Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NTS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256010
Start	85882324:85882324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462G>T
AA Mutation	p.Glu154Asp(p.E154D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256010
Start	85876677:85876677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148367587
CDS Mutation	c.111C>A
AA Mutation	p.Phe37Leu(p.F37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256010
Start	85882285:85882285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78763072
CDS Mutation	c.423G>T
AA Mutation	p.Lys141Asn(p.K141N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NTS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256010
Start	85882358:85882358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>T
AA Mutation	p.Asp166Tyr(p.D166Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256010
Start	85882356:85882356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494G>T
AA Mutation	p.Arg165Ile(p.R165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript