Colon Cancer: Gene >> EGLN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250457
Start	33931193:33931193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380G>A
AA Mutation	p.Gly127Glu(p.G127E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250457
Start	33926999:33926999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>A
AA Mutation	p.Glu217Lys(p.E217K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250457
Start	33929083:33929083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375310922
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250457
Start	33950460:33950460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293T>C
AA Mutation	p.Ile98Thr(p.I98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250457
Start	33950672:33950672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EGLN3

No Mutation Annotation!