Primary Site >> Stomach Cancer

Gene >> RBM5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50093805:50093805(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.269A>C
AA Mutation p.Asp90Ala(p.D90A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000347869
Start 50115978:50115978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2092G>A
AA Mutation p.Glu698Lys(p.E698K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50092107:50092107(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.82C>T
AA Mutation p.Arg28Cys(p.R28C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50118434:50118434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2426C>A
AA Mutation p.Ala809Asp(p.A809D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50092162:50092162(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372517136
CDS Mutation c.137G>A
AA Mutation p.Arg46Gln(p.R46Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50092189:50092189(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746587173
CDS Mutation c.164G>A
AA Mutation p.Arg55Gln(p.R55Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000347869
Start 50110427:50110427(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1327G>A
AA Mutation p.Ala443Thr(p.A443T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000347869
Start 50107491:50107491(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.964delC
AA Mutation p.Leu322SerfsTer12(p.L322Sfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000347869
Start 50092188:50092188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.163C>T
AA Mutation p.Arg55Ter(p.R55*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript