Colon Cancer: Gene >> NRN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244766
Start	6002395:6002395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158C>T
AA Mutation	p.Pro53Leu(p.P53L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244766
Start	5999080:5999080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244766
Start	5999145:5999145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260C>T
AA Mutation	p.Ala87Val(p.A87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244766
Start	6002437:6002437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116C>T
AA Mutation	p.Ser39Leu(p.S39L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000244766
Start	5999146:5999146(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.259delG
AA Mutation	p.Ala87ArgfsTer8(p.A87Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NRN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244766
Start	5999080:5999080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244766
Start	5999081:5999081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751041560
CDS Mutation	c.324C>T
Mutation Classification	Silent
Feature Type	Transcript