Colon Cancer: Gene >> ATG7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11309006:11309006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Asp(p.G119D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11358497:11358497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364G>A
AA Mutation	p.Arg455His(p.R455H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11554832:11554832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101G>A
AA Mutation	p.Glu701Lys(p.E701K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11380038:11380038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1942G>T
AA Mutation	p.Ala648Ser(p.A648S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354449
Start	11313330:11313330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354449
Start	11347885:11347885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572456428
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354449
Start	11315490:11315490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354449
Start	11347984:11347984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354449
Start	11362830:11362830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1701C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATG7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11360615:11360615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514T>G
AA Mutation	p.Phe505Cys(p.F505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354449
Start	11333060:11333060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Glu286Lys(p.E286K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript