Colon Cancer: Gene >> SLC39A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269740
Start	2733326:2733326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775552929
CDS Mutation	c.370G>A
AA Mutation	p.Gly124Arg(p.G124R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269740
Start	2732783:2732783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200442678
CDS Mutation	c.913G>A
AA Mutation	p.Val305Ile(p.V305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269740
Start	2733141:2733141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269740
Start	2733192:2733192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569363399
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269740
Start	2733357:2733357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374448625
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269740
Start	2733262:2733262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770897898
CDS Mutation	c.434C>T
AA Mutation	p.Ala145Val(p.A145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript