Mutation

Primary Site >> Stomach Cancer

Gene >> NLRP3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247423313:247423313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367T>C
AA Mutation	p.Tyr123His(p.Y123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424174:247424174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731C>T
AA Mutation	p.Ala244Val(p.A244V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424438:247424438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995T>C
AA Mutation	p.Leu332Pro(p.L332P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247444085:247444085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2783G>A
AA Mutation	p.Gly928Glu(p.G928E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247425148:247425148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104895389
CDS Mutation	c.1705G>A
AA Mutation	p.Glu569Lys(p.E569K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247418838:247418838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44A>G
AA Mutation	p.Glu15Gly(p.E15G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424123:247424123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180177493
CDS Mutation	c.680C>T
AA Mutation	p.Ala227Val(p.A227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247423874:247423874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>C
AA Mutation	p.Val144Ala(p.V144A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424773:247424773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201252712
CDS Mutation	c.1330G>A
AA Mutation	p.Val444Ile(p.V444I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424498:247424498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055C>A
AA Mutation	p.Pro352His(p.P352H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247444748:247444748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2938G>C
AA Mutation	p.Asp980His(p.D980H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247418972:247418972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Asp60Asn(p.D60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424812:247424812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1369A>G
AA Mutation	p.Ser457Gly(p.S457G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247425005:247425005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562T>A
AA Mutation	p.Ile521Asn(p.I521N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247424483:247424483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040T>G
AA Mutation	p.Leu347Arg(p.L347R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247425317:247425317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874C>A
AA Mutation	p.Pro625His(p.P625H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000336119
Start	247425299:247425299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856A>C
AA Mutation	p.Lys619Thr(p.K619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247418905:247418905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247435988:247435988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2517C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247424073:247424073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247419070:247419070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771343047
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247418836:247418836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247425066:247425066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774490246
CDS Mutation	c.1623A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247425279:247425279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247425189:247425189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247424766:247424766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201976178
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336119
Start	247418962:247418962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336119
Start	247424804:247424804(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1364delG
AA Mutation	p.Gly455GlufsTer49(p.G455Efs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336119
Start	247424676:247424676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1237delC
AA Mutation	p.Leu413TrpfsTer10(p.L413Wfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000336119
Start	247436142:247436142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript