Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DSE

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116426689:116426689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532C>A
AA Mutation p.Leu178Ile(p.L178I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436297:116436297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1829G>T
AA Mutation p.Arg610Ile(p.R610I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116435727:116435727(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1259G>A
AA Mutation p.Gly420Glu(p.G420E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436615:116436615(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs549153887
CDS Mutation c.2147G>A
AA Mutation p.Arg716His(p.R716H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436829:116436829(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2361G>T
AA Mutation p.Glu787Asp(p.E787D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436053:116436053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1585G>A
AA Mutation p.Glu529Lys(p.E529K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116431101:116431101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.818T>C
AA Mutation p.Met273Thr(p.M273T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116426689:116426689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532C>T
AA Mutation p.Leu178Phe(p.L178F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436775:116436775(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2307C>A
AA Mutation p.Ser769Arg(p.S769R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116437081:116437081(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2613A>C
AA Mutation p.Lys871Asn(p.K871N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116436124:116436124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1656G>T
AA Mutation p.Lys552Asn(p.K552N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116435816:116435816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1348C>T
AA Mutation p.His450Tyr(p.H450Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116399600:116399600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.350C>A
AA Mutation p.Pro117His(p.P117H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116426607:116426607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773416085
CDS Mutation c.450G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116436052:116436052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1584A>G
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> DSE

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116399288:116399288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.38T>C
AA Mutation p.Phe13Ser(p.F13S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116426708:116426708(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.551C>A
AA Mutation p.Ala184Asp(p.A184D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000331677
Start 116431179:116431179(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.896G>T
AA Mutation p.Arg299Ile(p.R299I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000331677
Start 116399325:116399325(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752936676
CDS Mutation c.75C>T
Mutation Classification Silent
Feature Type Transcript