Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SRSF1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258962
Start 58006493:58006493(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.229T>A
AA Mutation p.Tyr77Asn(p.Y77N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258962
Start 58005948:58005948(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.405G>T
AA Mutation p.Gln135His(p.Q135H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000258962
Start 58005939:58005939(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414G>T
AA Mutation p.Lys138Asn(p.K138N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000258962
Start 58007105:58007105(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.33A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000258962
Start 58005909:58005909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.444T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000258962
Start 58006404:58006404(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000258962
Start 58005950:58005950(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.403C>T
AA Mutation p.Gln135Ter(p.Q135*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000258962
Start 58005601:58005601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.553-1G>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> SRSF1

No Mutation Annotation!