C2676676[trait identifier] AND "Sharing Clinical Reports Project (SCRP - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 935

<< First< Prev

Page of 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9342	NM_000059.4(BRCA2):c.658_659del (p.Val220fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 9326	NM_000059.4(BRCA2):c.771_775del (p.Asn257fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37736	NM_000059.4(BRCA2):c.1296_1297del (p.Asn433fs)	BRCA2 (N433fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37762	NM_000059.4(BRCA2):c.1813dup (p.Ile605fs)	BRCA2 (I605fs)	Duplication (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 9322	NM_000059.3(BRCA2):c.2808_2811del (p.Ala938Profs)	BRCA2 (A938fs)	Deletion	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 51421	NM_000059.4(BRCA2):c.3199del (p.Thr1067fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37856	NM_000059.4(BRCA2):c.3744_3747del (p.Ser1248fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 51599	NM_000059.4(BRCA2):c.4111C>T (p.Gln1371Ter)	BRCA2 (Q1371*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37935	NM_000059.4(BRCA2):c.4936_4939del (p.Glu1646fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37939	NM_000059.4(BRCA2):c.5035del (p.Thr1679fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37943	NM_000059.4(BRCA2):c.5073dup (p.Trp1692fs)	BRCA2 (W1692fs)	Duplication	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 51775	NM_000059.4(BRCA2):c.5130_5133del (p.Asp1709_Tyr1710insTer)	BRCA2	Deletion (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37951	NM_000059.4(BRCA2):c.5213_5216del (p.Thr1738fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37954	NM_000059.4(BRCA2):c.5238dup (p.Asn1747Ter)	BRCA2 (N1747*)	Duplication (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37960	NM_000059.4(BRCA2):c.5351dup (p.Asn1784fs)	BRCA2 (N1784fs)	Duplication (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 37989	NM_000059.4(BRCA2):c.5682C>G (p.Tyr1894Ter)	BRCA2 (Y1894*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 9320	NM_000059.4(BRCA2):c.5722_5723del (p.Leu1908fs)	BRCA2 (L1908fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38001	NM_000059.4(BRCA2):c.5851_5854del (p.Ser1951fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38043	NM_000059.4(BRCA2):c.6405_6409del (p.Asn2135fs)	BRCA2 (N2135fs)	Deletion	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52100	NM_000059.4(BRCA2):c.6445_6446del (p.Ser2148_Ile2149insTer)	BRCA2	Deletion (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38047	NM_000059.4(BRCA2):c.6468_6469del (p.Gln2157fs)	BRCA2 (Q2157fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38059	NM_000059.4(BRCA2):c.6641dup (p.Tyr2215fs)	BRCA2 (Y2215fs)	Duplication (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52241	NM_000059.4(BRCA2):c.7007G>C (p.Arg2336Pro)	BRCA2 (R2336P)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +6 more	GPathogenic
Select item 38082	NM_000059.4(BRCA2):c.7069_7070del (p.Leu2357fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52298	NM_000059.4(BRCA2):c.7251_7252del (p.His2417fs)	BRCA2 (H2417fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52353	NM_000059.4(BRCA2):c.7558C>T (p.Arg2520Ter)	BRCA2 (R2520*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52418	NM_000059.4(BRCA2):c.7806-2A>G	BRCA2	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 96864	NM_000059.4(BRCA2):c.7985C>A (p.Thr2662Lys)	BRCA2 (T2662K)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 52471	NM_000059.4(BRCA2):c.8009C>T (p.Ser2670Leu)	BRCA2 (S2670L)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 1 +11 more	GPathogenic/Likely pathogenic
Select item 38149	NM_000059.4(BRCA2):c.8297del (p.Thr2766fs)	BRCA2	Deletion (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38183	NM_000059.4(BRCA2):c.8755-1G>A	BRCA2	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 52694	NM_000059.4(BRCA2):c.8878C>T (p.Gln2960Ter)	BRCA2 (Q2960*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38208	NM_000059.4(BRCA2):c.9097dup (p.Thr3033fs)	BRCA2 (T3033fs)	Duplication (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38215	NM_000059.4(BRCA2):c.9117G>A (p.Pro3039=)	BRCA2	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic FDA Recognized database
Select item 52763	NM_000059.4(BRCA2):c.9154C>T (p.Arg3052Trp)	BRCA2 (R3052W)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 9347	NM_000059.4(BRCA2):c.9196C>T (p.Gln3066Ter)	BRCA2 (Q3066*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 38229	NM_000059.4(BRCA2):c.9294C>G (p.Tyr3098Ter)	BRCA2 (Y3098*)	Single nucleotide variant (nonsense)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
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
Select item 38240	NM_000059.4(BRCA2):c.9435_9436del (p.Ser3147fs)	BRCA2 (S3147fs)	Microsatellite (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 96891	NM_007294.4(BRCA1):c.103_106del	BRCA1	Deletion (3 prime UTR variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 187111	NM_007294.4(BRCA1):c.5571_5579del (p.Gln1857_Pro1859del)	BRCA1	Deletion (inframe_indel +3 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 37683	NM_007294.4(BRCA1):c.5578dup (p.His1860fs)	BRCA1 (H756fs +3 more)	Duplication (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 37682	NM_007294.4(BRCA1):c.5565_5573del (p.Gln1857_Pro1859del)	BRCA1	Deletion (inframe_indel +3 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 55632	NM_007294.4(BRCA1):c.5566C>T (p.Pro1856Ser)	BRCA1 (P1856S +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 55631	NM_007294.4(BRCA1):c.5561T>C (p.Leu1854Pro)	BRCA1 (L1854P +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 55628	NM_007294.4(BRCA1):c.5558dup (p.Tyr1853Ter)	BRCA1 (Y1853* +3 more)	Duplication (frameshift variant +3 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55622	NM_007294.4(BRCA1):c.5541C>A (p.Cys1847Ter)	BRCA1 (C1847* +80 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55615	NM_007294.4(BRCA1):c.5531T>G (p.Leu1844Arg)	BRCA1 (L1844R +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 37681	NM_007294.4(BRCA1):c.5521A>C (p.Ser1841Arg)	BRCA1 (S1841R +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 91656	NM_007294.4(BRCA1):c.5516T>C (p.Leu1839Ser)	BRCA1 (L1839S +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55611	NM_007294.4(BRCA1):c.5513T>A (p.Val1838Glu)	BRCA1 (V1838E +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 37680	NM_007294.4(BRCA1):c.5511G>T (p.Trp1837Cys)	BRCA1 (W1837C +80 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 37679	NM_007294.4(BRCA1):c.5509T>C (p.Trp1837Arg)	BRCA1 (W1837R +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55604	NM_007294.4(BRCA1):c.5504G>A (p.Arg1835Gln)	BRCA1 (R1835Q +80 more)	Single nucleotide variant (missense variant +2 more)	Breast neoplasm +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 55598	NM_007294.4(BRCA1):c.5497G>A (p.Val1833Met)	BRCA1 (V1833M +80 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +4 more	GPathogenic/Likely pathogenic
Select item 96952	NM_007294.4(BRCA1):c.5478_5479dup (p.Met1827fs)	BRCA1 (M1848fs +4 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 91654	NM_007294.4(BRCA1):c.5473G>A (p.Gly1825Arg)	BRCA1 (G1825R +90 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 91653	NM_007294.4(BRCA1):c.5468-2A>G	BRCA1	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 91652	NM_007294.4(BRCA1):c.5468-10_5468-9del	BRCA1	Microsatellite (intron variant)	Hereditary breast ovarian cancer syndrome +3 more	GBenign/Likely benign
Select item 91651	NM_007294.4(BRCA1):c.5467+8G>A	BRCA1	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 37673	NM_007294.4(BRCA1):c.5467+1G>A	BRCA1	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 91650	NM_007294.4(BRCA1):c.5458G>A (p.Gly1820Ser)	BRCA1 (G1820S +90 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +3 more	GConflicting classifications of pathogenicity
Select item 55585	NM_007294.4(BRCA1):c.5456A>G (p.Asn1819Ser)	BRCA1 (N1819S +80 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 37672	NM_007294.4(BRCA1):c.5453A>G (p.Asp1818Gly)	BRCA1 (D1818G +80 more)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +3 more	GPathogenic/Likely pathogenic
Select item 55581	NM_007294.4(BRCA1):c.5445G>A (p.Trp1815Ter)	BRCA1 (W1815* +90 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
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 37670	NM_007294.4(BRCA1):c.5434C>G (p.Pro1812Ala)	BRCA1 (P1812A +90 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 55578	NM_007294.4(BRCA1):c.5432A>G (p.Gln1811Arg)	BRCA1 (Q1811R +80 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +3 more	GLikely pathogenic
Select item 55574	NM_007294.4(BRCA1):c.5425_5430del (p.Val1809_Val1810del)	BRCA1	Deletion (inframe_indel +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 37669	NM_007294.4(BRCA1):c.5417del (p.Pro1806fs)	BRCA1 (P1759fs +4 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55568	NM_007294.4(BRCA1):c.5411T>A (p.Val1804Asp)	BRCA1 (V1804D +90 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 37668	NM_007294.4(BRCA1):c.5408G>C (p.Gly1803Ala)	BRCA1 (G1803A +80 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 96950	NM_007294.4(BRCA1):c.5407-10G>A	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 156197	NM_007294.4(BRCA1):c.5407-16C>T	BRCA1	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 55566	NM_007294.4(BRCA1):c.5406+7A>G	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 55564	NM_007294.4(BRCA1):c.5406+5G>A	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 37667	NM_007294.4(BRCA1):c.5406+5G>T	BRCA1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 37666	NM_007294.4(BRCA1):c.5406+1G>A	BRCA1	Single nucleotide variant (splice donor variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
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 156196	NM_007294.4(BRCA1):c.5401G>A (p.Gly1801Ser)	BRCA1 (G1801S +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 252886	NM_007294.4(BRCA1):c.5390C>T (p.Ser1797Leu)	BRCA1 (S1797L +79 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 37663	NM_007294.4(BRCA1):c.5387C>A (p.Ser1796Ter)	BRCA1 (S1796* +79 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 37662	NM_007294.4(BRCA1):c.5386del (p.Ser1796fs)	BRCA1 (S1749fs +3 more)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
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 37660	NM_007294.4(BRCA1):c.5363G>T (p.Gly1788Val)	BRCA1 (G1788V +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55548	NM_007294.4(BRCA1):c.5359T>A (p.Cys1787Ser)	BRCA1 (C1787S +79 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	Gnot provided
Select item 91649	NM_007294.4(BRCA1):c.5357T>C (p.Leu1786Pro)	BRCA1 (L1786P +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GConflicting classifications of pathogenicity
Select item 55546	NM_007294.4(BRCA1):c.5353C>T (p.Gln1785Ter)	BRCA1 (Q1785* +79 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 37659	NM_007294.4(BRCA1):c.5348T>C (p.Met1783Thr)	BRCA1 (M1783T +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer +6 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 55542	NM_007294.4(BRCA1):c.5341G>T (p.Glu1781Ter)	BRCA1 (E1781* +79 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 96949	NM_007294.4(BRCA1):c.5339T>G (p.Leu1780Arg)	BRCA1 (L1780R +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 37657	NM_007294.4(BRCA1):c.5335del (p.Gln1779fs)	BRCA1 (Q1732fs +3 more)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 55539	NM_007294.4(BRCA1):c.5333A>G (p.Asp1778Gly)	BRCA1 (D1778G +79 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 55536	NM_007294.4(BRCA1):c.5333-2A>T	BRCA1	Single nucleotide variant (splice acceptor variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 1 +1 more	GPathogenic/Likely pathogenic
Select item 125831	NM_007294.4(BRCA1):c.5333-8C>T	BRCA1	Single nucleotide variant (intron variant)	BRCA1-related condition +5 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)	Breast-ovarian cancer, familial, susceptibility to, 1 +3 more	GPathogenic/Likely pathogenic
Select item 91648	NM_007294.4(BRCA1):c.5330C>T (p.Thr1777Ile)	BRCA1 (T1777I +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 91647	NM_007294.4(BRCA1):c.5327C>T (p.Pro1776Leu)	BRCA1 (P1776L +79 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity

<< First< Prev

Page of 10