Colon Cancer: Gene >> MAGEA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153183155:153183155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Asp256Asn(p.D256N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153182721:153182721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>A
AA Mutation	p.Gly111Asp(p.G111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153182651:153182651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262C>G
AA Mutation	p.Pro88Ala(p.P88A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153183243:153183243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854A>G
AA Mutation	p.Lys285Arg(p.K285R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153182770:153182770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381A>C
AA Mutation	p.Glu127Asp(p.E127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153183010:153183010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153183256:153183256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153182563:153182563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153182893:153182893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153183260:153183260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Cys(p.R291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153183170:153183170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356661
Start	153182962:153182962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>T
AA Mutation	p.Lys191Asn(p.K191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153182488:153182488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356661
Start	153182887:153182887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript