Colon Cancer: Gene >> USP22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21018004:21018004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21015785:21015785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805G>A
AA Mutation	p.Ala269Thr(p.A269T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21028644:21028644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770592022
CDS Mutation	c.202G>A
AA Mutation	p.Val68Ile(p.V68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21006962:21006962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256G>A
AA Mutation	p.Arg419Gln(p.R419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21019175:21019175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>T
AA Mutation	p.Glu143Asp(p.E143D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261497
Start	21021133:21021133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756302074
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261497
Start	21004960:21004960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261497
Start	21003066:21003066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> USP22

No Mutation Annotation!