Colon Cancer: Gene >> UBE2Q1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154554745:154554745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578A>C
AA Mutation	p.Glu193Ala(p.E193A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154552450:154552450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Glu277Lys(p.E277K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154558246:154558246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154550947:154550947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754369992
CDS Mutation	c.1228G>A
AA Mutation	p.Glu410Lys(p.E410K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154553114:154553114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647A>C
AA Mutation	p.Lys216Thr(p.K216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292211
Start	154551436:154551436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292211
Start	154558287:154558287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292211
Start	154558276:154558276(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.278delC
AA Mutation	p.Pro93HisfsTer46(p.P93Hfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000292211
Start	154550939:154550940(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1235dupA
AA Mutation	p.Asn412LysfsTer31(p.N412Kfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UBE2Q1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292211
Start	154552122:154552122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>A
AA Mutation	p.Asp313Asn(p.D313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000292211
Start	154553036:154553036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725T>G
AA Mutation	p.Leu242Ter(p.L242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript