Colon Cancer: Gene >> NEUROG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314744
Start	135535282:135535282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747790479
CDS Mutation	c.409G>A
AA Mutation	p.Ala137Thr(p.A137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314744
Start	135535360:135535360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331G>A
AA Mutation	p.Ala111Thr(p.A111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314744
Start	135535283:135535283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000314744
Start	135535189:135535189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748863808
CDS Mutation	c.502C>T
AA Mutation	p.Gln168Ter(p.Q168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NEUROG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314744
Start	135535408:135535408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283G>A
AA Mutation	p.Val95Ile(p.V95I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript