Colon Cancer: Gene >> ATG101

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52073661:52073661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751591793
CDS Mutation	c.11G>A
AA Mutation	p.Arg4His(p.R4H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52073880:52073880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230G>A
AA Mutation	p.Arg77His(p.R77H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52073777:52073777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>T
AA Mutation	p.Gly43Cys(p.G43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52073846:52073846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Cys(p.R66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52077052:52077052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>T
AA Mutation	p.Glu173Asp(p.E173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52073778:52073778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128G>A
AA Mutation	p.Gly43Asp(p.G43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATG101

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336854
Start	52076858:52076858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553016999
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Cys(p.R109C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript