Colon Cancer: Gene >> SLC52A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144359799:144359799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144360105:144360105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144883729
CDS Mutation	c.613G>A
AA Mutation	p.Val205Ile(p.V205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144360228:144360228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.736G>A
AA Mutation	p.Glu246Lys(p.E246K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144360616:144360616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028C>T
AA Mutation	p.Ser343Phe(p.S343F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144359727:144359727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235G>A
AA Mutation	p.Val79Ile(p.V79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144360845:144360845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168A>G
AA Mutation	p.Lys390Glu(p.K390E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329994
Start	144360359:144360359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329994
Start	144360653:144360653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200618841
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC52A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144359938:144359938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446T>C
AA Mutation	p.Leu149Pro(p.L149P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329994
Start	144360932:144360932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397514658
CDS Mutation	c.1255G>A
AA Mutation	p.Gly419Ser(p.G419S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript