Colon Cancer: Gene >> UNC93B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227471
Start	67998382:67998382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747214914
CDS Mutation	c.758C>T
AA Mutation	p.Thr253Met(p.T253M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227471
Start	67999659:67999659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414G>T
AA Mutation	p.Met138Ile(p.M138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000227471
Start	67999627:67999627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446T>C
AA Mutation	p.Phe149Ser(p.F149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000227471
Start	68003119:68003119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295T>C
AA Mutation	p.Tyr99His(p.Y99H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227471
Start	67996740:67996740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227471
Start	67995755:67995755(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1219delG
AA Mutation	p.Ala407ProfsTer42(p.A407Pfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UNC93B1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000227471
Start	67993787:67993787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1371G>A
Mutation Classification	Silent
Feature Type	Transcript