Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> G6PC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253801
Start 42907615:42907615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.433A>G
AA Mutation p.Thr145Ala(p.T145A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253801
Start 42911344:42911344(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149486847
CDS Mutation c.992C>T
AA Mutation p.Ala331Val(p.A331V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000253801
Start 42911414:42911414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1062G>T
AA Mutation p.Lys354Asn(p.K354N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000253801
Start 42900891:42900891(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.15G>T
AA Mutation p.Met5Ile(p.M5I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000253801
Start 42911045:42911045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.693T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000253801
Start 42911315:42911315(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.963C>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> G6PC

Mutation ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000253801
Start 42911306:42911306(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372612424
CDS Mutation c.954C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000253801
Start 42911087:42911087(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750147891
CDS Mutation c.735C>T
Mutation Classification Silent
Feature Type Transcript