Colon Cancer: Gene >> SLC2A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284361:7284361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202200041
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284494:7284494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768365925
CDS Mutation	c.737G>A
AA Mutation	p.Arg246His(p.R246H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7286460:7286460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766922260
CDS Mutation	c.1361C>T
AA Mutation	p.Ala454Val(p.A454V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284509:7284509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752C>T
AA Mutation	p.Ala251Val(p.A251V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7286580:7286580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481T>C
AA Mutation	p.Val494Ala(p.V494A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284009:7284009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>A
AA Mutation	p.Glu162Lys(p.E162K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284601:7284601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770842692
CDS Mutation	c.844C>T
AA Mutation	p.Arg282Cys(p.R282C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7283746:7283746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284335:7284335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780097545
CDS Mutation	c.683G>A
AA Mutation	p.Arg228His(p.R228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317370
Start	7284047:7284047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317370
Start	7284324:7284324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72556546
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7284859:7284859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940T>C
AA Mutation	p.Phe314Leu(p.F314L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317370
Start	7285797:7285797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215C>A
AA Mutation	p.Phe405Leu(p.F405L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317370
Start	7284849:7284849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541494158
CDS Mutation	c.930G>A
Mutation Classification	Silent
Feature Type	Transcript