Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IDE

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92463898:92463898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2594C>T
AA Mutation p.Ala865Val(p.A865V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92483307:92483307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1687C>G
AA Mutation p.Gln563Glu(p.Q563E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92508125:92508125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1141G>A
AA Mutation p.Glu381Lys(p.E381K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92454506:92454506(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2998C>T
AA Mutation p.Arg1000Cys(p.R1000C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92465748:92465748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2416A>G
AA Mutation p.Met806Val(p.M806V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92463785:92463785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2707G>A
AA Mutation p.Glu903Lys(p.E903K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92468941:92468941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2258C>T
AA Mutation p.Ala753Val(p.A753V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92463847:92463847(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2645T>C
AA Mutation p.Phe882Ser(p.F882S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92510145:92510145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.802A>T
AA Mutation p.Thr268Ser(p.T268S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000265986
Start 92508840:92508840(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751705951
CDS Mutation c.948A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000265986
Start 92531887:92531887(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749046548
CDS Mutation c.522C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000265986
Start 92465788:92465788(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2376G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000265986
Start 92514978:92514978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.726G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000265986
Start 92454489:92454489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3015T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000265986
Start 92534722:92534722(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.347delT
AA Mutation p.Leu116TrpfsTer43(p.L116Wfs*43)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000265986
Start 92483288:92483288(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs771790236
CDS Mutation c.1706delT
AA Mutation p.Leu569CysfsTer45(p.L569Cfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000265986
Start 92474955:92474955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2002C>T
AA Mutation p.Arg668Ter(p.R668*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000265986
Start 92508146:92508147(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1119dupT
AA Mutation p.Ile374TyrfsTer3(p.I374Yfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000265986
Start 92483287:92483288(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1706dupT
AA Mutation p.Leu569PhefsTer9(p.L569Ffs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> IDE

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92454497:92454497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3007C>A
AA Mutation p.Pro1003Thr(p.P1003T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000265986
Start 92531916:92531916(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.493T>C
AA Mutation p.Phe165Leu(p.F165L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265986
Start 92534712:92534712(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357G>T
AA Mutation p.Lys119Asn(p.K119N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000265986
Start 92537456:92537456(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751312151
CDS Mutation c.193C>T
AA Mutation p.Arg65Ter(p.R65*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript