Primary Site >> Stomach Cancer

Gene >> WDR11

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263461
Start 120865088:120865088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.755A>G
AA Mutation p.Tyr252Cys(p.Y252C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263461
Start 120885847:120885847(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1882A>G
AA Mutation p.Arg628Gly(p.R628G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263461
Start 120901074:120901074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2663A>G
AA Mutation p.Gln888Arg(p.Q888R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263461
Start 120865694:120865694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.944G>A
AA Mutation p.Arg315His(p.R315H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000263461
Start 120905993:120905993(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3414delT
AA Mutation p.Phe1138LeufsTer10(p.F1138Lfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000263461
Start 120871309:120871309(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs747938475
CDS Mutation c.1439delA
AA Mutation p.Asn480ThrfsTer32(p.N480Tfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000263461
Start 120866604:120866604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030C>T
AA Mutation p.Arg344Ter(p.R344*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000263461
Start 120851467:120851468(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.52dupG
AA Mutation p.Ala18GlyfsTer30(p.A18Gfs*30)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000263461
Start 120889999:120890000(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2333_2334insGAACCCT
AA Mutation p.Asp778GlufsTer5(p.D778Efs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000263461
Start 120862802:120862803(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.600dupA
AA Mutation p.Val201SerfsTer9(p.V201Sfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript