Colon Cancer: Gene >> RNF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367510
Start	185098194:185098194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587G>A
AA Mutation	p.Arg196Gln(p.R196Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367510
Start	185093151:185093151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>G
AA Mutation	p.Ile113Met(p.I113M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367510
Start	185093178:185093178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367510
Start	185100214:185100214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.928delT
AA Mutation	p.Ser310LeufsTer12(p.S310Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367510
Start	185100261:185100262(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.971_972insA
AA Mutation	p.Met325HisfsTer16(p.M325Hfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367510
Start	185087630:185087630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000367510
Start	185099870:185099870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Ter(p.R273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript