Colon Cancer: Gene >> CENPA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335756
Start	26792133:26792133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141275453
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335756
Start	26792233:26792233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203G>A
AA Mutation	p.Ser68Asn(p.S68N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335756
Start	26792157:26792157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000335756
Start	26792803:26792803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258G>A
AA Mutation	p.Trp86Ter(p.W86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000335756
Start	26792762:26792762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217G>T
AA Mutation	p.Glu73Ter(p.E73*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CENPA

No Mutation Annotation!