Primary Site >> Stomach Cancer

Gene >> VPS13A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77209518:77209518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481C>T
AA Mutation p.Arg161Cys(p.R161C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77370556:77370556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8885G>A
AA Mutation p.Arg2962His(p.R2962H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360280
Start 77238189:77238189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1783G>A
AA Mutation p.Ala595Thr(p.A595T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77295837:77295837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781120866
CDS Mutation c.3803G>A
AA Mutation p.Arg1268Gln(p.R1268Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77339838:77339838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6701G>A
AA Mutation p.Arg2234Gln(p.R2234Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77238064:77238064(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200416908
CDS Mutation c.1658G>A
AA Mutation p.Arg553His(p.R553H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77282265:77282265(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3109A>G
AA Mutation p.Lys1037Glu(p.K1037E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77260124:77260124(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779216309
CDS Mutation c.2327G>A
AA Mutation p.Arg776Gln(p.R776Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77337412:77337412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6253A>C
AA Mutation p.Lys2085Gln(p.K2085Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77209519:77209519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482G>A
AA Mutation p.Arg161His(p.R161H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77275579:77275579(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774586650
CDS Mutation c.2594G>A
AA Mutation p.Arg865Gln(p.R865Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77339849:77339849(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779178649
CDS Mutation c.6712C>T
AA Mutation p.Pro2238Ser(p.P2238S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77332037:77332037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6019T>C
AA Mutation p.Ser2007Pro(p.S2007P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77337500:77337500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367713644
CDS Mutation c.6341G>A
AA Mutation p.Arg2114Gln(p.R2114Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77221300:77221300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105T>C
AA Mutation p.Tyr369His(p.Y369H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77370483:77370483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8812G>C
AA Mutation p.Asp2938His(p.D2938H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77370484:77370484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8813A>T
AA Mutation p.Asp2938Val(p.D2938V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77177763:77177763(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.59T>C
AA Mutation p.Val20Ala(p.V20A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77321729:77321729(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772519124
CDS Mutation c.5813T>C
AA Mutation p.Leu1938Pro(p.L1938P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77339603:77339603(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6466A>C
AA Mutation p.Lys2156Gln(p.K2156Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77250148:77250148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2089A>C
AA Mutation p.Asn697His(p.N697H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77366765:77366765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8364A>C
AA Mutation p.Glu2788Asp(p.E2788D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77337321:77337321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6162G>C
AA Mutation p.Glu2054Asp(p.E2054D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77238380:77238380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1894G>A
AA Mutation p.Ala632Thr(p.A632T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77337471:77337471(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6312A>G
AA Mutation p.Ile2104Met(p.I2104M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77318436:77318436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5158G>A
AA Mutation p.Glu1720Lys(p.E1720K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000360280
Start 77227417:77227417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1384G>A
AA Mutation p.Glu462Lys(p.E462K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77353450:77353450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7461T>C
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77228142:77228142(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1473T>C
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77293487:77293487(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762176805
CDS Mutation c.3486G>A
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77275635:77275635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2650A>C
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77205326:77205326(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.201T>G
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77339827:77339827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139115188
CDS Mutation c.6690C>T
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000360280
Start 77345134:77345134(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7281C>T
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77221303:77221303(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs779822889
CDS Mutation c.1115delA
AA Mutation p.Lys372SerfsTer2(p.K372Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77369392:77369392(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.8653delT
AA Mutation p.Tyr2885MetfsTer20(p.Y2885Mfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77225933:77225933(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1174delA
AA Mutation p.Thr392ProfsTer7(p.T392Pfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77337327:77337327(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6173delA
AA Mutation p.Asn2058MetfsTer6(p.N2058Mfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77337313:77337313(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6156delT
AA Mutation p.Phe2052LeufsTer5(p.F2052Lfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77321183:77321183(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5434delA
AA Mutation p.Met1812TrpfsTer30(p.M1812Wfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77316253:77316253(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4715delA
AA Mutation p.Asn1572MetfsTer6(p.N1572Mfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 42
Mutation Consequence stop_gained
Transcription ID ENST00000360280
Start 77318310:77318310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5032G>T
AA Mutation p.Glu1678Ter(p.E1678*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000360280
Start 77318362:77318362(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5084T>A
AA Mutation p.Leu1695Ter(p.L1695*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000360280
Start 77295836:77295836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3802C>T
AA Mutation p.Arg1268Ter(p.R1268*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77260134:77260135(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2343dupA
AA Mutation p.Leu782ThrfsTer9(p.L782Tfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77275511:77275512(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2532dupT
AA Mutation p.Asp845Ter(p.D845*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000360280
Start 77315280:77315281(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4446dupA
AA Mutation p.Asp1483ArgfsTer17(p.D1483Rfs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 48
Mutation Consequence splice_donor_variant
Transcription ID ENST00000360280
Start 77221358:77221358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1161+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 49
Mutation Consequence splice_donor_variant
Transcription ID ENST00000360280
Start 77226600:77226600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1357+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 50
Mutation Consequence splice_donor_variant
Transcription ID ENST00000360280
Start 77340283:77340283(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.6879+1delG
Mutation Classification Splice_Site
Feature Type Transcript