Primary Site >> Stomach Cancer

Gene >> RBL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373664
Start 37035455:37035455(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751292145
CDS Mutation c.1957G>A
AA Mutation p.Ala653Thr(p.A653T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373664
Start 36998830:36998830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3136G>A
AA Mutation p.Val1046Ile(p.V1046I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000373664
Start 37040179:37040179(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1877G>A
AA Mutation p.Arg626Gln(p.R626Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373664
Start 36998779:36998779(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3187A>C
AA Mutation p.Ser1063Arg(p.S1063R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000373664
Start 37044221:37044221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1635G>T
AA Mutation p.Glu545Asp(p.E545D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000373664
Start 37035497:37035497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1915T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000373664
Start 37044176:37044176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1680A>G
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000373664
Start 37061186:37061186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1167A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000373664
Start 37007534:37007534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2748T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000373664
Start 37032767:37032767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2280T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000373664
Start 37061105:37061105(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1248delT
AA Mutation p.Phe416LeufsTer13(p.F416Lfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000373664
Start 37068046:37068046(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.431delT
AA Mutation p.Leu144Ter(p.L144*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000373664
Start 37062177:37062178(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.931_989dupCTAACTGTTGGTGATTTTGATGAGAGGATCTTTTTGGGAGCAGACGCAGAAGAGGAAAT
AA Mutation p.Gly331Ter(p.G331*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000373664
Start 37003867:37003867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2872-1G>C
Mutation Classification Splice_Site
Feature Type Transcript