Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ADCY5

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291124:123291124(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3316G>T
AA Mutation p.Asp1106Tyr(p.D1106Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123300145:123300145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775356872
CDS Mutation c.2875G>A
AA Mutation p.Asp959Asn(p.D959N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291295:123291295(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3145G>A
AA Mutation p.Ala1049Thr(p.A1049T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123319718:123319718(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2212C>T
AA Mutation p.Arg738Cys(p.R738C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123447544:123447544(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1002C>A
AA Mutation p.Phe334Leu(p.F334L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123319766:123319766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2164C>T
AA Mutation p.Arg722Cys(p.R722C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123325451:123325451(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1959G>T
AA Mutation p.Lys653Asn(p.K653N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123447579:123447579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.967C>T
AA Mutation p.Arg323Cys(p.R323C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123325428:123325428(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771319042
CDS Mutation c.1982G>A
AA Mutation p.Arg661His(p.R661H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123447513:123447513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1033G>A
AA Mutation p.Val345Met(p.V345M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291274:123291274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3166G>A
AA Mutation p.Glu1056Lys(p.E1056K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123289792:123289792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3490T>C
AA Mutation p.Tyr1164His(p.Y1164H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123332587:123332587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1495G>A
AA Mutation p.Ala499Thr(p.A499T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123300162:123300162(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372170924
CDS Mutation c.2858C>T
AA Mutation p.Thr953Met(p.T953M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123352464:123352464(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs864309483
CDS Mutation c.1252C>T
AA Mutation p.Arg418Trp(p.R418W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291268:123291268(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759519156
CDS Mutation c.3172C>T
AA Mutation p.Arg1058Cys(p.R1058C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123447638:123447638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757908717
CDS Mutation c.908A>G
AA Mutation p.Tyr303Cys(p.Y303C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291307:123291307(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3133C>T
AA Mutation p.Pro1045Ser(p.P1045S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123318095:123318095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766054571
CDS Mutation c.2279G>A
AA Mutation p.Arg760Gln(p.R760Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123291270:123291270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139641136
CDS Mutation c.3170G>A
AA Mutation p.Arg1057Gln(p.R1057Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123328656:123328656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1793G>A
AA Mutation p.Gly598Asp(p.G598D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123347816:123347816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1372C>A
AA Mutation p.His458Asn(p.H458N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123303128:123303128(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529379333
CDS Mutation c.2651C>T
AA Mutation p.Ser884Leu(p.S884L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123303106:123303106(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776048153
CDS Mutation c.2673C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123300161:123300161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2859G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123296135:123296135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142086014
CDS Mutation c.3012C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123447673:123447673(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.873C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123330969:123330969(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148753023
CDS Mutation c.1566C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123447949:123447949(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.597C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123296207:123296207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2940T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123300125:123300125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2895C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123304103:123304103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2523C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000462833
Start 123327729:123327730(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1835dupA
AA Mutation p.Asn612LysfsTer66(p.N612Kfs*66)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000462833
Start 123304169:123304170(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2456dupC
AA Mutation p.Leu820ThrfsTer74(p.L820Tfs*74)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> ADCY5

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123320762:123320762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2098G>T
AA Mutation p.Asp700Tyr(p.D700Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000462833
Start 123304083:123304083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150642009
CDS Mutation c.2543C>T
AA Mutation p.Ala848Val(p.A848V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123291203:123291203(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3237C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123303163:123303163(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766902305
CDS Mutation c.2616C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000462833
Start 123291227:123291227(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs111603078
CDS Mutation c.3213G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000462833
Start 123325459:123325459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1951G>T
AA Mutation p.Glu651Ter(p.E651*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript