Colon Cancer: Gene >> UBE2L3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342192
Start	21592930:21592930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97T>A
AA Mutation	p.Leu33Met(p.L33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342192
Start	21610933:21610933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200A>C
AA Mutation	p.Lys67Thr(p.K67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342192
Start	21610876:21610876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143A>C
AA Mutation	p.Lys48Thr(p.K48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342192
Start	21610937:21610937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000342192
Start	21592938:21592938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105G>A
AA Mutation	p.Trp35Ter(p.W35*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000342192
Start	21610885:21610890(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.154_159delAGAATC
AA Mutation	p.Arg52_Ile53del(p.R52_I53del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UBE2L3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342192
Start	21611010:21611010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>A
AA Mutation	p.Glu93Lys(p.E93K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342192
Start	21610931:21610931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757743777
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript