Primary Site >> Stomach Cancer

Gene >> SMARCA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129465888:129465888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2773A>G
AA Mutation p.Arg925Gly(p.R925G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129487119:129487119(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140388140
CDS Mutation c.2116C>T
AA Mutation p.Arg706Cys(p.R706C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129516377:129516377(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.382C>T
AA Mutation p.Pro128Ser(p.P128S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129465572:129465572(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2978G>A
AA Mutation p.Arg993Gln(p.R993Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129465887:129465887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2774G>A
AA Mutation p.Arg925Lys(p.R925K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129465918:129465918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2743A>C
AA Mutation p.Ile915Leu(p.I915L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129480759:129480759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375431295
CDS Mutation c.2384G>A
AA Mutation p.Arg795His(p.R795H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129492069:129492069(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1687C>T
AA Mutation p.Pro563Ser(p.P563S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000371122
Start 129481146:129481146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2257C>T
AA Mutation p.Arg753Cys(p.R753C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000371122
Start 129504752:129504752(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1149C>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000371122
Start 129487107:129487107(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2128delA
AA Mutation p.Met710TrpfsTer6(p.M710Wfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000371122
Start 129471268:129471268(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2501delA
AA Mutation p.Lys834ArgfsTer50(p.K834Rfs*50)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000371122
Start 129488996:129488996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2038A>T
AA Mutation p.Lys680Ter(p.K680*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript