Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CD226

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000280200
Start 69895806:69895806(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143019865
CDS Mutation c.622G>A
AA Mutation p.Val208Ile(p.V208I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000280200
Start 69895990:69895990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438G>T
AA Mutation p.Lys146Asn(p.K146N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895750:69895750(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.678C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895747:69895747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139259703
CDS Mutation c.681C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895903:69895903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.525C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895882:69895882(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895777:69895777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs207476919
CDS Mutation c.651G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000280200
Start 69947390:69947390(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.17T>G
AA Mutation p.Leu6Ter(p.L6*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> CD226

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000280200
Start 69895734:69895734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694G>A
AA Mutation p.Glu232Lys(p.E232K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000280200
Start 69895927:69895927(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.501G>A
Mutation Classification Silent
Feature Type Transcript