"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 141836	NM_000465.4(BARD1):c.2324_2325del (p.Leu775fs)	BARD1 (L262fs +4 more)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 530149	NM_000465.4(BARD1):c.2324T>A (p.Leu775His)	BARD1 (L775H +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 182057	NM_000465.4(BARD1):c.2294A>G (p.Asp765Gly)	BARD1 (D765G +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 928708	NM_000465.4(BARD1):c.2292A>G (p.Ile764Met)	BARD1 (I251M +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 127736	NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr)	BARD1 (I764T +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 127735	NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn)	BARD1 (S761N +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 184291	NM_000465.4(BARD1):c.2280G>A (p.Ser760=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 184883	NM_000465.4(BARD1):c.2255A>G (p.Gln752Arg)	BARD1 (Q752R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 183946	NM_000465.4(BARD1):c.2253G>T (p.Arg751=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +4 more	GBenign/Likely benign
Select item 182055	NM_000465.4(BARD1):c.2248G>A (p.Val750Ile)	BARD1 (V750I +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 820952	NM_000465.4(BARD1):c.2242G>T (p.Glu748Ter)	BARD1 (E297* +4 more)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of breast +2 more	GPathogenic/Likely pathogenic
Select item 232195	NM_000465.4(BARD1):c.2209A>G (p.Ile737Val)	BARD1 (I737V +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 495876	NM_000465.4(BARD1):c.2196C>G (p.Phe732Leu)	BARD1 (F732L +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 917586	NM_000465.4(BARD1):c.2159_2172del (p.Val720fs)	BARD1 (V701fs +4 more)	Deletion (frameshift variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 141050	NM_000465.4(BARD1):c.2161G>A (p.Ala721Thr)	BARD1 (A721T +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 237830	NM_000465.4(BARD1):c.2146A>G (p.Thr716Ala)	BARD1 (T716A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 219805	NM_000465.4(BARD1):c.2145G>A (p.Gln715=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	BARD1-related condition +4 more	GLikely benign
Select item 186019	NM_000465.4(BARD1):c.2137G>A (p.Val713Met)	BARD1 (V713M +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 142456	NM_000465.4(BARD1):c.2129A>T (p.Asp710Val)	BARD1 (D710V +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 187104	NM_000465.4(BARD1):c.2126C>T (p.Pro709Leu)	BARD1 (P709L +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 127730	NM_000465.4(BARD1):c.2116A>G (p.Lys706Glu)	BARD1 (K706E +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 406765	NM_000465.4(BARD1):c.2071C>T (p.Leu691Phe)	BARD1 (L691F +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 406793	NM_000465.4(BARD1):c.2066A>G (p.Asp689Gly)	BARD1 (D689G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 234207	NM_000465.4(BARD1):c.2054A>G (p.His685Arg)	BARD1 (H685R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 479188	NM_000465.4(BARD1):c.1986C>T (p.Leu662=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +2 more	GLikely benign
Select item 237829	NM_000465.4(BARD1):c.1985T>G (p.Leu662Arg)	BARD1 (L662R +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 127727	NM_000465.4(BARD1):c.1977A>G (p.Arg659=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	BARD1-related condition +5 more	GConflicting classifications of pathogenicity
Select item 230212	NM_000465.4(BARD1):c.1973G>A (p.Arg658His)	BARD1 (R658H +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer +6 more	GConflicting classifications of pathogenicity
Select item 246205	NM_000465.4(BARD1):c.1960C>T (p.Pro654Ser)	BARD1 (P654S +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 127725	NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs)	BARD1 (E139fs +4 more)	Duplication (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 142499	NM_000465.4(BARD1):c.1932_1933del (p.Val644_Cys645insTer)	BARD1	Deletion (frameshift variant +1 more)	Familial cancer of breast +3 more	GPathogenic/Likely pathogenic
Select item 142135	NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg)	BARD1 (C645R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 141702	NM_000465.4(BARD1):c.1921C>T (p.Arg641Ter)	BARD1 (R641* +4 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic
Select item 140927	NM_000465.4(BARD1):c.1915T>C (p.Cys639Arg)	BARD1 (C639R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 479130	NM_000465.4(BARD1):c.1912G>A (p.Ala638Thr)	BARD1 (A638T +4 more)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 233368	NM_000465.4(BARD1):c.1904-3C>T	BARD1	Single nucleotide variant (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 185614	NM_000465.4(BARD1):c.1904-5G>A	BARD1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 580468	NM_000465.4(BARD1):c.1883G>A (p.Cys628Tyr)	BARD1 (C628Y +3 more)	Single nucleotide variant (intron variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 141027	NM_000465.4(BARD1):c.1877A>G (p.Asn626Ser)	BARD1 (N626S +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 232127	NM_000465.4(BARD1):c.1872del (p.Leu625fs)	BARD1 (L625fs +3 more)	Deletion (frameshift variant +2 more)	Familial cancer of breast +3 more	GPathogenic/Likely pathogenic
Select item 820168	NM_000465.4(BARD1):c.1840G>A (p.Val614Ile)	BARD1 (V163I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +2 more	GUncertain significance
Select item 142336	NM_000465.4(BARD1):c.1835A>T (p.Asp612Val)	BARD1 (D612V +3 more)	Single nucleotide variant (missense variant +2 more)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 482815	NM_000465.4(BARD1):c.1819GTT[2] (p.Val609del)	BARD1 (V609del +3 more)	Microsatellite (inframe_deletion +2 more)	not provided +4 more	GUncertain significance
Select item 182050	NM_000465.4(BARD1):c.1808C>A (p.Thr603Lys)	BARD1 (T603K +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 127723	NM_000465.4(BARD1):c.1793C>A (p.Thr598Asn)	BARD1 (T598N +3 more)	Single nucleotide variant (missense variant +2 more)	Breast and/or ovarian cancer +4 more	GUncertain significance
Select item 215747	NM_000465.4(BARD1):c.1788A>G (p.Lys596=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	BARD1-related condition +4 more	GBenign/Likely benign
Select item 246505	NM_000465.4(BARD1):c.1772T>A (p.Ile591Asn)	BARD1 (I591N +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance
Select item 185067	NM_000465.4(BARD1):c.1754T>C (p.Leu585Pro)	BARD1 (L585P +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 215746	NM_000465.4(BARD1):c.1731G>A (p.Leu577=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 231254	NM_000465.4(BARD1):c.1729C>T (p.Leu577=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	not specified +2 more	GLikely benign
Select item 231290	NM_000465.4(BARD1):c.1724G>A (p.Ser575Asn)	BARD1 (S575N +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 481422	NM_000465.4(BARD1):c.1721G>T (p.Gly574Val)	BARD1 (G574V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +2 more	GUncertain significance
Select item 127722	NM_000465.4(BARD1):c.1718T>C (p.Ile573Thr)	BARD1 (I573T +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 377556	NM_000465.4(BARD1):c.1704A>G (p.Gly568=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 127721	NM_000465.4(BARD1):c.1694G>A (p.Arg565His)	BARD1 (R565H +3 more)	Single nucleotide variant (missense variant +2 more)	BARD1-related condition +4 more	GConflicting classifications of pathogenicity
Select item 142170	NM_000465.4(BARD1):c.1693C>T (p.Arg565Cys)	BARD1 (R565C +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 490944	NM_000465.4(BARD1):c.1692G>A (p.Gln564=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 127720	NM_000465.4(BARD1):c.1690C>T (p.Gln564Ter)	BARD1 (Q564* +3 more)	Single nucleotide variant (nonsense +2 more)	BARD1-related condition +4 more	GConflicting classifications of pathogenicity
Select item 234117	NM_000465.4(BARD1):c.1689G>A (p.Gly563=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 917574	NM_000465.4(BARD1):c.1678-3C>G	BARD1	Single nucleotide variant (intron variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 127718	NM_000465.4(BARD1):c.1677+5G>A	BARD1	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 220141	NM_000465.4(BARD1):c.1652C>T (p.Ser551Leu)	BARD1 (S551L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GUncertain significance
Select item 141384	NM_000465.4(BARD1):c.1652C>G (p.Ser551Ter)	BARD1 (S551* +3 more)	Single nucleotide variant (nonsense +2 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 423415	NM_000465.4(BARD1):c.1644G>A (p.Lys548=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 184584	NM_000465.4(BARD1):c.1626A>G (p.Leu542=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 490942	NM_000465.4(BARD1):c.1620A>T (p.Lys540Asn)	BARD1 (K540N +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 186171	NM_000465.4(BARD1):c.1613G>A (p.Ser538Asn)	BARD1 (S538N +3 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +3 more	GConflicting classifications of pathogenicity
Select item 388713	NM_000465.4(BARD1):c.1593C>T (p.Val531=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 187625	NM_000465.4(BARD1):c.1586G>A (p.Arg529Gln)	BARD1 (R529Q +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 185032	NM_000465.4(BARD1):c.1585C>T (p.Arg529Trp)	BARD1 (R529W +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 414117	NM_000465.4(BARD1):c.1569-9T>C	BARD1	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1092419	NM_000465.4(BARD1):c.1568+10T>G	BARD1	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 127716	NM_000465.4(BARD1):c.1568T>C (p.Val523Ala)	BARD1 (V523A +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 186247	NM_000465.4(BARD1):c.1554C>T (p.Ala518=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	BARD1-related condition +4 more	GBenign/Likely benign
Select item 479113	NM_000465.4(BARD1):c.1549G>A (p.Gly517Arg)	BARD1 (G517R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +3 more	GUncertain significance
Select item 406736	NM_000465.4(BARD1):c.1544C>G (p.Ser515Cys)	BARD1 (S515C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GUncertain significance
Select item 419324	NM_000465.4(BARD1):c.1518_1519delinsCT (p.Val507Leu)	BARD1 (V507L +1 more)	Indel (non-coding transcript variant +2 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 182028	NM_000465.4(BARD1):c.1515G>T (p.Gly505=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	BARD1-related condition +3 more	GBenign/Likely benign
Select item 184616	NM_000465.4(BARD1):c.1491A>G (p.Pro497=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	BARD1-related condition +4 more	GBenign/Likely benign
Select item 385318	NM_000465.4(BARD1):c.1479A>G (p.Gln493=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	not specified +4 more	GLikely benign
Select item 928639	NM_000465.4(BARD1):c.1470C>G (p.Thr490=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 1027599	NM_000465.4(BARD1):c.1467C>T (p.Thr489=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Familial cancer of breast +2 more	GLikely benign
Select item 917787	NM_000465.4(BARD1):c.1461G>T (p.Val487=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 628208	NM_000465.4(BARD1):c.1457T>C (p.Leu486Ser)	BARD1 (L486S +1 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 495874	NM_000465.4(BARD1):c.1443C>T (p.Leu481=)	BARD1	Single nucleotide variant (intron variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 186788	NM_000465.4(BARD1):c.1438T>C (p.Leu480=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 141739	NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser)	BARD1 (N470S +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 232097	NM_000465.4(BARD1):c.1361C>T (p.Pro454Leu)	BARD1 (P454L +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 182033	NM_000465.4(BARD1):c.1360C>G (p.Pro454Ala)	BARD1 (P454A +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 233380	NM_000465.4(BARD1):c.1353A>T (p.Gly451=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 233414	NM_000465.4(BARD1):c.1349dup (p.Asn450fs)	BARD1 (N450fs +1 more)	Duplication (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 182027	NM_000465.4(BARD1):c.1347A>G (p.Gln449=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	BARD1-related condition +5 more	GConflicting classifications of pathogenicity
Select item 182046	NM_000465.4(BARD1):c.1339C>G (p.Leu447Val)	BARD1 (L447V +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 182045	NM_000465.4(BARD1):c.1325C>T (p.Pro442Leu)	BARD1 (P442L +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 232477	NM_000465.4(BARD1):c.1311T>C (p.Ile437=)	BARD1	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 406766	NM_000465.4(BARD1):c.1309A>G (p.Ile437Val)	BARD1 (I437V +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 485306	NM_000465.4(BARD1):c.1294C>T (p.Leu432Phe)	BARD1 (L432F +1 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 495873	NM_000465.4(BARD1):c.1289C>T (p.Thr430Ile)	BARD1 (T430I +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 479125	NM_000465.4(BARD1):c.1270A>G (p.Arg424Gly)	BARD1 (R424G +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 231816	NM_000465.4(BARD1):c.1265T>C (p.Val422Ala)	BARD1 (V422A +1 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +3 more	GUncertain significance

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