Primary Site >> Stomach Cancer

Gene >> BRCA2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32338533:32338533(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs398122776
CDS Mutation c.4178C>T
AA Mutation p.Ala1393Val(p.A1393V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32398636:32398636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10123A>G
AA Mutation p.Ser3375Gly(p.S3375G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32340158:32340158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5803A>G
AA Mutation p.Asn1935Asp(p.N1935D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000380152
Start 32356609:32356609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7617G>T
AA Mutation p.Gln2539His(p.Q2539H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32398298:32398298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9785A>C
AA Mutation p.Gln3262Pro(p.Q3262P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32398450:32398450(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9937A>C
AA Mutation p.Lys3313Gln(p.K3313Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32363403:32363403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8201C>A
AA Mutation p.Pro2734His(p.P2734H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32340960:32340960(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6605A>G
AA Mutation p.Asp2202Gly(p.D2202G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32332881:32332881(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1403G>T
AA Mutation p.Arg468Ile(p.R468I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32355208:32355208(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7355A>C
AA Mutation p.Asn2452Thr(p.N2452T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32332472:32332472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.994A>T
AA Mutation p.Ile332Phe(p.I332F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32354907:32354907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7054C>T
AA Mutation p.Pro2352Ser(p.P2352S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32398537:32398537(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs28897761
CDS Mutation c.10024G>A
AA Mutation p.Glu3342Lys(p.E3342K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32398766:32398766(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778034661
CDS Mutation c.10253T>G
AA Mutation p.Ile3418Ser(p.I3418S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32336911:32336911(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2556C>G
AA Mutation p.Asn852Lys(p.N852K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32332959:32332959(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs786202205
CDS Mutation c.1481T>C
AA Mutation p.Val494Ala(p.V494A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32332521:32332521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1043T>C
AA Mutation p.Val348Ala(p.V348A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32337716:32337716(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3361T>A
AA Mutation p.Ser1121Thr(p.S1121T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32337830:32337830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3475T>A
AA Mutation p.Cys1159Ser(p.C1159S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32380030:32380030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9141G>C
AA Mutation p.Gln3047His(p.Q3047H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32339210:32339210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4855A>G
AA Mutation p.Asn1619Asp(p.N1619D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32354904:32354904(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs80358930
CDS Mutation c.7051G>A
AA Mutation p.Ala2351Thr(p.A2351T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32338368:32338368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4013G>A
AA Mutation p.Gly1338Asp(p.G1338D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32340420:32340420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6065C>T
AA Mutation p.Ser2022Leu(p.S2022L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32337699:32337699(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3344C>T
AA Mutation p.Ser1115Phe(p.S1115F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32357757:32357757(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs80358990
CDS Mutation c.7633G>A
AA Mutation p.Val2545Ile(p.V2545I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32338670:32338670(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs80358666
CDS Mutation c.4315G>A
AA Mutation p.Ala1439Thr(p.A1439T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000380152
Start 32379414:32379414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8852C>T
AA Mutation p.Ala2951Val(p.A2951V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32338093:32338093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3738T>C
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32341102:32341102(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs786201405
CDS Mutation c.6747C>T
Mutation Classification Silent
Feature Type Transcript
ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32340848:32340848(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767202483
CDS Mutation c.6493T>C
Mutation Classification Silent
Feature Type Transcript
ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32340385:32340385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6030C>A
Mutation Classification Silent
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32339725:32339725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5370A>G
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32339815:32339815(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758869410
CDS Mutation c.5460C>T
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32337178:32337178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2823G>C
Mutation Classification Silent
Feature Type Transcript
ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32332858:32332858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1380T>C
Mutation Classification Silent
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32340100:32340100(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs1799953
CDS Mutation c.5745G>A
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32338930:32338930(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762189076
CDS Mutation c.4575T>C
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000380152
Start 32370491:32370491(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371278843
CDS Mutation c.8421G>A
Mutation Classification Silent
Feature Type Transcript
ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32338201:32338202(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs746229647
CDS Mutation c.3847_3848delGT
AA Mutation p.Val1283LysfsTer2(p.V1283Kfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32339933:32339933(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5583delA
AA Mutation p.Val1862Ter(p.V1862*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32336624:32336625(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2271_2272delAA
AA Mutation p.Leu759PhefsTer3(p.L759Ffs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32337615:32337615(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3263delC
AA Mutation p.Pro1088LeufsTer16(p.P1088Lfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32338382:32338382(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4031delA
AA Mutation p.Asn1344MetfsTer30(p.N1344Mfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32333284:32333284(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs80359307
CDS Mutation c.1813delA
AA Mutation p.Ile605TyrfsTer9(p.I605Yfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32339422:32339422(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5073delA
AA Mutation p.Lys1691AsnfsTer15(p.K1691Nfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32379886:32379886(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs762120301
CDS Mutation c.9097delA
AA Mutation p.Thr3033LeufsTer29(p.T3033Lfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32398756:32398756(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.10248delA
AA Mutation p.Lys3416AsnfsTer11(p.K3416Nfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32337185:32337185(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2835delA
AA Mutation p.Asp946IlefsTer14(p.D946Ifs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32356531:32356531(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7543delA
AA Mutation p.Thr2515HisfsTer9(p.T2515Hfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32337306:32337306(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2957delA
AA Mutation p.Asn986IlefsTer5(p.N986Ifs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000380152
Start 32363286:32363286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8084C>A
AA Mutation p.Ser2695Ter(p.S2695*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32340725:32340726(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.6370_6371insCTTGCTTTCC
AA Mutation p.Lys2124ThrfsTer8(p.K2124Tfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 54
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32339699:32339700(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5351dupA
AA Mutation p.Asn1784LysfsTer3(p.N1784Kfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 55
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32340747:32340748(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.6392_6393insC
AA Mutation p.Lys2131AsnfsTer5(p.K2131Nfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32379495:32379496(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.8940dupA
AA Mutation p.Glu2981ArgfsTer37(p.E2981Rfs*37)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32380135:32380136(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.9253dupA
AA Mutation p.Thr3085AsnfsTer26(p.T3085Nfs*26)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000380152
Start 32337184:32337185(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2835dupA
AA Mutation p.Asp946ArgfsTer13(p.D946Rfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript