995_7676194delCA645589234TP53c.179_375+3del
c.-21-954_-21-755del (n.-21-954_-21-755del)
c.96+192_96+391del (n.96+192_96+391del)
n.435_631+3del
c.62_258+3del
c.179_340+34del
COSMIC
17g.7675995_7676057delCA645589237TP53c.314_375+1del
c.-21-819_-21-757del (n.-21-819_-21-757del)
c.96+327_96+389del (n.96+327_96+389del)
n.570_631+1del
c.197_258+1del
c.314_340+32del
COSMIC
17g.7675995_7676052delCA645589238TP53c.318_375del (p.Tyr107ThrfsTer?)
c.-21-815_-21-758del (n.-21-815_-21-758del)
c.96+331_96+388del (n.96+331_96+388del)
c.318_375del (p.Ser106ArgfsTer?)
n.574_631del
c.201_258del (p.Tyr68ThrfsTer?)
c.318_340+31del
COSMIC
17g.7675995_7676272delCA645589239TP53c.97_374del (p.Ser33ValfsTer23)
c.-21-1036_-21-759del (n.-21-1036_-21-759del)
c.96+110_96+387del (n.96+110_96+387del)
c.97_374del (p.Ser33AspfsTer16)
c.97_374del (p.Ser33ValfsTer?)
n.353_630del
c.-21_257del
c.97_340+30del
COSMIC
17g.7676011_7676058dupCA2245932646TP53c.313_360dup (p.Lys120_Ser121insGlySerTyrGlyPheArgLeuGlyPheLeuHisSerGlyThrAlaLys)
c.-21-820_-21-773dup (n.-21-820_-21-773dup)
c.96+326_96+373dup (n.96+326_96+373dup)
n.569_616dup
c.196_243dup (p.Lys81_Ser82insGlySerTyrGlyPheArgLeuGlyPheLeuHisSerGlyThrAlaLys)
c.313_340+16dup
ClinVar dbSNP
17g.7676029_7676041delinsAGAAGCCCAGACGCA2245932909TP53c.328_340delinsCGTCTGGGCTTCT (p.Arg110=)
c.-21-805_-21-793delinsCGTCTGGGCTTCT (n.-21-805_-21-793delinsCGTCTGGGCTTCT)
c.96+341_96+353delinsCGTCTGGGCTTCT (n.96+341_96+353delinsCGTCTGGGCTTCT)
n.584_596delinsCGTCTGGGCTTCT
c.211_223delinsCGTCTGGGCTTCT (p.Arg71=)
c.328_336delinsCGTCTGGGCTTCT
17g.7676029_7676047delinsAGAAGCCCAGACGGAAACCCA2245932911TP53c.322_340delinsGGTTTCCGTCTGGGCTTCT (p.Gly108=)
c.-21-811_-21-793delinsGGTTTCCGTCTGGGCTTCT (n.-21-811_-21-793delinsGGTTTCCGTCTGGGCTTCT)
c.96+335_96+353delinsGGTTTCCGTCTGGGCTTCT (n.96+335_96+353delinsGGTTTCCGTCTGGGCTTCT)
n.578_596delinsGGTTTCCGTCTGGGCTTCT
c.205_223delinsGGTTTCCGTCTGGGCTTCT (p.Gly69=)
c.322_336delinsGGTTTCCGTCTGGGCTTCT
17g.7676033_7676044delCA000115TP53c.328_339del (p.Arg110_Phe113del)
c.-21-805_-21-794del (n.-21-805_-21-794del)
c.96+341_96+352del (n.96+341_96+352del)
n.584_595del
c.211_222del (p.Arg71_Phe74del)
c.328_335del
ClinVar dbSNP
17g.7676031_7676048delCA10588673TP53c.322_339del (p.Gly108_Phe113del)
c.-21-811_-21-794del (n.-21-811_-21-794del)
c.96+335_96+352del (n.96+335_96+352del)
n.578_595del
c.205_222del (p.Gly69_Phe74del)
c.322_335del
ClinVar dbSNP
17g.7676033_7676045delinsGCCCAGACGGAAACA2245933005TP53c.324_336delinsTTTCCGTCTGGGC (p.Gly108=)
c.-21-809_-21-797delinsTTTCCGTCTGGGC (n.-21-809_-21-797delinsTTTCCGTCTGGGC)
c.96+337_96+349delinsTTTCCGTCTGGGC (n.96+337_96+349delinsTTTCCGTCTGGGC)
n.580_592delinsTTTCCGTCTGGGC
c.207_219delinsTTTCCGTCTGGGC (p.Gly69=)
c.324_334-2delinsTTTCCGTCTGGGC
17g.7676037_7676057delCA891842274TP53c.316_336del (p.Ser106_Gly112del)
c.-21-817_-21-797del (n.-21-817_-21-797del)
c.96+329_96+349del (n.96+329_96+349del)
n.572_592del
c.199_219del (p.Ser67_Gly73del)
c.316_334-2del
17g.7676036_7676047delCA1139665172TP53c.324_335del (p.Phe109_Gly112del)
c.-21-809_-21-798del (n.-21-809_-21-798del)
c.96+337_96+348del (n.96+337_96+348del)
n.580_591del
c.207_218del (p.Phe70_Gly73del)
c.324_334-3del
ClinVar dbSNP
17g.7676037_7676047dupCA2245933043TP53c.324_334dup (p.Gly112ValfsTer15)
c.-21-809_-21-799dup (n.-21-809_-21-799dup)
c.96+337_96+347dup (n.96+337_96+347dup)
n.580_590dup
c.207_217dup (p.Gly73ValfsTer15)
c.324_333+1dup
dbSNP
17g.7676035_7676061delCA645589272TP53c.308_334del (p.Tyr103_Gly112delinsCys)
c.-21-825_-21-799del (n.-21-825_-21-799del)
c.96+321_96+347del (n.96+321_96+347del)
n.564_590del
c.191_217del (p.Tyr64_Gly73delinsCys)
c.308_333+1del
COSMIC
17g.7676036_7676048delCA645589274TP53c.321_333del (p.Tyr107Ter)
c.-21-812_-21-800del (n.-21-812_-21-800del)
c.96+334_96+346del (n.96+334_96+346del)
n.577_589del
c.204_216del (p.Tyr68Ter)
c.321_333del (p.Gly108LeufsTer?)
COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676037_7676045delinsAGACGGAAACA2245933096TP53c.324_332delinsTTTCCGTCT (p.Gly108=)
c.-21-809_-21-801delinsTTTCCGTCT (n.-21-809_-21-801delinsTTTCCGTCT)
c.96+337_96+345delinsTTTCCGTCT (n.96+337_96+345delinsTTTCCGTCT)
n.580_588delinsTTTCCGTCT
c.207_215delinsTTTCCGTCT (p.Gly69=)
17g.7676038_7676045delCA645589276TP53c.325_332del (p.Phe109GlyfsTer?)
c.-21-808_-21-801del (n.-21-808_-21-801del)
c.96+338_96+345del (n.96+338_96+345del)
c.325_332del (p.Phe109GlyfsTer30)
n.581_588del
c.208_215del (p.Phe70GlyfsTer?)
c.325_332del (p.Phe109ValfsTer26)
COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676037_7676047delinsTGAATCA2497028965TP53c.322_332delinsATTCA (p.Gly108_Leu111delinsIleGln)
c.-21-811_-21-801delinsATTCA (n.-21-811_-21-801delinsATTCA)
c.96+335_96+345delinsATTCA (n.96+335_96+345delinsATTCA)
n.578_588delinsATTCA
c.205_215delinsATTCA (p.Gly69_Leu72delinsIleGln)
17g.7676039_7676041delCA645589278TP53c.329_331del (p.Arg110del)
c.-21-804_-21-802del (n.-21-804_-21-802del)
c.96+342_96+344del (n.96+342_96+344del)
n.585_587del
c.212_214del (p.Arg71del)
ClinVar COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676038_7676042delCA2499224978TP53c.327_331del (p.Arg110GlyfsTer?)
c.-21-806_-21-802del (n.-21-806_-21-802del)
c.96+340_96+344del (n.96+340_96+344del)
n.583_587del
c.210_214del (p.Arg71GlyfsTer?)
c.327_331del (p.Arg110ValfsTer26)
dbSNP
17g.7676040_7676043delCA645589277TP53c.328_331del (p.Arg110TrpfsTer12)
c.-21-805_-21-802del (n.-21-805_-21-802del)
c.96+341_96+344del (n.96+341_96+344del)
n.584_587del
c.211_214del (p.Arg71TrpfsTer12)
c.328_331del (p.Arg110CysfsTer?)
COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676038_7676045delinsTTTCA2245933138TP53c.324_331delinsAAA (p.Phe109AsnfsTer?)
c.-21-809_-21-802delinsAAA (n.-21-809_-21-802delinsAAA)
c.96+337_96+344delinsAAA (n.96+337_96+344delinsAAA)
n.580_587delinsAAA
c.207_214delinsAAA (p.Phe70AsnfsTer?)
c.324_331delinsAAA (p.Phe109AsnfsTer27)
ClinVar dbSNP
17g.7676041_7676090delCA645589279TP53c.282_331del (p.Ser95GlyfsTer?)
c.-21-851_-21-802del (n.-21-851_-21-802del)
c.96+295_96+344del (n.96+295_96+344del)
n.538_587del
c.165_214del (p.Ser56GlyfsTer?)
c.282_331del (p.Ser95ValfsTer26)
COSMIC
17g.7676041_7676046delCA645589280TP53c.325_330del (p.Phe109_Arg110del)
c.-21-808_-21-803del (n.-21-808_-21-803del)
c.96+338_96+343del (n.96+338_96+343del)
n.581_586del
c.208_213del (p.Phe70_Arg71del)
gnomAD v4 COSMIC
17g.7676040_7676050delCA645589281TP53c.320_330del (p.Tyr107SerfsTer?)
c.-21-813_-21-803del (n.-21-813_-21-803del)
c.96+333_96+343del (n.96+333_96+343del)
n.576_586del
c.203_213del (p.Tyr68SerfsTer?)
c.320_330del (p.Tyr107SerfsTer27)
COSMIC
17g.7676039_7676059delinsACGGAAACCGTAGCTGCCCTGCA2245933165TP53c.310_330delinsCAGGGCAGCTACGGTTTCCGT (p.Gln104=)
c.-21-823_-21-803delinsCAGGGCAGCTACGGTTTCCGT (n.-21-823_-21-803delinsCAGGGCAGCTACGGTTTCCGT)
c.96+323_96+343delinsCAGGGCAGCTACGGTTTCCGT (n.96+323_96+343delinsCAGGGCAGCTACGGTTTCCGT)
n.566_586delinsCAGGGCAGCTACGGTTTCCGT
c.193_213delinsCAGGGCAGCTACGGTTTCCGT (p.Gln65=)
17g.7676040_7676041delinsACA2695223131TP53c.328_329delinsT (p.Arg110PhefsTer13)
c.-21-805_-21-804delinsT (n.-21-805_-21-804delinsT)
c.96+341_96+342delinsT (n.96+341_96+342delinsT)
n.584_585delinsT
c.211_212delinsT (p.Arg71PhefsTer13)
c.328_329delinsT (p.Arg110PhefsTer?)
17g.7676040_7676041delinsCGCA2245933202TP53c.328_329delinsCG (p.Arg110=)
c.-21-805_-21-804delinsCG (n.-21-805_-21-804delinsCG)
c.96+341_96+342delinsCG (n.96+341_96+342delinsCG)
n.584_585delinsCG
c.211_212delinsCG (p.Arg71=)
17g.7676040_7676042delinsCGGCA2245933200TP53c.327_329delinsCCG (p.Phe109=)
c.-21-806_-21-804delinsCCG (n.-21-806_-21-804delinsCCG)
c.96+340_96+342delinsCCG (n.96+340_96+342delinsCCG)
n.583_585delinsCCG
c.210_212delinsCCG (p.Phe70=)
17g.7676040_7676044delinsCGGAACA2245933197TP53c.325_329delinsTTCCG (p.Phe109=)
c.-21-808_-21-804delinsTTCCG (n.-21-808_-21-804delinsTTCCG)
c.96+338_96+342delinsTTCCG (n.96+338_96+342delinsTTCCG)
n.581_585delinsTTCCG
c.208_212delinsTTCCG (p.Phe70=)
17g.7676040_7676045delinsCGGAAACA2245933198TP53c.324_329delinsTTTCCG (p.Gly108=)
c.-21-809_-21-804delinsTTTCCG (n.-21-809_-21-804delinsTTTCCG)
c.96+337_96+342delinsTTTCCG (n.96+337_96+342delinsTTTCCG)
n.580_585delinsTTTCCG
c.207_212delinsTTTCCG (p.Gly69=)
17g.7676045_7676046insGCGGAAACA2695223130TP53c.329_330insCTTTCCG (p.Leu111PhefsTer?)
c.-21-804_-21-803insCTTTCCG (n.-21-804_-21-803insCTTTCCG)
c.96+342_96+343insCTTTCCG (n.96+342_96+343insCTTTCCG)
n.585_586insCTTTCCG
c.212_213insCTTTCCG (p.Leu72PhefsTer?)
c.329_330insCTTTCCG (p.Leu111PhefsTer29)
17g.7676042_7676048dupCA645369686TP53c.323_329dup (p.Leu111PhefsTer?)
c.-21-810_-21-804dup (n.-21-810_-21-804dup)
c.96+336_96+342dup (n.96+336_96+342dup)
n.579_585dup
c.206_212dup (p.Leu72PhefsTer?)
c.323_329dup (p.Leu111PhefsTer29)
ClinVar dbSNP
17g.7676042_7676048delCA2739265611TP53c.323_329del (p.Gly108ValfsTer13)
c.-21-810_-21-804del (n.-21-810_-21-804del)
c.96+336_96+342del (n.96+336_96+342del)
n.579_585del
c.206_212del (p.Gly69ValfsTer13)
c.323_329del (p.Gly108ValfsTer?)
ClinVar
17g.7676040_7676059delCA658656635TP53c.310_329del (p.Gln104SerfsTer?)
c.-21-823_-21-804del (n.-21-823_-21-804del)
c.96+323_96+342del (n.96+323_96+342del)
n.566_585del
c.193_212del (p.Gln65SerfsTer?)
c.310_329del (p.Gln104SerfsTer27)
ClinVar dbSNP
17g.7676041G>ACA000119TP53c.328C>T (p.Arg110Cys)
c.-21-805C>T (n.-21-805C>T)
c.96+341C>T (n.96+341C>T)
n.584C>T
c.211C>T (p.Arg71Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676041G>CCA397844579TP53c.328C>G (p.Arg110Gly)
c.-21-805C>G (n.-21-805C>G)
c.96+341C>G (n.96+341C>G)
n.584C>G
c.211C>G (p.Arg71Gly)
ClinVar dbSNP
17g.7676041G=CA2245933264TP53c.328C= (p.Arg110=)
c.-21-805C= (n.-21-805C=)
c.96+341C= (n.96+341C=)
n.584C=
c.211C= (p.Arg71=)
17g.7676041G>TCA000117TP53c.328C>A (p.Arg110Ser)
c.-21-805C>A (n.-21-805C>A)
c.96+341C>A (n.96+341C>A)
n.584C>A
c.211C>A (p.Arg71Ser)
ClinVar dbSNP COSMIC
17g.7676041_7676042delCA16620636TP53c.327_328del (p.Phe109LeufsTer?)
c.-21-806_-21-805del (n.-21-806_-21-805del)
c.96+340_96+341del (n.96+340_96+341del)
n.583_584del
c.210_211del (p.Phe70LeufsTer?)
c.327_328del (p.Phe109LeufsTer28)
ClinVar dbSNP
17g.7676041_7676042delinsAACA645589283TP53c.327_328delinsTT (p.Arg110Cys)
c.-21-806_-21-805delinsTT (n.-21-806_-21-805delinsTT)
c.96+340_96+341delinsTT (n.96+340_96+341delinsTT)
n.583_584delinsTT
c.210_211delinsTT (p.Arg71Cys)
COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7676042_7676043insTGGCA891842276TP53c.328_329insACC (p.Phe109_Arg110insHis)
c.-21-805_-21-804insACC (n.-21-805_-21-804insACC)
c.96+341_96+342insACC (n.96+341_96+342insACC)
n.584_585insACC
c.211_212insACC (p.Phe70_Arg71insHis)

Number of alleles fetched