Colon Cancer: Gene >> NGF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369512
Start	115286611:115286611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369266810
CDS Mutation	c.185G>A
AA Mutation	p.Arg62His(p.R62H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369512
Start	115286651:115286651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146716262
CDS Mutation	c.145C>T
AA Mutation	p.Arg49Cys(p.R49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369512
Start	115286668:115286668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566033399
CDS Mutation	c.128C>T
AA Mutation	p.Ser43Phe(p.S43F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369512
Start	115286676:115286676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369512
Start	115286376:115286376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751386981
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369512
Start	115286460:115286460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.336delC
AA Mutation	p.Phe113SerfsTer45(p.F113Sfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NGF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369512
Start	115286228:115286228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>G
AA Mutation	p.Arg190Gly(p.R190G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369512
Start	115286637:115286637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376241395
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript