Colon Cancer: Gene >> RTN4RL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335099
Start	57467795:57467795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537129988
CDS Mutation	c.218G>A
AA Mutation	p.Arg73His(p.R73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335099
Start	57467803:57467803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755532417
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Trp(p.R76W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335099
Start	57467614:57467614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140089941
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335099
Start	57476760:57476760(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1118delG
AA Mutation	p.Gly373AlafsTer151(p.G373Afs*151)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000335099
Start	57467977:57467977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400C>T
AA Mutation	p.Gln134Ter(p.Q134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RTN4RL2

No Mutation Annotation!