Colon Cancer: Gene >> ACSL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222909136:222909136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364A>C
AA Mutation	p.Lys122Gln(p.K122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222923084:222923084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087A>C
AA Mutation	p.Lys363Gln(p.K363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222909089:222909089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Gly106Glu(p.G106E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222908933:222908933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Arg54Gln(p.R54Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222934655:222934655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973T>C
AA Mutation	p.Val658Ala(p.V658A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222941533:222941533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042G>A
AA Mutation	p.Arg681His(p.R681H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222924519:222924519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145813997
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Cys(p.R406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357430
Start	222934560:222934560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781721691
CDS Mutation	c.1878G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACSL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222930777:222930777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697G>T
AA Mutation	p.Gly566Val(p.G566V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357430
Start	222918147:222918147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658A>C
AA Mutation	p.Lys220Gln(p.K220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357430
Start	222919102:222919102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>A
Mutation Classification	Silent
Feature Type	Transcript