Primary Site >> Stomach Cancer

Gene >> IGF2BP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49041468:49041468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.909G>T
AA Mutation p.Glu303Asp(p.E303D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49046297:49046297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1565T>C
AA Mutation p.Val522Ala(p.V522A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49046361:49046361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1629C>A
AA Mutation p.Phe543Leu(p.F543L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49044051:49044051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1285A>G
AA Mutation p.Lys429Glu(p.K429E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 48999140:48999140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.207G>C
AA Mutation p.Glu69Asp(p.E69D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49038266:49038266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557111796
CDS Mutation c.500G>A
AA Mutation p.Arg167His(p.R167H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49038286:49038286(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779507141
CDS Mutation c.520C>T
AA Mutation p.Arg174Trp(p.R174W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000290341
Start 49045995:49045995(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781338712
CDS Mutation c.1501C>T
AA Mutation p.Arg501Trp(p.R501W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000290341
Start 49038354:49038354(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.592delC
AA Mutation p.Leu198PhefsTer32(p.L198Ffs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000290341
Start 49049423:49049423(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1714delG
AA Mutation p.Ala572ProfsTer53(p.A572Pfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000290341
Start 48997922:48997922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175+2T>C
Mutation Classification Splice_Site
Feature Type Transcript