Mutation

Primary Site >> Stomach Cancer

Gene >> FASN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82086502:82086502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3484C>T
AA Mutation	p.Pro1162Ser(p.P1162S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82086499:82086499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201281021
CDS Mutation	c.3487G>A
AA Mutation	p.Gly1163Arg(p.G1163R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82091341:82091341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143812680
CDS Mutation	c.1373C>T
AA Mutation	p.Ala458Val(p.A458V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82088209:82088209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2692A>G
AA Mutation	p.Thr898Ala(p.T898A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82091441:82091441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781366271
CDS Mutation	c.1273C>T
AA Mutation	p.Arg425Trp(p.R425W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82081682:82081682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6325T>C
AA Mutation	p.Phe2109Leu(p.F2109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82083312:82083312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369955820
CDS Mutation	c.5455C>T
AA Mutation	p.Arg1819Trp(p.R1819W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82092519:82092519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965T>C
AA Mutation	p.Ile322Thr(p.I322T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82079513:82079513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7242G>T
AA Mutation	p.Gln2414His(p.Q2414H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82079157:82079157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7522G>A
AA Mutation	p.Val2508Met(p.V2508M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82087140:82087140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201182683
CDS Mutation	c.3337A>G
AA Mutation	p.Ile1113Val(p.I1113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82093630:82093630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>T
AA Mutation	p.Ala141Val(p.A141V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82093667:82093667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385G>T
AA Mutation	p.Gly129Cys(p.G129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82086487:82086487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758283388
CDS Mutation	c.3499G>T
AA Mutation	p.Ala1167Ser(p.A1167S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82081178:82081178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6581C>T
AA Mutation	p.Ala2194Val(p.A2194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82087813:82087813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202024339
CDS Mutation	c.2915C>T
AA Mutation	p.Pro972Leu(p.P972L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000306749
Start	82080198:82080198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7088C>T
AA Mutation	p.Ala2363Val(p.A2363V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82088445:82088445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370854247
CDS Mutation	c.2538C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82083611:82083611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776715958
CDS Mutation	c.5247G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82091331:82091331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565811170
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82089376:82089376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1974G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82080792:82080792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750578532
CDS Mutation	c.6726G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82088454:82088454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146170446
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82091050:82091050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747732644
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82082085:82082085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6087G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82087108:82087108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3369G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306749
Start	82079378:82079378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781074972
CDS Mutation	c.7377C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306749
Start	82085547:82085547(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4057delC
AA Mutation	p.Leu1353SerfsTer20(p.L1353Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306749
Start	82085288:82085289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4236dupC
AA Mutation	p.Ile1413HisfsTer22(p.I1413Hfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000306749
Start	82088877:82088877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript