Colon Cancer: Gene >> NBR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341165
Start	43197065:43197065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754168452
CDS Mutation	c.1985C>T
AA Mutation	p.Ala662Val(p.A662V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341165
Start	43189632:43189632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525G>T
AA Mutation	p.Gln175His(p.Q175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341165
Start	43193493:43193493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778919803
CDS Mutation	c.1379G>A
AA Mutation	p.Arg460His(p.R460H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341165
Start	43186357:43186357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315G>T
AA Mutation	p.Arg105Ser(p.R105S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341165
Start	43193169:43193169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341165
Start	43200372:43200372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs34660735
CDS Mutation	c.2236delC
AA Mutation	p.Leu746TrpfsTer50(p.L746Wfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000341165
Start	43191460:43191460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Glu318Ter(p.E318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341165
Start	43194383:43194384(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1560dupT
AA Mutation	p.Gly521TrpfsTer2(p.G521Wfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341165
Start	43200610:43200610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2468+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NBR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341165
Start	43193195:43193195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175T>G
AA Mutation	p.Phe392Cys(p.F392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341165
Start	43189605:43189605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341165
Start	43209945:43209945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2772C>A
Mutation Classification	Silent
Feature Type	Transcript