Colon Cancer: Gene >> UBA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361055
Start	69056052:69056052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196C>T
AA Mutation	p.Ser399Phe(p.S399F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361055
Start	69077841:69077841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140G>A
AA Mutation	p.Arg47Gln(p.R47Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361055
Start	69055904:69055904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Ser417Leu(p.S417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361055
Start	69064070:69064070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373601125
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361055
Start	69056692:69056692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003G>A
AA Mutation	p.Ala335Thr(p.A335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361055
Start	69056811:69056811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361055
Start	69056675:69056675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361055
Start	69056617:69056617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361055
Start	69063069:69063069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.606delG
AA Mutation	p.Thr203GlnfsTer10(p.T203Qfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UBA3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361055
Start	69064070:69064070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373601125
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript