Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAGEA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152767116:152767116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>T
AA Mutation	p.Ala179Ser(p.A179S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152766758:152766758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893G>A
AA Mutation	p.Arg298His(p.R298H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152767411:152767411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240G>T
AA Mutation	p.Trp80Cys(p.W80C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152767412:152767412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239G>T
AA Mutation	p.Trp80Leu(p.W80L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152766962:152766962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689T>G
AA Mutation	p.Val230Gly(p.V230G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329342
Start	152766837:152766837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329342
Start	152767060:152767060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329342
Start	152767497:152767497(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.154delG
AA Mutation	p.Glu52ArgfsTer24(p.E52Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329342
Start	152767145:152767145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>G
AA Mutation	p.Val169Gly(p.V169G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329342
Start	152767362:152767362(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.289delA
AA Mutation	p.Thr97ProfsTer53(p.T97Pfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000329342
Start	152767279:152767279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372T>G
AA Mutation	p.Tyr124Ter(p.Y124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000329342
Start	152767278:152767278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Ter(p.R125*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript