Mutation

Primary Site >> Stomach Cancer

Gene >> NOVA1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448776:26448776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707T>G
AA Mutation	p.Leu236Arg(p.L236R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448479:26448479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004G>T
AA Mutation	p.Gly335Val(p.G335V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26472363:26472363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476A>C
AA Mutation	p.Lys159Thr(p.K159T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448128:26448128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355G>T
AA Mutation	p.Gly452Val(p.G452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26479988:26479988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Cys(p.R146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448953:26448953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530T>C
AA Mutation	p.Ile177Thr(p.I177T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26480078:26480078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370779053
CDS Mutation	c.346A>G
AA Mutation	p.Ile116Val(p.I116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26447979:26447979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504A>G
AA Mutation	p.Asn502Asp(p.N502D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448759:26448759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724C>A
AA Mutation	p.Gln242Lys(p.Q242K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448578:26448578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905C>T
AA Mutation	p.Ala302Val(p.A302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26448161:26448161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>T
AA Mutation	p.Gly441Val(p.G441V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000539517
Start	26595415:26595415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275A>G
AA Mutation	p.Tyr92Cys(p.Y92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448451:26448451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448544:26448544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448189:26448189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1294T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448292:26448292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770857304
CDS Mutation	c.1191A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26480043:26480043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26447983:26447983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448787:26448787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539517
Start	26448919:26448919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539517
Start	26595432:26595435(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.255_258delGTCT
AA Mutation	p.Lys87ProfsTer14(p.K87Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539517
Start	26448102:26448103(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1380dupA
AA Mutation	p.Gly461ArgfsTer35(p.G461Rfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript