Colon Cancer: Gene >> RNF146

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368314
Start	127286929:127286929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316T>C
AA Mutation	p.Trp106Arg(p.W106R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368314
Start	127286726:127286726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>T
AA Mutation	p.Ala38Val(p.A38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368314
Start	127287421:127287421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808C>A
AA Mutation	p.His270Asn(p.H270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368314
Start	127287587:127287587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748615447
CDS Mutation	c.974G>A
AA Mutation	p.Arg325Gln(p.R325Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368314
Start	127287378:127287378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>A
AA Mutation	p.Asp255Glu(p.D255E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368314
Start	127287324:127287324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368314
Start	127287210:127287210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140369665
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000368314
Start	127287115:127287115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Ter(p.R168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNF146

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000368314
Start	127287595:127287595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Ter(p.R328*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript