"Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine"[submitter - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 853644	NM_007294.4(BRCA1):c.5551G>A (p.Asp1851Asn)	BRCA1 (D1802N +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 868637	NM_007294.4(BRCA1):c.5541C>G (p.Cys1847Trp)	BRCA1 (C1847W +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 582037	NM_007294.4(BRCA1):c.5540G>T (p.Cys1847Phe)	BRCA1 (C1847F +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 482930	NM_007294.4(BRCA1):c.5538G>C (p.Gln1846His)	BRCA1 (Q1846H +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 825811	NM_007294.4(BRCA1):c.5536C>A (p.Gln1846Lys)	BRCA1 (Q742K +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 419732	NM_007294.4(BRCA1):c.5531T>C (p.Leu1844Pro)	BRCA1 (L1844P +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 482889	NM_007294.4(BRCA1):c.5530C>A (p.Leu1844Ile)	BRCA1 (L1844I +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 496396	NM_007294.4(BRCA1):c.5528C>T (p.Ala1843Val)	BRCA1 (A1843V +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
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 184981	NM_007294.4(BRCA1):c.5512G>T (p.Val1838Leu)	BRCA1 (V1838L +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
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 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 182171	NM_007294.4(BRCA1):c.5501C>T (p.Thr1834Ile)	BRCA1 (T1834I +80 more)	Single nucleotide variant (missense variant +2 more)	not specified +4 more	GConflicting classifications of pathogenicity
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 844324	NM_007294.4(BRCA1):c.5479A>G (p.Met1827Val)	BRCA1 (M1848V +90 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 55592	NM_007294.4(BRCA1):c.5478G>T (p.Gln1826His)	BRCA1 (Q1826H +90 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 867578	NM_007294.4(BRCA1):c.5471T>C (p.Ile1824Thr)	BRCA1 (I1824T +80 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 141804	NM_007294.4(BRCA1):c.5470A>G (p.Ile1824Val)	BRCA1 (I1824V +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +6 more	GConflicting classifications of pathogenicity
Select item 868959	NM_007294.4(BRCA1):c.5468-4C>T	BRCA1	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
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 628196	NM_007294.4(BRCA1):c.5408G>T (p.Gly1803Val)	BRCA1 (G1803V +80 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 651964	NM_007294.4(BRCA1):c.5407G>T (p.Gly1803Cys)	BRCA1 (G1756C +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 531443	NM_007294.4(BRCA1):c.5407-9G>A	BRCA1	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 628641	NM_007294.4(BRCA1):c.5383C>A (p.Leu1795Ile)	BRCA1 (L1795I +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 240821	NM_007294.4(BRCA1):c.5383C>T (p.Leu1795Phe)	BRCA1 (L1795F +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 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 581900	NM_007294.4(BRCA1):c.5374G>A (p.Val1792Met)	BRCA1 (V1792M +79 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 219775	NM_007294.4(BRCA1):c.5372T>C (p.Val1791Ala)	BRCA1 (V1791A +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 55551	NM_007294.4(BRCA1):c.5363G>A (p.Gly1788Asp)	BRCA1 (G1788D +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GUncertain significance
Select item 141796	NM_007294.4(BRCA1):c.5349G>A (p.Met1783Ile)	BRCA1 (M1783I +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +3 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 489730	NM_007294.4(BRCA1):c.5343A>C (p.Glu1781Asp)	BRCA1 (E1781D +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
Select item 825658	NM_007294.4(BRCA1):c.5335C>G (p.Gln1779Glu)	BRCA1 (Q1779E +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
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 240820	NM_007294.4(BRCA1):c.5332+3A>G	BRCA1	Single nucleotide variant (intron variant)	not provided +3 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 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 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 648860	NM_007294.4(BRCA1):c.5285G>C (p.Arg1762Thr)	BRCA1 (R1762T +79 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 867312	NM_007294.4(BRCA1):c.5277+6G>A	BRCA1	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 867311	NM_007294.4(BRCA1):c.5277+5A>G	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 96947	NM_007294.4(BRCA1):c.5276A>G (p.Lys1759Arg)	BRCA1 (K1759R +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 656220	NM_007294.4(BRCA1):c.5272A>G (p.Arg1758Gly)	BRCA1 (R1758G +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
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 55478	NM_007294.4(BRCA1):c.5245C>G (p.Pro1749Ala)	BRCA1 (P1749A +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 867265	NM_007294.4(BRCA1):c.5239C>G (p.Gln1747Glu)	BRCA1 (Q1747E +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
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 182166	NM_007294.4(BRCA1):c.5186T>A (p.Leu1729Gln)	BRCA1 (L1729Q +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 867779	NM_007294.4(BRCA1):c.5183T>C (p.Met1728Thr)	BRCA1 (M1749T +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 187201	NM_007294.4(BRCA1):c.5177G>T (p.Arg1726Ile)	BRCA1 (R1726I +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 246200	NM_007294.4(BRCA1):c.5172A>C (p.Lys1724Asn)	BRCA1 (K1724N +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 240818	NM_007294.4(BRCA1):c.5161C>G (p.Gln1721Glu)	BRCA1 (Q1721E +79 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
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 187156	NM_007294.4(BRCA1):c.5147A>C (p.Tyr1716Ser)	BRCA1 (Y1716S +78 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 55417	NM_007294.4(BRCA1):c.5145C>A (p.Ser1715Arg)	BRCA1 (S1715R +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GLikely pathogenic
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 801083	NM_007294.4(BRCA1):c.5128G>A (p.Gly1710Arg)	BRCA1 (G1731R +78 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 254642	NM_007294.4(BRCA1):c.5125G>A (p.Gly1709Arg)	BRCA1 (G1709R +78 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
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 41832	NM_007294.4(BRCA1):c.5113C>G (p.Leu1705Val)	BRCA1 (L1705V +78 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
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 867630	NM_007294.4(BRCA1):c.5090G>C (p.Cys1697Ser)	BRCA1 (C1650S +78 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 55369	NM_007294.4(BRCA1):c.5066T>C (p.Met1689Thr)	BRCA1 (M1689T +77 more)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 531444	NM_007294.4(BRCA1):c.5056C>T (p.His1686Tyr)	BRCA1 (H1686Y +77 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +5 more	GConflicting classifications of pathogenicity
Select item 653644	NM_007294.4(BRCA1):c.5050A>T (p.Thr1684Ser)	BRCA1 (T1637S +77 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 216672	NM_007294.4(BRCA1):c.5036T>C (p.Leu1679Pro)	BRCA1 (L1679P +77 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 825381	NM_007294.4(BRCA1):c.5023A>T (p.Thr1675Ser)	BRCA1 (T1628S +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 419497	NM_007294.4(BRCA1):c.5018A>G (p.His1673Arg)	BRCA1 (H1673R +77 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 868917	NM_007294.4(BRCA1):c.5005G>A (p.Ala1669Thr)	BRCA1 (A565T +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 489727	NM_007294.4(BRCA1):c.4999A>G (p.Lys1667Glu)	BRCA1 (K1667E +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 55352	NM_007294.4(BRCA1):c.4997A>G (p.Tyr1666Cys)	BRCA1 (Y1666C +77 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 479204	NM_007294.4(BRCA1):c.4993G>C (p.Val1665Leu)	BRCA1 (V1665L +77 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 479222	NM_007294.4(BRCA1):c.4954A>G (p.Met1652Val)	BRCA1 (M1652V +77 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 865448	NM_007294.4(BRCA1):c.4948A>G (p.Met1650Val)	BRCA1 (M1671V +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 662443	NM_007294.4(BRCA1):c.4942A>G (p.Lys1648Glu)	BRCA1 (K1601E +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 868858	NM_007294.4(BRCA1):c.4935G>T (p.Arg1645Ser)	BRCA1 (R1645S +77 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 41829	NM_007294.4(BRCA1):c.4903G>A (p.Glu1635Lys)	BRCA1 (E1635K +77 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 868384	NM_007294.4(BRCA1):c.4901G>A (p.Arg1634Lys)	BRCA1 (R1634K +77 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 224562	NM_007294.4(BRCA1):c.301+6T>C	BRCA1	Single nucleotide variant (intron variant)	Pancreatic cancer, susceptibility to, 4 +7 more	GConflicting classifications of pathogenicity
Select item 441379	NM_007294.4(BRCA1):c.289A>G (p.Thr97Ala)	BRCA1 (T97A +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 865336	NM_007294.4(BRCA1):c.256C>G (p.Leu86Val)	BRCA1 (L86V +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 865587	NM_007294.4(BRCA1):c.233G>T (p.Arg78Ile)	BRCA1 (R78I +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 54529	NM_007294.4(BRCA1):c.230C>T (p.Thr77Met)	BRCA1 (T77M +4 more)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 54528	NM_007294.4(BRCA1):c.230C>G (p.Thr77Arg)	BRCA1 (T77R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 182123	NM_007294.4(BRCA1):c.216C>G (p.Ser72Arg)	BRCA1 (S72R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 441428	NM_007294.4(BRCA1):c.206C>T (p.Thr69Ile)	BRCA1 (T69I +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 479193	NM_007294.4(BRCA1):c.202A>G (p.Ile68Val)	BRCA1 (I68V +1 more)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 867325	NM_007294.4(BRCA1):c.200A>C (p.Asp67Ala)	BRCA1 (D20A +1 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 820472	NM_007294.4(BRCA1):c.198T>A (p.Asn66Lys)	BRCA1 (N66K +1 more)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GConflicting classifications of pathogenicity
Select item 531303	NM_007294.4(BRCA1):c.193A>G (p.Lys65Glu)	BRCA1 (K65E +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 54389	NM_007294.4(BRCA1):c.189A>T (p.Leu63Phe)	BRCA1 (L63F +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 141093	NM_007294.4(BRCA1):c.179A>G (p.Gln60Arg)	BRCA1 (Q60R +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
Select item 54337	NM_007294.4(BRCA1):c.172C>G (p.Pro58Ala)	BRCA1 (P58A +1 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GConflicting classifications of pathogenicity
Select item 252391	NM_007294.4(BRCA1):c.169G>C (p.Gly57Arg)	BRCA1 (G57R +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 865213	NM_007294.4(BRCA1):c.162G>C (p.Gln54His)	BRCA1 (Q7H +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 867899	NM_007294.4(BRCA1):c.158A>G (p.Asn53Ser)	BRCA1 (N53S +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 54263	NM_007294.4(BRCA1):c.146T>G (p.Leu49Arg)	BRCA1 (L49R +1 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 409343	NM_007294.4(BRCA1):c.135-3T>C	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity

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