Primary Site >> Stomach Cancer

Gene >> GNS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000258145
Start 64747838:64747838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.333C>A
AA Mutation p.Asn111Lys(p.N111K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000258145
Start 64737009:64737009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1093A>C
AA Mutation p.Ser365Arg(p.S365R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000258145
Start 64743142:64743142(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575544204
CDS Mutation c.791C>T
AA Mutation p.Thr264Met(p.T264M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000258145
Start 64720150:64720150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1452C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000258145
Start 64747733:64747733(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.438delT
AA Mutation p.Phe146LeufsTer6(p.F146Lfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000258145
Start 64747822:64747823(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.348dupG
AA Mutation p.Asn117GlufsTer4(p.N117Efs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript