Primary Site >> Stomach Cancer

Gene >> BUB1B

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000287598
Start 40217497:40217497(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2680A>G
AA Mutation p.Ile894Val(p.I894V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000287598
Start 40202591:40202591(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1631C>A
AA Mutation p.Pro544His(p.P544H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40176480:40176480(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587778144
CDS Mutation c.388C>T
AA Mutation p.Arg130Cys(p.R130C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40170635:40170635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.338A>C
AA Mutation p.Lys113Thr(p.K113T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40202609:40202609(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs28989187
CDS Mutation c.1649G>A
AA Mutation p.Arg550Gln(p.R550Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40220602:40220602(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377612791
CDS Mutation c.2996G>A
AA Mutation p.Arg999Gln(p.R999Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40206372:40206372(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1923A>C
AA Mutation p.Glu641Asp(p.E641D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40209667:40209667(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2176T>C
AA Mutation p.Tyr726His(p.Y726H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000287598
Start 40170574:40170574(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277G>A
AA Mutation p.Gly93Arg(p.G93R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000287598
Start 40217616:40217616(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755014372
CDS Mutation c.2799A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000287598
Start 40220567:40220567(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2964delA
AA Mutation p.Asp989MetfsTer13(p.D989Mfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000287598
Start 40185305:40185305(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.897delC
AA Mutation p.Met300CysfsTer31(p.M300Cfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000287598
Start 40212550:40212550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2437G>T
AA Mutation p.Glu813Ter(p.E813*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript