Colon Cancer: Gene >> NPTXR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333039
Start	38826571:38826571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027C>T
AA Mutation	p.Pro343Ser(p.P343S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333039
Start	38822800:38822800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312G>T
AA Mutation	p.Ala438Ser(p.A438S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333039
Start	38828356:38828356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200507552
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333039
Start	38822693:38822693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NPTXR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333039
Start	38828310:38828310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827G>C
AA Mutation	p.Gly276Ala(p.G276A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333039
Start	38826673:38826673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368736692
CDS Mutation	c.925G>A
AA Mutation	p.Val309Met(p.V309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript