Colon Cancer: Gene >> SLC2A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373371
Start	127403681:127403681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767054400
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Trp(p.R249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373371
Start	127404977:127404977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136G>A
AA Mutation	p.Cys379Tyr(p.C379Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373371
Start	127402647:127402647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372901354
CDS Mutation	c.617C>T
AA Mutation	p.Pro206Leu(p.P206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373371
Start	127403766:127403766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830T>A
AA Mutation	p.Phe277Tyr(p.F277Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373371
Start	127402697:127402697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571624823
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Trp(p.R223W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373371
Start	127403755:127403755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372199931
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000373371
Start	127407248:127407248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373371
Start	127398057:127398057(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.377delG
AA Mutation	p.Gly126AlafsTer14(p.G126Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373371
Start	127402601:127402601(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.576delC
AA Mutation	p.Ser193ProfsTer18(p.S193Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373371
Start	127402732:127402732(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753406313
CDS Mutation	c.708delC
AA Mutation	p.Ile237SerfsTer27(p.I237Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373371
Start	127405538:127405538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34424745
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373371
Start	127402731:127402732(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs199808560
CDS Mutation	c.708dupC
AA Mutation	p.Ile237HisfsTer4(p.I237Hfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript