Primary Site >> Stomach Cancer

Gene >> NFKBIB

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38907502:38907502(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764322441
CDS Mutation c.812T>C
AA Mutation p.Met271Thr(p.M271T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38907484:38907484(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567594250
CDS Mutation c.794C>T
AA Mutation p.Ala265Val(p.A265V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38908743:38908743(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759042553
CDS Mutation c.982G>A
AA Mutation p.Asp328Asn(p.D328N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38908815:38908815(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778168546
CDS Mutation c.1054G>A
AA Mutation p.Asp352Asn(p.D352N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38907451:38907451(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.761C>T
AA Mutation p.Ala254Val(p.A254V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38907642:38907642(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773488851
CDS Mutation c.952G>A
AA Mutation p.Asp318Asn(p.D318N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000313582
Start 38908768:38908768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1007G>A
AA Mutation p.Ser336Asn(p.S336N)
Mutation Classification Missense_Mutation
Feature Type Transcript