Colon Cancer: Gene >> ULK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440863
Start	74843021:74843021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85T>A
AA Mutation	p.Tyr29Asn(p.Y29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000440863
Start	74840630:74840630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000440863
Start	74840314:74840314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000440863
Start	74841483:74841483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Trp(p.R131W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000440863
Start	74842337:74842337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186G>T
AA Mutation	p.Glu62Asp(p.E62D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ULK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000440863
Start	74840537:74840537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757280306
CDS Mutation	c.574G>A
AA Mutation	p.Ala192Thr(p.A192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript