Colon Cancer: Gene >> SLC2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426263
Start	42931169:42931169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201815571
CDS Mutation	c.152G>A
AA Mutation	p.Arg51His(p.R51H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426263
Start	42929765:42929765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139412383
CDS Mutation	c.695G>A
AA Mutation	p.Arg232His(p.R232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000426263
Start	42929766:42929766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387907313
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000426263
Start	42927108:42927108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1412delG
AA Mutation	p.Gly471GlufsTer37(p.G471Efs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000426263
Start	42929018:42929018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80359826
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Ter(p.R330*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426263
Start	42929215:42929215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749426767
CDS Mutation	c.967G>A
AA Mutation	p.Val323Met(p.V323M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript