Colon Cancer: Gene >> NEGR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357731
Start	71776259:71776259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375935233
CDS Mutation	c.448G>A
AA Mutation	p.Val150Ile(p.V150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357731
Start	71592832:71592832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925A>C
AA Mutation	p.Ser309Arg(p.S309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357731
Start	71935268:71935268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220C>T
AA Mutation	p.Arg74Trp(p.R74W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357731
Start	71698060:71698060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357731
Start	72282450:72282450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357731
Start	71407494:71407494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357731
Start	71611061:71611061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369017807
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357731
Start	71592816:71592816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NEGR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357731
Start	71935170:71935170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript