Colon Cancer: Gene >> ACSL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184770425:184770425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>A
AA Mutation	p.Ala323Thr(p.A323T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184763175:184763175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200424498
CDS Mutation	c.1513G>A
AA Mutation	p.Glu505Lys(p.E505K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184757178:184757178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534896186
CDS Mutation	c.2044C>T
AA Mutation	p.Arg682Trp(p.R682W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184760467:184760467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672C>T
AA Mutation	p.His558Tyr(p.H558Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184788692:184788692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235G>A
AA Mutation	p.Asp79Asn(p.D79N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184770439:184770439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>A
AA Mutation	p.Ser318Tyr(p.S318Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184763240:184763240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448C>T
AA Mutation	p.Pro483Leu(p.P483L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184803471:184803471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44T>C
AA Mutation	p.Leu15Pro(p.L15P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184757868:184757868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1835C>T
AA Mutation	p.Ala612Val(p.A612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281455
Start	184803481:184803481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34A>G
AA Mutation	p.Met12Val(p.M12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281455
Start	184783984:184783984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281455
Start	184768337:184768337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281455
Start	184776655:184776655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281455
Start	184765923:184765923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000281455
Start	184776965:184776965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>T
AA Mutation	p.Gly166Ter(p.G166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281455
Start	184776649:184776650(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.589_590dupCT
AA Mutation	p.Val198TrpfsTer14(p.V198Wfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ACSL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281455
Start	184803416:184803416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368853187
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript