Colon Cancer: Gene >> UBE2K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39777740:39777740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39774903:39774903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369T>A
AA Mutation	p.Asp123Glu(p.D123E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39774854:39774854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199792616
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39755660:39755660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Trp(p.R74W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261427
Start	39777772:39777772(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.496delA
AA Mutation	p.Ile166Ter(p.I166*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UBE2K

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39755715:39755715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275G>A
AA Mutation	p.Cys92Tyr(p.C92Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261427
Start	39755688:39755688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248A>G
AA Mutation	p.Asn83Ser(p.N83S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript