Primary Site >> Stomach Cancer

Gene >> NEU1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375631
Start 31860182:31860182(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779431356
CDS Mutation c.881G>A
AA Mutation p.Arg294His(p.R294H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375631
Start 31861286:31861286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.517T>C
AA Mutation p.Trp173Arg(p.W173R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000375631
Start 31862111:31862111(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.240G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375631
Start 31862078:31862078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.273C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000375631
Start 31861341:31861342(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.461dupT
AA Mutation p.Tyr155LeufsTer23(p.Y155Lfs*23)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript