Colon Cancer: Gene >> ACSL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109678343:109678343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851G>T
AA Mutation	p.Arg284Leu(p.R284L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109659453:109659453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879G>A
AA Mutation	p.Ala627Thr(p.A627T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109661574:109661574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777A>G
AA Mutation	p.Lys593Glu(p.K593E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109663342:109663342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574A>C
AA Mutation	p.Asn525Thr(p.N525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109644048:109644048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2117G>A
AA Mutation	p.Arg706Gln(p.R706Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340800
Start	109683468:109683468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19G>C
AA Mutation	p.Val7Leu(p.V7L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000340800
Start	109644030:109644030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2135A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340800
Start	109644158:109644158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2007C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340800
Start	109683292:109683292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200252463
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340800
Start	109678006:109678006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340800
Start	109683367:109683367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000340800
Start	109683397:109683397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>A
AA Mutation	p.Trp30Ter(p.W30*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000340800
Start	109659372:109659372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960C>T
AA Mutation	p.Arg654Ter(p.R654*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340800
Start	109683470:109683471(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.16_17insGAGT
AA Mutation	p.Asn6ArgfsTer45(p.N6Rfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACSL4

No Mutation Annotation!