Colon Cancer: Gene >> ATG13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46667862:46667862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127C>G
AA Mutation	p.Ala376Gly(p.A376G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46665501:46665501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46657568:46657568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641A>G
AA Mutation	p.His214Arg(p.H214R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46672325:46672325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547T>C
AA Mutation	p.Leu516Pro(p.L516P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46657109:46657109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759630324
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359513
Start	46645380:46645380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359513
Start	46664953:46664953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359513
Start	46668510:46668510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778394445
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATG13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46657110:46657110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359513
Start	46672287:46672287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1509G>T
AA Mutation	p.Glu503Asp(p.E503D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript