Colon Cancer: Gene >> PCYT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24562300:24562300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103A>G
AA Mutation	p.Glu368Gly(p.E368G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24590091:24590091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Cys(p.R140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24579393:24579393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Cys(p.R211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24590081:24590081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428A>G
AA Mutation	p.Asp143Gly(p.D143G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24590090:24590090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379144
Start	24590023:24590023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486G>T
AA Mutation	p.Lys162Asn(p.K162N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379144
Start	24562472:24562472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PCYT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379145
Start	24672582:24672582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51A>C
AA Mutation	p.Gln17His(p.Q17H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24607835:24607835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Asp82Asn(p.D82N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379144
Start	24590085:24590085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Val142Ile(p.V142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379144
Start	24562296:24562296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript