Colon Cancer: Gene >> MAGEA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151924355:151924355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150785634
CDS Mutation	c.691G>C
AA Mutation	p.Val231Leu(p.V231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151924163:151924163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778001194
CDS Mutation	c.499G>A
AA Mutation	p.Val167Met(p.V167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151924209:151924209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Cys182Tyr(p.C182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151924455:151924455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Asp(p.G264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151924110:151924110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Pro149Leu(p.P149L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276344
Start	151924285:151924285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276344
Start	151923961:151923961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761277562
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276344
Start	151923804:151923804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140T>C
AA Mutation	p.Val47Ala(p.V47A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276344
Start	151924306:151924306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376198310
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript