Colon Cancer: Gene >> SETMAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358065
Start	4316602:4316602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Cys(p.R471C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358065
Start	4316624:4316624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433C>A
AA Mutation	p.Ser478Tyr(p.S478Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358065
Start	4316908:4316908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717C>G
AA Mutation	p.Leu573Val(p.L573V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358065
Start	4313221:4313221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374002434
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358065
Start	4317150:4317150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358065
Start	4316673:4316673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358065
Start	4303466:4303466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358065
Start	4313191:4313191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358065
Start	4313085:4313085(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.348delT
AA Mutation	p.Phe116LeufsTer58(p.F116Lfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000358065
Start	4317142:4317142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951G>T
AA Mutation	p.Glu651Ter(p.E651*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SETMAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358065
Start	4316534:4316534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1343A>T
AA Mutation	p.Lys448Met(p.K448M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000358065
Start	4313747:4313747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747095743
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Ter(p.R336*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript