Primary Site >> Colorectal Cancer

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!