Primary Site >> Stomach Cancer

Gene >> NEDD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266742
Start 96952034:96952034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1964G>T
AA Mutation p.Arg655Ile(p.R655I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266742
Start 96912740:96912740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.154G>A
AA Mutation p.Ala52Thr(p.A52T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266742
Start 96951458:96951458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1838A>T
AA Mutation p.Asn613Ile(p.N613I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000266742
Start 96935146:96935146(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.660G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000266742
Start 96943639:96943639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1374T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000266742
Start 96943656:96943656(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1395delT
AA Mutation p.Phe465LeufsTer15(p.F465Lfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000266742
Start 96940437:96940438(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1147_1148delTT
AA Mutation p.Leu383IlefsTer2(p.L383Ifs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript