Colon Cancer: Gene >> RTN4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000043402
Start	20242738:20242738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395T>C
AA Mutation	p.Leu132Pro(p.L132P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000043402
Start	20243018:20243018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115G>A
AA Mutation	p.Val39Met(p.V39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000043402
Start	20242385:20242385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747685263
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000043402
Start	20243026:20243026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107A>T
AA Mutation	p.Glu36Val(p.E36V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000043402
Start	20241921:20241921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000043402
Start	20241744:20241744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555150485
CDS Mutation	c.1389G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RTN4R

No Mutation Annotation!