Primary Site >> Stomach Cancer

Gene >> PRKDC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47777763:47777763(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11965C>T
AA Mutation p.Arg3989Trp(p.R3989W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47902768:47902768(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3070A>G
AA Mutation p.Thr1024Ala(p.T1024A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47831888:47831888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8191C>T
AA Mutation p.Arg2731Trp(p.R2731W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47889152:47889152(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4142G>A
AA Mutation p.Ser1381Asn(p.S1381N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47831923:47831923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8156C>T
AA Mutation p.Ala2719Val(p.A2719V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47828265:47828265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8480C>G
AA Mutation p.Ser2827Cys(p.S2827C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47934023:47934023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1565C>A
AA Mutation p.Pro522His(p.P522H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47863514:47863514(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5635G>A
AA Mutation p.Val1879Met(p.V1879M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47783764:47783764(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780805923
CDS Mutation c.11153G>A
AA Mutation p.Arg3718Gln(p.R3718Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47943277:47943277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.898T>C
AA Mutation p.Trp300Arg(p.W300R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47902746:47902746(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773506987
CDS Mutation c.3092G>A
AA Mutation p.Arg1031Gln(p.R1031Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47939583:47939583(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081A>G
AA Mutation p.Ile361Val(p.I361V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47854185:47854185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6791A>T
AA Mutation p.Asp2264Val(p.D2264V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47889129:47889129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4165G>A
AA Mutation p.Val1389Ile(p.V1389I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47936499:47936499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1132G>A
AA Mutation p.Ala378Thr(p.A378T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47834357:47834357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7991C>T
AA Mutation p.Thr2664Ile(p.T2664I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47857293:47857293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6472C>T
AA Mutation p.Arg2158Cys(p.R2158C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47882007:47882007(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4867C>A
AA Mutation p.Leu1623Met(p.L1623M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47902650:47902650(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3188T>G
AA Mutation p.Leu1063Arg(p.L1063R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47778557:47778557(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11755G>A
AA Mutation p.Gly3919Arg(p.G3919R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47936475:47936475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1156G>A
AA Mutation p.Val386Ile(p.V386I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47776955:47776955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12071G>A
AA Mutation p.Gly4024Glu(p.G4024E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47943357:47943357(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775322168
CDS Mutation c.818G>A
AA Mutation p.Arg273His(p.R273H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47788968:47788968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10840T>C
AA Mutation p.Tyr3614His(p.Y3614H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47834244:47834244(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs8178178
CDS Mutation c.8104A>G
AA Mutation p.Lys2702Glu(p.K2702E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47933082:47933082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1714G>A
AA Mutation p.Val572Ile(p.V572I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47939568:47939568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096T>C
AA Mutation p.Tyr366His(p.Y366H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47912415:47912415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2929G>A
AA Mutation p.Asp977Asn(p.D977N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47859634:47859634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6184G>A
AA Mutation p.Ala2062Thr(p.A2062T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47929879:47929879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2026A>G
AA Mutation p.Asn676Asp(p.N676D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47776926:47776926(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12100G>A
AA Mutation p.Ala4034Thr(p.A4034T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47849478:47849478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7031T>C
AA Mutation p.Leu2344Pro(p.L2344P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47859624:47859624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6194G>A
AA Mutation p.Arg2065His(p.R2065H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47902792:47902792(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3046G>A
AA Mutation p.Gly1016Arg(p.G1016R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47864651:47864651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5476A>G
AA Mutation p.Thr1826Ala(p.T1826A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47863573:47863573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5576A>G
AA Mutation p.Asn1859Ser(p.N1859S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47837361:47837361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375122519
CDS Mutation c.7612C>T
AA Mutation p.Arg2538Trp(p.R2538W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47939651:47939651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013T>C
AA Mutation p.Leu338Pro(p.L338P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47902786:47902786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376896763
CDS Mutation c.3052G>A
AA Mutation p.Val1018Met(p.V1018M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47789010:47789010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10798C>A
AA Mutation p.Pro3600Thr(p.P3600T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47820927:47820927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9128A>G
AA Mutation p.Tyr3043Cys(p.Y3043C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47794383:47794383(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10577C>T
AA Mutation p.Pro3526Leu(p.P3526L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47789191:47789191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10718A>G
AA Mutation p.Asn3573Ser(p.N3573S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000314191
Start 47859653:47859653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6165C>A
AA Mutation p.Ser2055Arg(p.S2055R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47935739:47935739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1440T>C
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47828189:47828189(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8556A>G
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47849288:47849288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7146G>A
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47831922:47831922(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750298710
CDS Mutation c.8157G>A
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47830671:47830671(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8331C>T
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47897279:47897279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3480C>T
Mutation Classification Silent
Feature Type Transcript
ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47821754:47821754(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8961A>G
Mutation Classification Silent
Feature Type Transcript
ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47897240:47897240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3519A>G
Mutation Classification Silent
Feature Type Transcript
ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47828294:47828294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8451G>A
Mutation Classification Silent
Feature Type Transcript
ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47799217:47799217(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10290T>C
Mutation Classification Silent
Feature Type Transcript
ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47785165:47785165(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11055C>A
Mutation Classification Silent
Feature Type Transcript
ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47834350:47834350(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769310297
CDS Mutation c.7998G>A
Mutation Classification Silent
Feature Type Transcript
ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47830614:47830614(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373077938
CDS Mutation c.8388C>T
Mutation Classification Silent
Feature Type Transcript
ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47862382:47862382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5910A>G
Mutation Classification Silent
Feature Type Transcript
ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47904971:47904971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2940A>G
Mutation Classification Silent
Feature Type Transcript
ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47859653:47859653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6165C>T
Mutation Classification Silent
Feature Type Transcript
ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000314191
Start 47912449:47912449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2895G>A
Mutation Classification Silent
Feature Type Transcript
ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47788994:47788994(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.10814delA
AA Mutation p.Asn3605ThrfsTer48(p.N3605Tfs*48)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47834238:47834238(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.8110delA
AA Mutation p.Arg2704GlyfsTer13(p.R2704Gfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47933058:47933058(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1738delG
AA Mutation p.Asp580IlefsTer23(p.D580Ifs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47830715:47830715(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.8287delA
AA Mutation p.Met2763Ter(p.M2763*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47782201:47782201(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.11450delT
AA Mutation p.Leu3817Ter(p.L3817*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000314191
Start 47836497:47836497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7792C>T
AA Mutation p.Arg2598Ter(p.R2598*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 68
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47828255:47828256(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.8489dupA
AA Mutation p.Asn2830LysfsTer16(p.N2830Kfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 69
Mutation Consequence frameshift_variant
Transcription ID ENST00000314191
Start 47776956:47776957(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.12069dupA
AA Mutation p.Gly4024ArgfsTer12(p.G4024Rfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 70
Mutation Consequence inframe_insertion
Transcription ID ENST00000314191
Start 47777811:47777812(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.11916_11917insAACAAAACCTACTTT
AA Mutation p.Leu3972_Pro3973insAsnLysThrTyrPhe(p.L3972_P3973insNKTYF)
Mutation Classification In_Frame_Ins
Feature Type Transcript