Mutation

Primary Site >> Stomach Cancer

Gene >> NEO1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73289188:73289188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3692G>T
AA Mutation	p.Arg1231Leu(p.R1231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73298534:73298534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4088C>T
AA Mutation	p.Ala1363Val(p.A1363V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73236481:73236481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426T>C
AA Mutation	p.Phe476Leu(p.F476L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73298546:73298546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4100T>C
AA Mutation	p.Ile1367Thr(p.I1367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73254752:73254752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757256214
CDS Mutation	c.2015G>A
AA Mutation	p.Arg672His(p.R672H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73282978:73282978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776944418
CDS Mutation	c.3277C>T
AA Mutation	p.His1093Tyr(p.H1093Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73260442:73260442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2375G>A
AA Mutation	p.Arg792His(p.R792H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73178364:73178364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228T>C
AA Mutation	p.Cys410Arg(p.C410R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73260318:73260318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140293397
CDS Mutation	c.2251G>A
AA Mutation	p.Val751Ile(p.V751I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73178396:73178396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260A>T
AA Mutation	p.Gln420His(p.Q420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73135905:73135905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893T>C
AA Mutation	p.Val298Ala(p.V298A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261908
Start	73249701:73249701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874C>T
AA Mutation	p.Ala625Val(p.A625V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73293403:73293403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3756C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73236435:73236435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73302631:73302631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4321C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261908
Start	73288439:73288439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3537A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261908
Start	73298378:73298378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3933delC
AA Mutation	p.Met1312CysfsTer48(p.M1312Cfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73116687:73116687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278T>A
AA Mutation	p.Leu93Ter(p.L93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73270420:73270420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2823G>A
AA Mutation	p.Trp941Ter(p.W941*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73249706:73249706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879C>T
AA Mutation	p.Arg627Ter(p.R627*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73116551:73116551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
AA Mutation	p.Arg48Ter(p.R48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000261908
Start	73270195:73270195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2680C>T
AA Mutation	p.Arg894Ter(p.R894*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261908
Start	73249624:73249625(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1803dupA
AA Mutation	p.Tyr602IlefsTer5(p.Y602Ifs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	24
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261908
Start	73278129:73278129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3194-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript