Primary Site >> Stomach Cancer

Gene >> ARID5B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62000144:62000144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556C>T
AA Mutation p.Arg186Trp(p.R186W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62091522:62091522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2059A>G
AA Mutation p.Met687Val(p.M687V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62092489:62092489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3026C>G
AA Mutation p.Ala1009Gly(p.A1009G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62092650:62092650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376805718
CDS Mutation c.3187G>A
AA Mutation p.Gly1063Arg(p.G1063R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62057274:62057274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1004G>A
AA Mutation p.Arg335Lys(p.R335K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62091021:62091021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1558A>G
AA Mutation p.Thr520Ala(p.T520A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62092305:62092305(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2842C>G
AA Mutation p.Arg948Gly(p.R948G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62092333:62092333(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2870T>C
AA Mutation p.Val957Ala(p.V957A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 62091726:62091726(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750226503
CDS Mutation c.2263G>A
AA Mutation p.Val755Ile(p.V755I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000279873
Start 61940282:61940282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.376G>A
AA Mutation p.Ala126Thr(p.A126T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000279873
Start 62000155:62000155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.567G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000279873
Start 62092130:62092130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2667G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000279873
Start 62091344:62091344(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755912811
CDS Mutation c.1881C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000279873
Start 62050979:62050979(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.825C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000279873
Start 62090946:62090946(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1489delA
AA Mutation p.Ile497Ter(p.I497*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000279873
Start 62092359:62092359(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2901delA
AA Mutation p.Lys967AsnfsTer15(p.K967Nfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000279873
Start 62092358:62092359(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2901dupA
AA Mutation p.Tyr968IlefsTer3(p.Y968Ifs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript