Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC6A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116458919:116458919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893A>C
AA Mutation	p.Glu631Asp(p.E631D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116437901:116437901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Val54Met(p.V54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116446847:116446847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896C>A
AA Mutation	p.Ala299Asp(p.A299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116446796:116446796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371749747
CDS Mutation	c.845G>A
AA Mutation	p.Arg282Gln(p.R282Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116444926:116444926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782086169
CDS Mutation	c.665C>T
AA Mutation	p.Ala222Val(p.A222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116455041:116455041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1469C>T
AA Mutation	p.Ala490Val(p.A490V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116451458:116451458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947C>A
AA Mutation	p.Ala316Asp(p.A316D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116453121:116453121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1264G>A
AA Mutation	p.Asp422Asn(p.D422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000598581
Start	116458884:116458884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1858G>T
AA Mutation	p.Asp620Tyr(p.D620Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript