Colon Cancer: Gene >> MAGEB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194621:26194621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762453651
CDS Mutation	c.775G>A
AA Mutation	p.Gly259Ser(p.G259S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194324:26194324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>T
AA Mutation	p.Gly160Cys(p.G160C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194805:26194805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959T>C
AA Mutation	p.Ile320Thr(p.I320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194603:26194603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757A>C
AA Mutation	p.Lys253Gln(p.K253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194544:26194544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698T>C
AA Mutation	p.Phe233Ser(p.F233S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379034
Start	26194443:26194443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370599063
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000379034
Start	26194606:26194606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760G>T
AA Mutation	p.Glu254Ter(p.E254*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAGEB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26195026:26195026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180G>A
AA Mutation	p.Ala394Thr(p.A394T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194448:26194448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768592764
CDS Mutation	c.602C>T
AA Mutation	p.Thr201Met(p.T201M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379034
Start	26194411:26194411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142927857
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Cys(p.R189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379034
Start	26194200:26194200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379034
Start	26194492:26194493(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.650dupT
AA Mutation	p.Leu217PhefsTer35(p.L217Ffs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript