Mutation

Primary Site >> Liver Cancer

Gene >> FASN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82087379:82087379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141517558
CDS Mutation	c.3169A>G
AA Mutation	p.Ile1057Val(p.I1057V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82079406:82079406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776351410
CDS Mutation	c.7349C>T
AA Mutation	p.Thr2450Met(p.T2450M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82082031:82082031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6141A>C
AA Mutation	p.Lys2047Asn(p.K2047N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82080172:82080172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7114G>C
AA Mutation	p.Val2372Leu(p.V2372L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82085309:82085309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4216C>T
AA Mutation	p.Pro1406Ser(p.P1406S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82093308:82093308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566A>C
AA Mutation	p.Asn189Thr(p.N189T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82093615:82093615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437T>C
AA Mutation	p.Phe146Ser(p.F146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82087069:82087069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3408G>T
AA Mutation	p.Glu1136Asp(p.E1136D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82091516:82091516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771740708
CDS Mutation	c.1198G>A
AA Mutation	p.Val400Met(p.V400M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82085540:82085540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4064A>T
AA Mutation	p.Asp1355Val(p.D1355V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82083323:82083323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5444A>C
AA Mutation	p.Gln1815Pro(p.Q1815P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82093747:82093747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Gly102Glu(p.G102E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82092707:82092707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884C>T
AA Mutation	p.Thr295Ile(p.T295I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82082963:82082963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5718G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82087153:82087153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3324G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82080741:82080741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6777C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82084275:82084275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4878C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82081228:82081228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6531C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82083551:82083551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5307T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82083083:82083083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5598G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82080852:82080852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6666G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82081216:82081216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6543A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306749
Start	82092913:82092917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.758_762delCAGAT
AA Mutation	p.Thr253ArgfsTer31(p.T253Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306749
Start	82081250:82081250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6509delT
AA Mutation	p.Leu2170ProfsTer48(p.L2170Pfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000306749
Start	82089372:82089372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1978G>T
AA Mutation	p.Glu660Ter(p.E660*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript