Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TLR2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703202:153703202(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.295C>A
AA Mutation p.Leu99Met(p.L99M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703604:153703604(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.697G>T
AA Mutation p.Asp233Tyr(p.D233Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703256:153703256(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.349T>G
AA Mutation p.Ser117Ala(p.S117A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703928:153703928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1021A>T
AA Mutation p.Ile341Phe(p.I341F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704601:153704601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1694A>G
AA Mutation p.Asp565Gly(p.D565G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704104:153704104(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1197G>T
AA Mutation p.Leu399Phe(p.L399F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153702975:153702975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.68C>T
AA Mutation p.Ser23Phe(p.S23F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000260010
Start 153703393:153703393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.486C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000260010
Start 153704617:153704617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778957670
CDS Mutation c.1710G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000260010
Start 153705217:153705217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2310G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000260010
Start 153704348:153704348(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1441G>T
AA Mutation p.Glu481Ter(p.E481*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000260010
Start 153703620:153703621(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.718dupT
AA Mutation p.Ser240PhefsTer7(p.S240Ffs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000260010
Start 153705130:153705131(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2229dupA
AA Mutation p.Ala744SerfsTer47(p.A744Sfs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TLR2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704855:153704855(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745621022
CDS Mutation c.1948C>T
AA Mutation p.Arg650Trp(p.R650W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703407:153703407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.500G>T
AA Mutation p.Arg167Ile(p.R167I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703032:153703032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.125C>A
AA Mutation p.Ser42Tyr(p.S42Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153703873:153703873(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.966T>G
AA Mutation p.Phe322Leu(p.F322L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704157:153704157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1250A>G
AA Mutation p.Asn417Ser(p.N417S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704989:153704989(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374310145
CDS Mutation c.2082A>C
AA Mutation p.Glu694Asp(p.E694D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153704218:153704218(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1311G>T
AA Mutation p.Lys437Asn(p.K437N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000260010
Start 153705150:153705150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370330063
CDS Mutation c.2243G>A
AA Mutation p.Arg748His(p.R748H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000260010
Start 153703543:153703543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746216810
CDS Mutation c.636A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000260010
Start 153703754:153703754(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.847G>T
AA Mutation p.Glu283Ter(p.E283*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript