Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAGEA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286482
Start	149884694:149884694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Ser141Asn(p.S141N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286482
Start	149885163:149885163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286482
Start	149884431:149884431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286482
Start	149884392:149884392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286482
Start	149884497:149884497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286482
Start	149884633:149884633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782267175
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Cys(p.R121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286482
Start	149885173:149885173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Cys(p.R301C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286482
Start	149884713:149884713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript