Primary Site >> Stomach Cancer

Gene >> NLRC4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32238284:32238284(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202095832
CDS Mutation c.2369T>C
AA Mutation p.Leu790Pro(p.L790P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32235536:32235536(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780229500
CDS Mutation c.2647G>A
AA Mutation p.Ala883Thr(p.A883T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32250498:32250498(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1366A>G
AA Mutation p.Ser456Gly(p.S456G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32224598:32224598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2950G>A
AA Mutation p.Val984Ile(p.V984I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32250545:32250545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1319A>C
AA Mutation p.Lys440Thr(p.K440T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32250746:32250746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1118A>C
AA Mutation p.Lys373Thr(p.K373T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32250021:32250021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1843G>T
AA Mutation p.Asp615Tyr(p.D615Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32251419:32251419(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs572809664
CDS Mutation c.445G>A
AA Mutation p.Val149Met(p.V149M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32251376:32251376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.488G>T
AA Mutation p.Ser163Ile(p.S163I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32250500:32250500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1364T>C
AA Mutation p.Leu455Pro(p.L455P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32251589:32251589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.275A>T
AA Mutation p.Gln92Leu(p.Q92L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32241059:32241059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2324T>C
AA Mutation p.Met775Thr(p.M775T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360906
Start 32251190:32251190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.674G>A
AA Mutation p.Gly225Asp(p.G225D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000360906
Start 32251140:32251140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.724A>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000360906
Start 32224494:32224494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3054T>G
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000360906
Start 32251144:32251144(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.720G>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000360906
Start 32252620:32252621(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.60_61insCTTGCAGA
AA Mutation p.Lys21LeufsTer16(p.K21Lfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript