Colon Cancer: Gene >> SLC29A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66363516:66363516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>T
AA Mutation	p.Gly431Cys(p.G431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66368579:66368579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66368585:66368585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>T
AA Mutation	p.Gly168Cys(p.G168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66368557:66368557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530C>A
AA Mutation	p.Ala177Asp(p.A177D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66363446:66363446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140572979
CDS Mutation	c.1361C>T
AA Mutation	p.Ala454Val(p.A454V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66366218:66366218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771598411
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66369161:66369161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357440
Start	66369428:66369428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC29A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357440
Start	66363513:66363513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774663200
CDS Mutation	c.1294G>A
AA Mutation	p.Ala432Thr(p.A432T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357440
Start	66369424:66369424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220C>T
Mutation Classification	Silent
Feature Type	Transcript