Colon Cancer: Gene >> NOV

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259526
Start	119416588:119416588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56C>A
AA Mutation	p.Thr19Asn(p.T19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259526
Start	119416933:119416933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274A>T
AA Mutation	p.Ser92Cys(p.S92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259526
Start	119416936:119416936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259526
Start	119418228:119418228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>C
AA Mutation	p.Val161Leu(p.V161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259526
Start	119418161:119418161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOV

No Mutation Annotation!