Primary Site >> Stomach Cancer

Gene >> FBXO31

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87343701:87343701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.554C>G
AA Mutation p.Pro185Arg(p.P185R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87334053:87334053(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1230G>T
AA Mutation p.Glu410Asp(p.E410D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000311635
Start 87347250:87347250(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413T>C
AA Mutation p.Leu138Pro(p.L138P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87335416:87335416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.884G>A
AA Mutation p.Arg295His(p.R295H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87336257:87336257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.740G>A
AA Mutation p.Arg247Gln(p.R247Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87360342:87360342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.365G>A
AA Mutation p.Arg122Gln(p.R122Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87360307:87360307(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778618544
CDS Mutation c.400G>A
AA Mutation p.Val134Ile(p.V134I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87334231:87334231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781136689
CDS Mutation c.1052G>A
AA Mutation p.Arg351Gln(p.R351Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000311635
Start 87335438:87335438(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.862C>A
AA Mutation p.Arg288Ser(p.R288S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87331342:87331342(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs544042571
CDS Mutation c.1566G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87343712:87343712(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762500727
CDS Mutation c.543C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87342910:87342910(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377117956
CDS Mutation c.699G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87331345:87331345(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550271598
CDS Mutation c.1563G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87335379:87335379(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.921T>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000311635
Start 87333960:87333960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1323G>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000311635
Start 87331453:87331453(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1455delC
AA Mutation p.Val487SerfsTer17(p.V487Sfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000311635
Start 87335334:87335334(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.966delC
AA Mutation p.His322GlnfsTer27(p.H322Qfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript