ClinVar Miner

List of variants in gene BRCA2 reported as pathogenic for gastric cancer

Included ClinVar conditions (22):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.9382C>T (p.Arg3128Ter) rs80359212 0.00004
NM_000059.4(BRCA2):c.5645C>A (p.Ser1882Ter) rs80358785 0.00002
NM_000059.4(BRCA2):c.10150C>T (p.Arg3384Ter) rs397507568 0.00001
NM_000059.4(BRCA2):c.7480C>T (p.Arg2494Ter) rs80358972 0.00001
NM_000059.4(BRCA2):c.8243G>A (p.Gly2748Asp) rs80359071 0.00001
NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=) rs28897756 0.00001
NM_000059.3(BRCA2):c.2808_2811del (p.Ala938Profs) rs80359351
NM_000059.4(BRCA2):c.10061del (p.Ser3354fs) rs2073055112
NM_000059.4(BRCA2):c.10062del (p.Gly3355fs)
NM_000059.4(BRCA2):c.10220_10223del (p.Asn3407fs) rs2137667778
NM_000059.4(BRCA2):c.1156del (p.Glu386fs) rs397507262
NM_000059.4(BRCA2):c.1184G>A (p.Trp395Ter) rs886040347
NM_000059.4(BRCA2):c.1261C>T (p.Gln421Ter) rs80358419
NM_000059.4(BRCA2):c.1278del (p.Asp427fs) rs80359274
NM_000059.4(BRCA2):c.1389_1390del (p.Val464fs) rs80359283
NM_000059.4(BRCA2):c.1399A>T (p.Lys467Ter) rs80358427
NM_000059.4(BRCA2):c.1411G>T (p.Glu471Ter) rs80358428
NM_000059.4(BRCA2):c.145G>T (p.Glu49Ter) rs80358435
NM_000059.4(BRCA2):c.1770del (p.Phe590fs)
NM_000059.4(BRCA2):c.1813del (p.Ile605fs) rs80359306
NM_000059.4(BRCA2):c.1909+1G>A rs587781629
NM_000059.4(BRCA2):c.2368del (p.Glu790fs)
NM_000059.4(BRCA2):c.2516_2519del (p.Lys838_Tyr839insTer)
NM_000059.4(BRCA2):c.2581C>T (p.Gln861Ter) rs773356478
NM_000059.4(BRCA2):c.2802del (p.Asp935fs)
NM_000059.4(BRCA2):c.2950del (p.Glu984fs)
NM_000059.4(BRCA2):c.316+2T>C rs81002805
NM_000059.4(BRCA2):c.3235del (p.Ser1079fs) rs397507660
NM_000059.4(BRCA2):c.3296C>G (p.Ser1099Ter) rs397507663
NM_000059.4(BRCA2):c.3481_3482del (p.Asp1161fs)
NM_000059.4(BRCA2):c.3572del (p.Lys1191fs)
NM_000059.4(BRCA2):c.3599_3600del (p.Asp1199_Cys1200insTer) rs80359391
NM_000059.4(BRCA2):c.3847_3848del (p.Val1283fs) rs80359405
NM_000059.4(BRCA2):c.3940A>T (p.Lys1314Ter)
NM_000059.4(BRCA2):c.4284dup (p.Gln1429fs) rs80359439
NM_000059.4(BRCA2):c.4339del (p.Ile1446_Val1447insTer) rs80359443
NM_000059.4(BRCA2):c.4415_4418del (p.Lys1472fs) rs397507333
NM_000059.4(BRCA2):c.4478_4481del (p.Glu1493fs) rs80359454
NM_000059.4(BRCA2):c.4539_4542del (p.Asp1513fs)
NM_000059.4(BRCA2):c.4649_4650del (p.Glu1550fs) rs1593903006
NM_000059.4(BRCA2):c.475+1G>A rs81002797
NM_000059.4(BRCA2):c.4808dup (p.Asn1603fs) rs80359466
NM_000059.4(BRCA2):c.4822G>T (p.Glu1608Ter) rs1566231194
NM_000059.4(BRCA2):c.4867C>T (p.Gln1623Ter)
NM_000059.4(BRCA2):c.4888del (p.Ser1630fs)
NM_000059.4(BRCA2):c.4903_4904del (p.Leu1635fs) rs80359471
NM_000059.4(BRCA2):c.4948del (p.Ser1650fs) rs80359474
NM_000059.4(BRCA2):c.4952del (p.Pro1651fs) rs397507752
NM_000059.4(BRCA2):c.5073dup (p.Trp1692fs) rs80359479
NM_000059.4(BRCA2):c.5130_5133del (p.Asp1709_Tyr1710insTer) rs80359484
NM_000059.4(BRCA2):c.5279C>A (p.Ser1760Ter) rs80358751
NM_000059.4(BRCA2):c.5482_5486del (p.Lys1828fs) rs80359516
NM_000059.4(BRCA2):c.5576_5579del (p.Ile1859fs) rs80359520
NM_000059.4(BRCA2):c.5598dup (p.Thr1867fs)
NM_000059.4(BRCA2):c.5635G>T (p.Glu1879Ter) rs55996097
NM_000059.4(BRCA2):c.5722_5723del (p.Leu1908fs) rs80359530
NM_000059.4(BRCA2):c.5773_5774del (p.Gln1925fs) rs2072538071
NM_000059.4(BRCA2):c.5851_5854del (p.Ser1951fs) rs80359543
NM_000059.4(BRCA2):c.5980C>T (p.Gln1994Ter) rs80358831
NM_000059.4(BRCA2):c.6063_6066del (p.His2021fs)
NM_000059.4(BRCA2):c.6348del (p.Cys2117fs)
NM_000059.4(BRCA2):c.6359C>A (p.Ser2120Ter)
NM_000059.4(BRCA2):c.6405_6409del (p.Asn2135fs) rs80359584
NM_000059.4(BRCA2):c.6445dup (p.Ile2149fs)
NM_000059.4(BRCA2):c.6461_6473del (p.Tyr2154fs)
NM_000059.4(BRCA2):c.6468_6469del (p.Gln2157fs) rs80359596
NM_000059.4(BRCA2):c.6553del (p.Ala2185fs) rs80359603
NM_000059.4(BRCA2):c.658_659del (p.Val220fs) rs80359604
NM_000059.4(BRCA2):c.6620_6623del (p.Thr2207fs)
NM_000059.4(BRCA2):c.6649A>T (p.Lys2217Ter) rs1555284779
NM_000059.4(BRCA2):c.6656C>A (p.Ser2219Ter)
NM_000059.4(BRCA2):c.682-1G>T rs81002831
NM_000059.4(BRCA2):c.6922A>T (p.Lys2308Ter)
NM_000059.4(BRCA2):c.6952C>T (p.Arg2318Ter) rs80358920
NM_000059.4(BRCA2):c.755_758del (p.Asp252fs) rs80359659
NM_000059.4(BRCA2):c.7819_7820del (p.Thr2607fs) rs2137576469
NM_000059.4(BRCA2):c.793+2T>G rs886040942
NM_000059.4(BRCA2):c.798del (p.Phe266fs) rs886040739
NM_000059.4(BRCA2):c.8005A>T (p.Arg2669Ter)
NM_000059.4(BRCA2):c.8023A>G (p.Ile2675Val) rs397507954
NM_000059.4(BRCA2):c.805dup (p.Thr269fs) rs886040744
NM_000059.4(BRCA2):c.8140C>T (p.Gln2714Ter) rs80359058
NM_000059.4(BRCA2):c.8168A>G (p.Asp2723Gly) rs41293513
NM_000059.4(BRCA2):c.8364G>A (p.Trp2788Ter) rs397507981
NM_000059.4(BRCA2):c.8488-1G>A rs397507404
NM_000059.4(BRCA2):c.8629G>T (p.Glu2877Ter) rs80359121
NM_000059.4(BRCA2):c.9076C>T (p.Gln3026Ter) rs80359159
NM_000059.4(BRCA2):c.9097dup (p.Thr3033fs) rs397507419
NM_000059.4(BRCA2):c.9212dup (p.Val3072fs) rs1555288557
NM_000059.4(BRCA2):c.9648+1G>T

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