Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC6A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153691373:153691373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464G>A
AA Mutation	p.Gly155Asp(p.G155D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153691406:153691406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Thr166Met(p.T166M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153695194:153695194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373570632
CDS Mutation	c.1888G>A
AA Mutation	p.Val630Met(p.V630M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153693925:153693925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374163604
CDS Mutation	c.1162G>A
AA Mutation	p.Ala388Thr(p.A388T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153693096:153693096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782802482
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253122
Start	153693558:153693558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153693362:153693362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012T>C
AA Mutation	p.Tyr338His(p.Y338H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253122
Start	153693329:153693329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979C>G
AA Mutation	p.Leu327Val(p.L327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253122
Start	153694177:153694177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302G>A
Mutation Classification	Silent
Feature Type	Transcript