Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FUT1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750423:48750423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.859G>A
AA Mutation p.Glu287Lys(p.E287K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750717:48750717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.565G>A
AA Mutation p.Asp189Asn(p.D189N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750563:48750563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.719C>T
AA Mutation p.Ala240Val(p.A240V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750821:48750821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.461A>G
AA Mutation p.Tyr154Cys(p.Y154C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750818:48750818(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.464C>T
AA Mutation p.Ala155Val(p.A155V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750648:48750648(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771713990
CDS Mutation c.634C>T
AA Mutation p.Arg212Cys(p.R212C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750513:48750513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.769G>A
AA Mutation p.Val257Ile(p.V257I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750962:48750962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.320G>A
AA Mutation p.Gly107Asp(p.G107D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750443:48750443(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748679094
CDS Mutation c.839C>T
AA Mutation p.Thr280Met(p.T280M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750330:48750330(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.952G>A
AA Mutation p.Ala318Thr(p.A318T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750555:48750555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.727C>T
AA Mutation p.Arg243Trp(p.R243W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48751087:48751087(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763594230
CDS Mutation c.195C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750412:48750412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.870G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000310160
Start 48750829:48750829(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.453G>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> FUT1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310160
Start 48750432:48750432(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557041594
CDS Mutation c.850G>A
AA Mutation p.Asp284Asn(p.D284N)
Mutation Classification Missense_Mutation
Feature Type Transcript