Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SYCE1L

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378644
Start 77199459:77199459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8G>C
AA Mutation p.Gly3Ala(p.G3A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000378644
Start 77212369:77212369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.581G>A
AA Mutation p.Gly194Glu(p.G194E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378644
Start 77206495:77206495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.116A>G
AA Mutation p.Gln39Arg(p.Q39R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000378644
Start 77209460:77209460(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374126372
CDS Mutation c.348C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence splice_donor_variant
Transcription ID ENST00000378644
Start 77206502:77206502(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.121+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> SYCE1L

No Mutation Annotation!