Colon Cancer: Gene >> SLC39A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56231539:56231539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>T
AA Mutation	p.Ala89Ser(p.A89S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56236623:56236623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084C>T
AA Mutation	p.Pro362Ser(p.P362S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56235632:56235632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756666376
CDS Mutation	c.877G>A
AA Mutation	p.Gly293Arg(p.G293R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56235674:56235674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919C>T
AA Mutation	p.Leu307Phe(p.L307F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56236456:56236456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1006A>G
AA Mutation	p.Ser336Gly(p.S336G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56237154:56237154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>A
AA Mutation	p.Asp431Glu(p.D431E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56237005:56237005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750169649
CDS Mutation	c.1282G>A
AA Mutation	p.Glu428Lys(p.E428K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56236426:56236426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374210703
CDS Mutation	c.976G>A
AA Mutation	p.Glu326Lys(p.E326K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56232851:56232851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450G>T
AA Mutation	p.Leu150Phe(p.L150F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56231524:56231524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199681035
CDS Mutation	c.250C>T
AA Mutation	p.Arg84Trp(p.R84W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266980
Start	56231541:56231541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266980
Start	56236690:56236690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766647859
CDS Mutation	c.1151C>T
AA Mutation	p.Thr384Met(p.T384M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266980
Start	56237713:56237713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150715610
CDS Mutation	c.1605C>T
Mutation Classification	Silent
Feature Type	Transcript