Colon Cancer: Gene >> ACSL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112413302:112413302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078G>T
AA Mutation	p.Asp360Tyr(p.D360Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112408497:112408497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112410608:112410608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186230656
CDS Mutation	c.769G>A
AA Mutation	p.Val257Ile(p.V257I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112426827:112426827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1879G>A
AA Mutation	p.Gly627Arg(p.G627R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112422373:112422373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525G>A
AA Mutation	p.Glu509Lys(p.E509K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112404571:112404571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326A>G
AA Mutation	p.Lys109Arg(p.K109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354273
Start	112410627:112410627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788G>T
AA Mutation	p.Gly263Val(p.G263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000354273
Start	112422440:112422440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375823791
CDS Mutation	c.1592C>T
AA Mutation	p.Pro531Leu(p.P531L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354273
Start	112422411:112422411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000354273
Start	112425389:112425389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1645C>T
AA Mutation	p.Gln549Ter(p.Q549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000354273
Start	112410583:112410583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACSL5

No Mutation Annotation!