"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2774822	NM_007294.4(BRCA1):c.*104G>A	BRCA1	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 928073	NM_007294.4(BRCA1):c.101_103del	BRCA1	Deletion (3 prime UTR variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GUncertain significance
Select item 141903	NM_007294.4(BRCA1):c.*1C>T	BRCA1	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 185343	NM_007294.4(BRCA1):c.5586C>T (p.His1862=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 55637	NM_007294.4(BRCA1):c.5585A>T (p.His1862Leu)	BRCA1 (H1862L +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GBenign/Likely benign
Select item 1381587	NM_007294.4(BRCA1):c.5582G>A (p.Ser1861Asn)	BRCA1 (S1814N +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +1 more	GUncertain significance
Select item 186496	NM_007294.4(BRCA1):c.5573T>C (p.Ile1858Thr)	BRCA1 (I1858T +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 183951	NM_007294.4(BRCA1):c.5572A>C (p.Ile1858Leu)	BRCA1 (I1858L +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 55632	NM_007294.4(BRCA1):c.5566C>T (p.Pro1856Ser)	BRCA1 (P1856S +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GLikely benign
Select item 868677	NM_007294.4(BRCA1):c.5563A>G (p.Ile1855Val)	BRCA1 (I1808V +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GUncertain significance
Select item 865013	NM_007294.4(BRCA1):c.5556C>T (p.Thr1852=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign
Select item 441287	NM_007294.4(BRCA1):c.5554A>G (p.Thr1852Ala)	BRCA1 (T1852A +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GUncertain significance
Select item 184500	NM_007294.4(BRCA1):c.5550G>C (p.Leu1850=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 482953	NM_007294.4(BRCA1):c.5547G>A (p.Glu1849=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GLikely benign
Select item 55621	NM_007294.4(BRCA1):c.5538G>A (p.Gln1846=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 481475	NM_007294.4(BRCA1):c.5525T>A (p.Val1842Glu)	BRCA1 (V1842E +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 184051	NM_007294.4(BRCA1):c.5514G>T (p.Val1838=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 55607	NM_007294.4(BRCA1):c.5509T>G (p.Trp1837Gly)	BRCA1 (W1837G +80 more)	Single nucleotide variant (missense variant +2 more)	BRCA1-related cancer predisposition	GPathogenic FDA Recognized database
Select item 55605	NM_007294.4(BRCA1):c.5506G>A (p.Glu1836Lys)	BRCA1 (E1836K +80 more)	Single nucleotide variant (missense variant +2 more)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 182172	NM_007294.4(BRCA1):c.5504G>C (p.Arg1835Pro)	BRCA1 (R1835P +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GUncertain significance
Select item 55604	NM_007294.4(BRCA1):c.5504G>A (p.Arg1835Gln)	BRCA1 (R1835Q +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 55601	NM_007294.4(BRCA1):c.5503C>T (p.Arg1835Ter)	BRCA1 (R1835* +80 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 142865	NM_007294.4(BRCA1):c.5492C>G (p.Pro1831Arg)	BRCA1 (P1831R +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +4 more	GConflicting classifications of pathogenicity
Select item 142395	NM_007294.4(BRCA1):c.5481G>A (p.Met1827Ile)	BRCA1 (M1827I +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GConflicting classifications of pathogenicity
Select item 1631736	NM_007294.4(BRCA1):c.5468-11T>C	BRCA1	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign
Select item 323421	NM_007294.4(BRCA1):c.5466T>C (p.His1822=)	BRCA1 (C694R +9 more)	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 566786	NM_007294.4(BRCA1):c.5444G>C (p.Trp1815Ser)	BRCA1 (W1815S +80 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 55580	NM_007294.4(BRCA1):c.5444G>A (p.Trp1815Ter)	BRCA1 (W1815* +80 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 230363	NM_007294.4(BRCA1):c.5439T>C (p.Asp1813=)	BRCA1 (C685R +9 more)	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 184631	NM_007294.4(BRCA1):c.5430G>A (p.Val1810=)	BRCA1 (A682T +9 more)	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 185996	NM_007294.4(BRCA1):c.5429T>C (p.Val1810Ala)	BRCA1 (V1810A +80 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 55575	NM_007294.4(BRCA1):c.5426T>C (p.Val1809Ala)	BRCA1 (V1809A +80 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 55573	NM_007294.4(BRCA1):c.5425G>T (p.Val1809Phe)	BRCA1 (V1809F +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 186137	NM_007294.4(BRCA1):c.5419A>G (p.Ile1807Val)	BRCA1 (I1807V +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 55570	NM_007294.4(BRCA1):c.5416C>G (p.Pro1806Ala)	BRCA1 (P1806A +90 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 415554	NM_007294.4(BRCA1):c.5415C>T (p.His1805=)	BRCA1 (P677S +9 more)	Single nucleotide variant (synonymous variant +1 more)	not provided +4 more	GLikely benign
Select item 868068	NM_007294.4(BRCA1):c.5407-12C>T	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GLikely benign
Select item 37667	NM_007294.4(BRCA1):c.5406+5G>T	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GPathogenic/Likely pathogenic
Select item 868056	NM_007294.4(BRCA1):c.5406A>G (p.Thr1802=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 252887	NM_007294.4(BRCA1):c.5406A>C (p.Thr1802=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 868055	NM_007294.4(BRCA1):c.5405C>T (p.Thr1802Ile)	BRCA1 (T1802I +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 142834	NM_007294.4(BRCA1):c.5402G>A (p.Gly1801Asp)	BRCA1 (G1801D +79 more)	Single nucleotide variant (missense variant +2 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 868406	NM_007294.4(BRCA1):c.5386T>C (p.Ser1796Pro)	BRCA1 (S1817P +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 795118	NM_007294.4(BRCA1):c.5382G>A (p.Glu1794=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 865677	NM_007294.4(BRCA1):c.5380G>A (p.Glu1794Lys)	BRCA1 (E690K +79 more)	Single nucleotide variant (missense variant +2 more)	BRCA1-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 415572	NM_007294.4(BRCA1):c.5376G>A (p.Val1792=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GLikely benign
Select item 142002	NM_007294.4(BRCA1):c.5371G>T (p.Val1791Leu)	BRCA1 (V1791L +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 55553	NM_007294.4(BRCA1):c.5365G>T (p.Ala1789Ser)	BRCA1 (A1789S +79 more)	Single nucleotide variant (missense variant +2 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 531270	NM_007294.4(BRCA1):c.5347A>G (p.Met1783Val)	BRCA1 (M1783V +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 37658	NM_007294.4(BRCA1):c.5346G>A (p.Trp1782Ter)	BRCA1 (W1782* +79 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 865633	NM_007294.4(BRCA1):c.5335C>A (p.Gln1779Lys)	BRCA1 (Q1732K +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GUncertain significance
Select item 186289	NM_007294.4(BRCA1):c.5334T>C (p.Asp1778=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	not specified +5 more	GBenign/Likely benign
Select item 55539	NM_007294.4(BRCA1):c.5333A>G (p.Asp1778Gly)	BRCA1 (D1778G +79 more)	Single nucleotide variant (missense variant +2 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 55538	NM_007294.4(BRCA1):c.5333-6T>G	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 125831	NM_007294.4(BRCA1):c.5333-8C>T	BRCA1	Single nucleotide variant (intron variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 868335	NM_007294.4(BRCA1):c.5333-13A>G	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 3070131	NM_007294.4(BRCA1):c.5333-30A>G	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 125827	NM_007294.4(BRCA1):c.5332+4A>G	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 55530	NM_007294.4(BRCA1):c.5332G>A (p.Asp1778Asn)	BRCA1 (D1778N +89 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 185660	NM_007294.4(BRCA1):c.5328C>T (p.Pro1776=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 246175	NM_007294.4(BRCA1):c.5327C>A (p.Pro1776His)	BRCA1 (P1776H +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GConflicting classifications of pathogenicity
Select item 91647	NM_007294.4(BRCA1):c.5327C>T (p.Pro1776Leu)	BRCA1 (P1776L +79 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 219830	NM_007294.4(BRCA1):c.5310G>C (p.Gly1770=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 55515	NM_007294.4(BRCA1):c.5310G>A (p.Gly1770=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 216675	NM_007294.4(BRCA1):c.5309G>C (p.Gly1770Ala)	BRCA1 (G1770A +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 55513	NM_007294.4(BRCA1):c.5306A>G (p.Tyr1769Cys)	BRCA1 (Y1769C +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 182097	NM_007294.4(BRCA1):c.5304C>T (p.Cys1768=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 265052	NM_007294.4(BRCA1):c.5296A>G (p.Ile1766Val)	BRCA1 (I1766V +79 more)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 55510	NM_007294.4(BRCA1):c.5291T>C (p.Leu1764Pro)	BRCA1 (L1764P +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 186911	NM_007294.4(BRCA1):c.5280C>A (p.Ile1760=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 55501	NM_007294.4(BRCA1):c.5278-1G>C	BRCA1	Single nucleotide variant (splice acceptor variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic
Select item 389935	NM_007294.4(BRCA1):c.5277+6G>T	BRCA1	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 37654	NM_007294.4(BRCA1):c.5277+1G>A	BRCA1	Single nucleotide variant (splice donor variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 232795	NM_007294.4(BRCA1):c.5274A>G (p.Arg1758=)	BRCA1	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 462666	NM_007294.4(BRCA1):c.5260G>C (p.Glu1754Gln)	BRCA1 (E1754Q +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
Select item 219464	NM_007294.4(BRCA1):c.5225A>G (p.Asn1742Ser)	BRCA1 (N1742S +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 531477	NM_007294.4(BRCA1):c.5211A>G (p.Arg1737=)	BRCA1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 37648	NM_007294.4(BRCA1):c.5207T>C (p.Val1736Ala)	BRCA1 (V1736A +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 491101	NM_007294.4(BRCA1):c.5198A>T (p.Asp1733Val)	BRCA1 (D1733V +79 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 37647	NM_007294.4(BRCA1):c.5194-2A>G	BRCA1	Single nucleotide variant (splice acceptor variant)	Breast and/or ovarian cancer +4 more	GPathogenic/Likely pathogenic
Select item 1581551	NM_007294.4(BRCA1):c.5194-13T>C	BRCA1	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign
Select item 37646	NM_007294.4(BRCA1):c.5191G>T (p.Glu1731Ter)	BRCA1 (E1731* +79 more)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GPathogenic/Likely pathogenic
Select item 37644	NM_007294.4(BRCA1):c.5177_5180del (p.Arg1726fs)	BRCA1 (R1747fs +3 more)	Microsatellite (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 37645	NM_007294.4(BRCA1):c.5179A>T (p.Lys1727Ter)	BRCA1 (K1727* +79 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 136552	NM_007294.4(BRCA1):c.5175A>G (p.Glu1725=)	BRCA1	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 55441	NM_007294.4(BRCA1):c.5165C>T (p.Ser1722Phe)	BRCA1 (S1722F +79 more)	Single nucleotide variant (missense variant +1 more)	not provided +6 more	GPathogenic/Likely pathogenic
Select item 482939	NM_007294.4(BRCA1):c.5163G>A (p.Gln1721=)	BRCA1	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GLikely benign
Select item 184120	NM_007294.4(BRCA1):c.5157G>T (p.Val1719=)	BRCA1	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign
Select item 245993	NM_007294.4(BRCA1):c.5155G>T (p.Val1719Leu)	BRCA1 (V1719L +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
Select item 265051	NM_007294.4(BRCA1):c.5153-6C>T	BRCA1	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 96941	NM_007294.4(BRCA1):c.5153-6C>A	BRCA1	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 867402	NM_007294.4(BRCA1):c.5143A>G (p.Ser1715Gly)	BRCA1 (S1715G +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GUncertain significance
Select item 418578	NM_007294.4(BRCA1):c.5137G>A (p.Val1713Ile)	BRCA1 (V1713I +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 55407	NM_007294.4(BRCA1):c.5123C>A (p.Ala1708Glu)	BRCA1 (A1708E +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 37640	NM_007294.4(BRCA1):c.5123C>T (p.Ala1708Val)	BRCA1 (A1708V +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 55406	NM_007294.4(BRCA1):c.5117G>C (p.Gly1706Ala)	BRCA1 (G1706A +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 37638	NM_007294.4(BRCA1):c.5117G>A (p.Gly1706Glu)	BRCA1 (G1706E +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55402	NM_007294.4(BRCA1):c.5106del (p.Lys1702fs)	BRCA1 (K1655fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 409300	NM_007294.4(BRCA1):c.5101C>A (p.Leu1701Met)	BRCA1 (L1701M +78 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 184204	NM_007294.4(BRCA1):c.5100A>G (p.Thr1700=)	BRCA1	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely benign

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