Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADAMTS18

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77319913:77319913(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2468G>A
AA Mutation p.Arg823His(p.R823H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77291368:77291368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3300G>T
AA Mutation p.Lys1100Asn(p.K1100N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77356058:77356058(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1342G>A
AA Mutation p.Gly448Arg(p.G448R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77363840:77363840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1018G>A
AA Mutation p.Val340Met(p.V340M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77341736:77341736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1678G>A
AA Mutation p.Ala560Thr(p.A560T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77362215:77362215(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1106G>A
AA Mutation p.Cys369Tyr(p.C369Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77367449:77367449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.770G>A
AA Mutation p.Arg257His(p.R257H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77295046:77295046(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2883G>T
AA Mutation p.Lys961Asn(p.K961N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77319914:77319914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2467C>T
AA Mutation p.Arg823Cys(p.R823C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77353854:77353854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1493C>A
AA Mutation p.Pro498His(p.P498H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000282849
Start 77293078:77293078(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765403489
CDS Mutation c.3187G>A
AA Mutation p.Glu1063Lys(p.E1063K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77431522:77431522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268G>A
AA Mutation p.Ala90Thr(p.A90T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77319997:77319997(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2384G>A
AA Mutation p.Ser795Asn(p.S795N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77291306:77291306(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3362A>G
AA Mutation p.Tyr1121Cys(p.Y1121C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77431356:77431356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434A>T
AA Mutation p.Tyr145Phe(p.Y145F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77359364:77359364(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1276A>T
AA Mutation p.Thr426Ser(p.T426S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77364249:77364249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.911A>G
AA Mutation p.Lys304Arg(p.K304R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77362176:77362176(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368783738
CDS Mutation c.1145G>A
AA Mutation p.Arg382Lys(p.R382K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77367528:77367528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.691C>A
AA Mutation p.His231Asn(p.H231N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77284038:77284038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3584G>C
AA Mutation p.Cys1195Ser(p.C1195S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77325898:77325898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2000T>G
AA Mutation p.Phe667Cys(p.F667C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77367445:77367445(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.774G>T
AA Mutation p.Lys258Asn(p.K258N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77367671:77367671(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.548A>C
AA Mutation p.Gln183Pro(p.Q183P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77341727:77341727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1687G>A
AA Mutation p.Gly563Arg(p.G563R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77293239:77293239(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142167857
CDS Mutation c.3026G>A
AA Mutation p.Arg1009Gln(p.R1009Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77294936:77294936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2993G>A
AA Mutation p.Gly998Glu(p.G998E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77325949:77325949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1949T>G
AA Mutation p.Phe650Cys(p.F650C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77335898:77335898(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1717C>T
AA Mutation p.Arg573Trp(p.R573W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77363819:77363819(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113981106
CDS Mutation c.1039C>A
AA Mutation p.Leu347Ile(p.L347I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77362176:77362176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1145G>T
AA Mutation p.Arg382Ile(p.R382I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77326008:77326008(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1890T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77431523:77431523(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777631533
CDS Mutation c.267G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77431520:77431520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142460481
CDS Mutation c.270G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77431448:77431448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77289340:77289340(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3474A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000282849
Start 77325948:77325948(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1950delT
AA Mutation p.Arg651GlyfsTer51(p.R651Gfs*51)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000282849
Start 77300320:77300320(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2617delA
AA Mutation p.Arg873AspfsTer22(p.R873Dfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 38
Mutation Consequence stop_gained
Transcription ID ENST00000282849
Start 77367577:77367577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.642C>A
AA Mutation p.Tyr214Ter(p.Y214*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence stop_gained
Transcription ID ENST00000282849
Start 77320007:77320007(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747773771
CDS Mutation c.2374C>T
AA Mutation p.Arg792Ter(p.R792*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence stop_gained
Transcription ID ENST00000282849
Start 77284058:77284058(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3564C>A
AA Mutation p.Cys1188Ter(p.C1188*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence stop_gained
Transcription ID ENST00000282849
Start 77293126:77293126(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3139C>T
AA Mutation p.Arg1047Ter(p.R1047*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ADAMTS18

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77367596:77367596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623A>T
AA Mutation p.Glu208Val(p.E208V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77320006:77320006(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774713566
CDS Mutation c.2375G>A
AA Mutation p.Arg792Gln(p.R792Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77335859:77335859(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769577910
CDS Mutation c.1756C>T
AA Mutation p.Arg586Trp(p.R586W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77284002:77284002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3620A>C
AA Mutation p.Lys1207Thr(p.K1207T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77293107:77293107(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs534278374
CDS Mutation c.3158G>A
AA Mutation p.Arg1053Gln(p.R1053Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77293218:77293218(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3047T>C
AA Mutation p.Leu1016Pro(p.L1016P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77319938:77319938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2443G>A
AA Mutation p.Ala815Thr(p.A815T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77353824:77353824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1523A>C
AA Mutation p.Asp508Ala(p.D508A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77356070:77356070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1330A>C
AA Mutation p.Met444Leu(p.M444L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77321092:77321092(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2274G>T
AA Mutation p.Gln758His(p.Q758H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000282849
Start 77319883:77319883(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147816593
CDS Mutation c.2498C>T
AA Mutation p.Ala833Val(p.A833V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77293094:77293094(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187998780
CDS Mutation c.3171C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000282849
Start 77431520:77431520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142460481
CDS Mutation c.270G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000282849
Start 77367483:77367483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.736C>T
AA Mutation p.Arg246Ter(p.R246*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript