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Primary Site >> Colorectal Cancer
Overview
Mutation
Expression
Methylation
Prognosis
Literature
Timeline
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!