Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC39A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33203547:33203547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33202403:33202403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775G>A
AA Mutation	p.Gly259Arg(p.G259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33202385:33202385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745393541
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33203062:33203062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093G>A
AA Mutation	p.Gly365Arg(p.G365R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33203563:33203563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160C>T
AA Mutation	p.Thr387Ile(p.T387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374675
Start	33202657:33202657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374675
Start	33202381:33202381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374675
Start	33202597:33202597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374675
Start	33201260:33201260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.19delG
AA Mutation	p.Ala7ProfsTer10(p.A7Pfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374675
Start	33201781:33201781(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.453delT
AA Mutation	p.Phe151LeufsTer87(p.F151Lfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33203584:33203584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181G>T
AA Mutation	p.Gly394Val(p.G394V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374675
Start	33203547:33203547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript