Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ATG10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282185
Start	82178531:82178531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>A
AA Mutation	p.His133Asn(p.H133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282185
Start	82164447:82164447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>C
AA Mutation	p.Ala89Pro(p.A89P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282185
Start	82252609:82252609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282185
Start	82252586:82252586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.483delT
AA Mutation	p.Phe161LeufsTer12(p.F161Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000282185
Start	82178539:82178539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405C>A
AA Mutation	p.Cys135Ter(p.C135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000282185
Start	82164397:82164397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.217-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ATG10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282185
Start	81987642:81987642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72A>T
AA Mutation	p.Gln24His(p.Q24H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000282185
Start	81987622:81987622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>T
AA Mutation	p.Glu18Ter(p.E18*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000282185
Start	82058604:82058604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript