Primary Site >> Stomach Cancer

Gene >> RAB3IP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000550536
Start 69800221:69800221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.949T>G
AA Mutation p.Leu317Val(p.L317V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000550536
Start 69755532:69755532(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749687711
CDS Mutation c.172C>T
AA Mutation p.Arg58Trp(p.R58W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000550536
Start 69801655:69801655(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756676065
CDS Mutation c.1112T>C
AA Mutation p.Ile371Thr(p.I371T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000550536
Start 69756648:69756648(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745853351
CDS Mutation c.543C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000550536
Start 69801668:69801668(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1125A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000550536
Start 69812982:69812982(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1302delT
AA Mutation p.Phe434LeufsTer12(p.F434Lfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000550536
Start 69794500:69794501(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.718_719insTTAGCCTGAAGTT
AA Mutation p.Glu240ValfsTer11(p.E240Vfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript