Primary Site >> Stomach Cancer

Gene >> NUMA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72014199:72014199(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140741340
CDS Mutation c.3304G>A
AA Mutation p.Ala1102Thr(p.A1102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72013952:72013952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3551C>T
AA Mutation p.Ala1184Val(p.A1184V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72015248:72015248(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771552205
CDS Mutation c.2255G>A
AA Mutation p.Arg752Gln(p.R752Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72009079:72009079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762537230
CDS Mutation c.4946G>A
AA Mutation p.Arg1649Gln(p.R1649Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72015534:72015534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1969G>A
AA Mutation p.Ala657Thr(p.A657T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72013223:72013223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4280G>A
AA Mutation p.Arg1427Gln(p.R1427Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72016467:72016467(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1183T>C
AA Mutation p.Ser395Pro(p.S395P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72009004:72009004(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748328523
CDS Mutation c.5021G>A
AA Mutation p.Arg1674His(p.R1674H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72015665:72015665(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1838A>C
AA Mutation p.Lys613Thr(p.K613T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72013647:72013647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775941295
CDS Mutation c.3856C>T
AA Mutation p.Arg1286Cys(p.R1286C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72012428:72012428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4623G>T
AA Mutation p.Glu1541Asp(p.E1541D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72022354:72022354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357T>A
AA Mutation p.Phe119Leu(p.F119L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72004090:72004090(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113245212
CDS Mutation c.6133C>T
AA Mutation p.Arg2045Cys(p.R2045C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72008748:72008748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5156A>G
AA Mutation p.Asp1719Gly(p.D1719G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72009065:72009065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746224697
CDS Mutation c.4960C>T
AA Mutation p.Arg1654Trp(p.R1654W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72013193:72013193(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4310T>C
AA Mutation p.Leu1437Pro(p.L1437P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72003982:72003982(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149006752
CDS Mutation c.6241C>T
AA Mutation p.Arg2081Cys(p.R2081C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72013826:72013826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3677T>C
AA Mutation p.Leu1226Pro(p.L1226P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72018930:72018930(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.635C>T
AA Mutation p.Pro212Leu(p.P212L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72022398:72022398(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.313C>A
AA Mutation p.His105Asn(p.H105N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72014732:72014732(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750257826
CDS Mutation c.2771G>A
AA Mutation p.Arg924His(p.R924H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72018451:72018451(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805G>A
AA Mutation p.Ala269Thr(p.A269T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000393695
Start 72014733:72014733(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747075799
CDS Mutation c.2770C>T
AA Mutation p.Arg924Cys(p.R924C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72016000:72016000(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777949805
CDS Mutation c.1503C>T
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72004067:72004067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6156C>T
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72018270:72018270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.891G>A
Mutation Classification Silent
Feature Type Transcript
ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72029213:72029213(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.120T>C
Mutation Classification Silent
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72009283:72009283(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143949849
CDS Mutation c.4824G>A
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72015654:72015654(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1849C>T
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72021247:72021247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141785503
CDS Mutation c.417C>T
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72015631:72015631(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1872T>C
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000393695
Start 72014332:72014332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748155458
CDS Mutation c.3171G>A
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000393695
Start 72007357:72007357(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5295delC
AA Mutation p.Lys1766ArgfsTer2(p.K1766Rfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000393695
Start 72006044:72006044(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5683delG
AA Mutation p.Ala1895ProfsTer40(p.A1895Pfs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000393695
Start 72013144:72013144(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4359delG
AA Mutation p.Leu1454TrpfsTer54(p.L1454Wfs*54)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000393695
Start 72015445:72015445(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2058delA
AA Mutation p.Ala687GlnfsTer25(p.A687Qfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000393695
Start 72013017:72013017(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4486C>T
AA Mutation p.Arg1496Ter(p.R1496*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000393695
Start 72005266:72005267(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5795dupC
AA Mutation p.His1933ThrfsTer22(p.H1933Tfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 39
Mutation Consequence splice_donor_variant
Transcription ID ENST00000393695
Start 72018394:72018394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.860+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 40
Mutation Consequence inframe_deletion
Transcription ID ENST00000393695
Start 72017714:72017716(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1090_1092delAAG
AA Mutation p.Lys364del(p.K364del)
Mutation Classification In_Frame_Del
Feature Type Transcript