C2675520[trait identifier] AND "Department of Medical and Surgical Sci - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 51329	NM_000059.4(BRCA2):c.26C>T (p.Pro9Leu)	BRCA2 (P9L)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 2683817	NM_000059.4(BRCA2):c.41T>C (p.Ile14Thr)	BRCA2 (I14T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 91755	NM_000059.4(BRCA2):c.172G>A (p.Glu58Lys)	BRCA2 (E58K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 37803	NM_000059.4(BRCA2):c.280C>T (p.Pro94Ser)	BRCA2 (P94S)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 409529	NM_000059.4(BRCA2):c.335G>A (p.Ser112Asn)	BRCA2 (S112N)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GUncertain significance
Select item 1169708	NM_000059.4(BRCA2):c.476-3dup	BRCA2	Duplication (intron variant)	Hereditary breast ovarian cancer syndrome	GBenign
Select item 37924	NM_000059.4(BRCA2):c.476-3C>A	BRCA2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 495466	NM_000059.4(BRCA2):c.476T>C (p.Val159Ala)	BRCA2 (V159A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 51818	NM_000059.4(BRCA2):c.520C>T (p.Arg174Cys)	BRCA2 (R174C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 51921	NM_000059.4(BRCA2):c.572A>T (p.Asp191Val)	BRCA2 (D191V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 140966	NM_000059.4(BRCA2):c.599C>T (p.Thr200Ile)	BRCA2 (T200I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 186155	NM_000059.4(BRCA2):c.620C>T (p.Thr207Ile)	BRCA2 (T207I)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 52920	NM_000059.4(BRCA2):c.992A>T (p.Lys331Ile)	BRCA2 (K331I)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 51068	NM_000059.4(BRCA2):c.1127T>G (p.Phe376Cys)	BRCA2 (F376C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 96761	NM_000059.4(BRCA2):c.1146A>T (p.Lys382Asn)	BRCA2 (K382N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +10 more	GConflicting classifications of pathogenicity
Select item 51090	NM_000059.4(BRCA2):c.1244A>G (p.His415Arg)	BRCA2 (H415R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 51105	NM_000059.4(BRCA2):c.1342C>T (p.Arg448Cys)	BRCA2 (R448C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 220031	NM_000059.4(BRCA2):c.1462A>C (p.Ile488Leu)	BRCA2 (I488L)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 37745	NM_000059.4(BRCA2):c.1550A>G (p.Asn517Ser)	BRCA2 (N517S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 142782	NM_000059.4(BRCA2):c.1714G>A (p.Val572Ile)	BRCA2 (V572I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 51189	NM_000059.4(BRCA2):c.1769T>G (p.Phe590Cys)	BRCA2 (F590C)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 51192	NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	BRCA2 (D596H)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 37760	NM_000059.4(BRCA2):c.1810A>G (p.Lys604Glu)	BRCA2 (K604E)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51207	NM_000059.4(BRCA2):c.1820A>C (p.Lys607Thr)	BRCA2 (K607T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 820475	NM_000059.4(BRCA2):c.1991G>A (p.Gly664Glu)	BRCA2 (G664E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 219593	NM_000059.4(BRCA2):c.1996A>G (p.Ile666Val)	BRCA2 (I666V)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 91768	NM_000059.4(BRCA2):c.2045T>C (p.Ile682Thr)	BRCA2 (I682T)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +2 more	GConflicting classifications of pathogenicity
Select item 462257	NM_000059.4(BRCA2):c.2104A>G (p.Ile702Val)	BRCA2 (I702V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 820929	NM_000059.4(BRCA2):c.2273G>A (p.Ser758Asn)	BRCA2 (S758N)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2 +2 more	GConflicting classifications of pathogenicity
Select item 37781	NM_000059.4(BRCA2):c.2320A>G (p.Thr774Ala)	BRCA2 (T774A)	Single nucleotide variant (missense variant)	BRCA2-related condition +5 more	GConflicting classifications of pathogenicity
Select item 821334	NM_000059.4(BRCA2):c.2475T>C (p.Asn825=)	BRCA2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 231761	NM_000059.4(BRCA2):c.2492T>C (p.Val831Ala)	BRCA2 (V831A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 96782	NM_000059.4(BRCA2):c.2755G>A (p.Glu919Lys)	BRCA2 (E919K)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 51372	NM_000059.4(BRCA2):c.2926_2927delinsAT (p.Ser976Ile)	BRCA2 (S976I)	Indel (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 51375	NM_000059.4(BRCA2):c.2944A>C (p.Ile982Leu)	BRCA2 (I982L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 420747	NM_000059.4(BRCA2):c.3071T>A (p.Ile1024Asn)	BRCA2 (I1024N)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2 +3 more	GConflicting classifications of pathogenicity
Select item 37844	NM_000059.4(BRCA2):c.3509C>T (p.Ala1170Val)	BRCA2 (A1170V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 2683818	NM_000059.4(BRCA2):c.3519T>G (p.Ile1173Met)	BRCA2 (I1173M)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 51515	NM_000059.4(BRCA2):c.3749A>G (p.Glu1250Gly)	BRCA2 (E1250G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 627710	NM_000059.4(BRCA2):c.3854A>G (p.Glu1285Gly)	BRCA2 (E1285G)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 185122	NM_000059.4(BRCA2):c.3865A>G (p.Lys1289Glu)	BRCA2 (K1289E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 37868	NM_000059.4(BRCA2):c.3966_3968del (p.Asn1322del)	BRCA2	Deletion (inframe_deletion)	BRCA2-related condition +5 more	GUncertain significance
Select item 37874	NM_000059.4(BRCA2):c.4054G>T (p.Asp1352Tyr)	BRCA2 (D1352Y)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 2683819	NM_000059.4(BRCA2):c.4291G>A (p.Ala1431Thr)	BRCA2 (A1431T)	Single nucleotide variant (intron variant +2 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 156168	NM_000059.4(BRCA2):c.4391C>T (p.Ser1464Phe)	BRCA2 (S1464F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1366992	NM_000059.4(BRCA2):c.4603G>T (p.Ala1535Ser)	BRCA2 (A1535S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 2683820	NM_000059.4(BRCA2):c.4826C>G (p.Thr1609Ser)	BRCA2 (T1609S)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 185896	NM_000059.4(BRCA2):c.5200G>A (p.Glu1734Lys)	BRCA2 (E1734K)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 419201	NM_000059.4(BRCA2):c.5386G>T (p.Asp1796Tyr)	BRCA2 (D1796Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 51852	NM_000059.4(BRCA2):c.5390C>G (p.Ala1797Gly)	BRCA2 (A1797G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 51860	NM_000059.4(BRCA2):c.5428G>A (p.Val1810Ile)	BRCA2 (V1810I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 141212	NM_000059.4(BRCA2):c.5465A>T (p.Asn1822Ile)	BRCA2 (N1822I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 141782	NM_000059.4(BRCA2):c.5492T>C (p.Ile1831Thr)	BRCA2 (I1831T)	Single nucleotide variant (missense variant)	BRCA2-related condition +5 more	GConflicting classifications of pathogenicity
Select item 142634	NM_000059.4(BRCA2):c.5498A>G (p.Asn1833Ser)	BRCA2 (N1833S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 2683821	NM_000059.4(BRCA2):c.5543G>C (p.Ser1848Thr)	BRCA2 (S1848T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 51895	NM_000059.4(BRCA2):c.5635G>A (p.Glu1879Lys)	BRCA2 (E1879K)	Single nucleotide variant (missense variant)	BRCA2-related condition +6 more	GConflicting classifications of pathogenicity
Select item 142686	NM_000059.4(BRCA2):c.5671G>A (p.Ala1891Thr)	BRCA2 (A1891T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 186838	NM_000059.4(BRCA2):c.5677T>G (p.Cys1893Gly)	BRCA2 (C1893G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 187246	NM_000059.4(BRCA2):c.5702A>T (p.Glu1901Val)	BRCA2 (E1901V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 2683822	NM_000059.4(BRCA2):c.5705A>C (p.Asp1902Ala)	BRCA2 (D1902A)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 2683823	NM_000059.4(BRCA2):c.5731G>C (p.Asp1911His)	BRCA2 (D1911H)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 142228	NM_000059.4(BRCA2):c.5870T>C (p.Ile1957Thr)	BRCA2 (I1957T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 409413	NM_000059.4(BRCA2):c.5885T>C (p.Ile1962Thr)	BRCA2 (I1962T)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 185748	NM_000059.4(BRCA2):c.6062A>G (p.His2021Arg)	BRCA2 (H2021R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 38032	NM_000059.4(BRCA2):c.6290C>T (p.Thr2097Met)	BRCA2 (T2097M)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 141259	NM_000059.4(BRCA2):c.6479A>G (p.Gln2160Arg)	BRCA2 (Q2160R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 577437	NM_000059.4(BRCA2):c.6505A>T (p.Thr2169Ser)	BRCA2 (T2169S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 52123	NM_000059.4(BRCA2):c.6532C>A (p.His2178Asn)	BRCA2 (H2178N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 431193	NM_000059.4(BRCA2):c.6562A>G (p.Lys2188Glu)	BRCA2 (K2188E)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1349558	NM_000059.4(BRCA2):c.6652G>A (p.Asp2218Asn)	BRCA2 (D2218N)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 52151	NM_000059.4(BRCA2):c.6665A>G (p.Tyr2222Cys)	BRCA2 (Y2222C)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 52199	NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	BRCA2 (G2274V)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +8 more	GConflicting classifications of pathogenicity
Select item 52239	NM_000059.4(BRCA2):c.7007+5G>A	BRCA2	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 52260	NM_000059.4(BRCA2):c.7057G>C (p.Gly2353Arg)	BRCA2 (G2353R)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 462440	NM_000059.4(BRCA2):c.7462A>G (p.Arg2488Gly)	BRCA2 (R2488G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 481550	NM_000059.4(BRCA2):c.7524C>T (p.Gly2508=)	BRCA2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 52349	NM_000059.4(BRCA2):c.7534C>T (p.Leu2512Phe)	BRCA2 (L2512F)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GBenign
Select item 96855	NM_000059.4(BRCA2):c.7628A>G (p.Tyr2543Cys)	BRCA2 (Y2543C)	Single nucleotide variant (missense variant)	not specified +13 more	GUncertain significance
Select item 141335	NM_000059.4(BRCA2):c.7759C>T (p.Leu2587Phe)	BRCA2 (L2587F)	Single nucleotide variant (missense variant)	BRCA2-related condition +5 more	GConflicting classifications of pathogenicity
Select item 2026523	NM_000059.4(BRCA2):c.7769C>T (p.Ser2590Phe)	BRCA2 (S946F +3 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 91492	NM_000059.4(BRCA2):c.7786G>A (p.Gly2596Arg)	BRCA2 (G2596R)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 38138	NM_000059.4(BRCA2):c.8092G>A (p.Ala2698Thr)	BRCA2 (A2698T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 409489	NM_000059.4(BRCA2):c.8222A>G (p.Lys2741Arg)	BRCA2 (K2741R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 156176	NM_000059.4(BRCA2):c.8262T>G (p.His2754Gln)	BRCA2 (H2754Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 52546	NM_000059.4(BRCA2):c.8324T>C (p.Met2775Thr)	BRCA2 (M2775T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 52559	NM_000059.4(BRCA2):c.8351G>A (p.Arg2784Gln)	BRCA2 (R2784Q)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 38158	NM_000059.4(BRCA2):c.8378G>T (p.Gly2793Val)	BRCA2 (G2793V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 91511	NM_000059.4(BRCA2):c.8386C>T (p.Pro2796Ser)	BRCA2 (P2796S)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +3 more	GConflicting classifications of pathogenicity
Select item 96868	NM_000059.4(BRCA2):c.8471G>C (p.Arg2824Thr)	BRCA2 (R2824T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 462492	NM_000059.4(BRCA2):c.8704G>A (p.Ala2902Thr)	BRCA2 (A2902T)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +2 more	GUncertain significance
Select item 584863	NM_000059.4(BRCA2):c.8754+9G>A	BRCA2	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 2 +1 more	GConflicting classifications of pathogenicity
Select item 52692	NM_000059.4(BRCA2):c.8850G>T (p.Lys2950Asn)	BRCA2 (K2950N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 38200	NM_000059.4(BRCA2):c.8972G>A (p.Arg2991His)	BRCA2 (R2991H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 52725	NM_000059.4(BRCA2):c.9006A>T (p.Glu3002Asp)	BRCA2 (E3002D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 52742	NM_000059.4(BRCA2):c.9076C>G (p.Gln3026Glu)	BRCA2 (Q3026E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 38211	NM_000059.4(BRCA2):c.9104A>C (p.Tyr3035Ser)	BRCA2 (Y3035S)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 52760	NM_000059.4(BRCA2):c.9118G>A (p.Val3040Ile)	BRCA2 (V3040I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1062244	NM_000059.4(BRCA2):c.9218A>C (p.Asp3073Ala)	BRCA2 (D3073A)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 126203	NM_000059.4(BRCA2):c.9227G>T (p.Gly3076Val)	BRCA2 (G3076V)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic FDA Recognized database
Select item 38233	NM_000059.4(BRCA2):c.9371A>T (p.Asn3124Ile)	BRCA2 (N3124I)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic

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