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Mutation
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Colon Cancer: Gene >> CYSLTR1
Mutation ID
1
Mutation Consequence
missense_variant
Transcription ID
ENST00000373304
Start
78273155:78273155(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.592T>G
AA Mutation
p.Phe198Val(p.F198V)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
2
Mutation Consequence
missense_variant
Transcription ID
ENST00000373304
Start
78273483:78273483(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.264T>G
AA Mutation
p.Ile88Met(p.I88M)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
3
Mutation Consequence
missense_variant
Transcription ID
ENST00000373304
Start
78272859:78272859(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.888C>A
AA Mutation
p.Phe296Leu(p.F296L)
Mutation Classification
Missense_Mutation
Feature Type
Transcript
Mutation ID
4
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000373304
Start
78273057:78273057(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
rs138981290
CDS Mutation
c.690G>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
5
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000373304
Start
78273612:78273612(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.135C>G
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
6
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000373304
Start
78273441:78273441(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.306T>G
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
7
Mutation Consequence
synonymous_variant
Transcription ID
ENST00000373304
Start
78272949:78272949(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
novel
CDS Mutation
c.798C>A
Mutation Classification
Silent
Feature Type
Transcript
Mutation ID
8
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000373304
Start
78273058:78273058(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.689delA
AA Mutation
p.Lys230ArgfsTer3(p.K230Rfs*3)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Mutation ID
9
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000373304
Start
78273090:78273090(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
null
CDS Mutation
c.657delA
AA Mutation
p.Lys219AsnfsTer3(p.K219Nfs*3)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Mutation ID
10
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000373304
Start
78273076:78273076(version: GRCh38)
Mutation Type
DEL
dbSNP_RS
novel
CDS Mutation
c.671delA
AA Mutation
p.Asn224IlefsTer9(p.N224Ifs*9)
Mutation Classification
Frame_Shift_Del
Feature Type
Transcript
Mutation ID
11
Mutation Consequence
stop_gained
Transcription ID
ENST00000373304
Start
78273050:78273050(version: GRCh38)
Mutation Type
SNP
dbSNP_RS
null
CDS Mutation
c.697G>T
AA Mutation
p.Gly233Ter(p.G233*)
Mutation Classification
Nonsense_Mutation
Feature Type
Transcript
Mutation ID
12
Mutation Consequence
frameshift_variant
Transcription ID
ENST00000373304
Start
78273075:78273076(version: GRCh38)
Mutation Type
INS
dbSNP_RS
null
CDS Mutation
c.670_671dupAA
AA Mutation
p.Asn224LysfsTer10(p.N224Kfs*10)
Mutation Classification
Frame_Shift_Ins
Feature Type
Transcript
Rectum Cancer: Gene >> CYSLTR1
No Mutation Annotation!