Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> WNT8B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343737
Start 100482411:100482411(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.651G>C
AA Mutation p.Lys217Asn(p.K217N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000343737
Start 100480006:100480006(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556948230
CDS Mutation c.235C>T
AA Mutation p.Arg79Cys(p.R79C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000343737
Start 100482412:100482412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.652G>A
AA Mutation p.Val218Met(p.V218M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000343737
Start 100479928:100479928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>A
AA Mutation p.Glu53Lys(p.E53K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000343737
Start 100482423:100482423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.663G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000343737
Start 100482585:100482585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.825C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> WNT8B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343737
Start 100463188:100463188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.20C>A
AA Mutation p.Ser7Tyr(p.S7Y)
Mutation Classification Missense_Mutation
Feature Type Transcript