Colon Cancer: Gene >> SLC52A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254853
Start	5033555:5033555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>A
AA Mutation	p.Ala312Thr(p.A312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254853
Start	5033757:5033757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732G>T
AA Mutation	p.Glu244Asp(p.E244D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254853
Start	5033614:5033614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875T>C
AA Mutation	p.Val292Ala(p.V292A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254853
Start	5033274:5033274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>T
AA Mutation	p.Gly374Val(p.G374V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254853
Start	5033891:5033891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000254853
Start	5033335:5033335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1060delG
AA Mutation	p.Ala354ProfsTer3(p.A354Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC52A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254853
Start	5034600:5034600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>T
AA Mutation	p.Ala3Ser(p.A3S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254853
Start	5033739:5033739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750T>G
Mutation Classification	Silent
Feature Type	Transcript