Colon Cancer: Gene >> UCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310473
Start	73977931:73977931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780835346
CDS Mutation	c.292G>A
AA Mutation	p.Gly98Ser(p.G98S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310473
Start	73978069:73978069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781271646
CDS Mutation	c.154C>T
AA Mutation	p.Arg52Cys(p.R52C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310473
Start	73977959:73977959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765681329
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310473
Start	73978347:73978347(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.32delC
AA Mutation	p.Pro11LeufsTer5(p.P11Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000310473
Start	73977885:73977885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773260052
CDS Mutation	c.337+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> UCP2

No Mutation Annotation!