Colon Cancer: Gene >> USP39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323701
Start	85636083:85636083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980T>C
AA Mutation	p.Leu327Pro(p.L327P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323701
Start	85636116:85636116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013A>C
AA Mutation	p.Lys338Thr(p.K338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323701
Start	85641054:85641054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363A>C
AA Mutation	p.Lys455Gln(p.K455Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323701
Start	85647945:85647945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579T>C
AA Mutation	p.Tyr527His(p.Y527H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323701
Start	85630783:85630783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323701
Start	85619269:85619269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753735784
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323701
Start	85644951:85644951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> USP39

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323701
Start	85645063:85645063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143344250
CDS Mutation	c.1543C>T
AA Mutation	p.Arg515Trp(p.R515W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript