Primary Site >> Stomach Cancer

Gene >> SYT8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000381968
Start 1837264:1837264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1039C>A
AA Mutation p.Leu347Met(p.L347M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000381968
Start 1837397:1837397(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754418253
CDS Mutation c.1172G>A
AA Mutation p.Arg391His(p.R391H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000381968
Start 1837318:1837318(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1093C>A
AA Mutation p.His365Asn(p.H365N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000381968
Start 1837343:1837343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1118G>T
AA Mutation p.Arg373Leu(p.R373L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000381968
Start 1835921:1835921(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.340delG
AA Mutation p.Asp114MetfsTer25(p.D114Mfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000381968
Start 1835938:1835938(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.357delG
AA Mutation p.Cys120AlafsTer19(p.C120Afs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000381968
Start 1836165:1836165(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.443delG
AA Mutation p.Gly148AlafsTer115(p.G148Afs*115)
Mutation Classification Frame_Shift_Del
Feature Type Transcript