Colon Cancer: Gene >> PDCD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334409
Start	241851071:241851071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854C>A
AA Mutation	p.Ser285Tyr(p.S285Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334409
Start	241852744:241852744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313G>A
AA Mutation	p.Asp105Asn(p.D105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334409
Start	241851965:241851965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773349951
CDS Mutation	c.611G>A
AA Mutation	p.Arg204His(p.R204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334409
Start	241852662:241852662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756575544
CDS Mutation	c.395C>T
AA Mutation	p.Ala132Val(p.A132V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334409
Start	241852253:241852253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334409
Start	241851268:241851268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334409
Start	241852952:241852952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.105delC
AA Mutation	p.Thr36ProfsTer9(p.T36Pfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000334409
Start	241852621:241852621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>T
AA Mutation	p.Glu146Ter(p.E146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PDCD1

No Mutation Annotation!