Primary Site >> Stomach Cancer

Gene >> VPS35

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46672363:46672363(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1270C>T
AA Mutation p.Leu424Phe(p.L424F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46671733:46671733(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780577406
CDS Mutation c.1496G>A
AA Mutation p.Arg499His(p.R499H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46662246:46662246(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2064G>T
AA Mutation p.Glu688Asp(p.E688D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46681488:46681488(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754806601
CDS Mutation c.212C>T
AA Mutation p.Ser71Phe(p.S71F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46680803:46680803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374C>A
AA Mutation p.Ser125Tyr(p.S125Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000299138
Start 46678987:46678987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676C>T
AA Mutation p.Arg226Cys(p.R226C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000299138
Start 46661823:46661823(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2106delA
AA Mutation p.Ala703LeufsTer2(p.A703Lfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000299138
Start 46681379:46681394(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.306_321delAAACATTATCCCAAGG
AA Mutation p.Asn103PhefsTer4(p.N103Ffs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript