"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "BARD1"[ - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 2866

<< First< Prev

Page of 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 951555	NM_000465.4(BARD1):c.2330_*684del (p.Ser777fs)	BARD1 (S264fs +4 more)	Deletion (frameshift variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 665652	NC_000002.12:g.(?_214728666)_(214745864_?)del	LOC129935541, BARD1 +1 more	Deletion	Familial cancer of breast	GPathogenic
Select item 660670	NC_000002.12:g.(?_214728666)_(214809579_?)del	BARD1, LOC129935540 +3 more	Deletion	Familial cancer of breast	GPathogenic
Select item 655756	NC_000002.12:g.(?_214728666)_(214730518_?)del	BARD1	Deletion	Familial cancer of breast	GLikely pathogenic
Select item 655226	NC_000002.12:g.(?_214728666)_(214797127_?)del	BARD1, LOC129935540 +1 more	Deletion	Familial cancer of breast	GPathogenic
Select item 649054	NC_000002.11:g.(?_215593390)_(215634046_?)dup	BARD1, LOC129935540 +1 more	Duplication	Familial cancer of breast	GUncertain significance
Select item 584246	NC_000002.11:g.(?_215593390)_(215674303_?)dup	BARD1, LOC129935540 +3 more	Duplication	Familial cancer of breast	GUncertain significance
Select item 583721	NC_000002.11:g.(?_215593394)_(215634042_?)dup	BARD1, LOC129935540 +1 more	Duplication	Familial cancer of breast	GUncertain significance
Select item 460645	NC_000002.11:g.(?_215593394)_(215674299_?)dup	BARD1, LOC129935540 +3 more	Duplication	Familial cancer of breast	GUncertain significance
Select item 460644	NC_000002.12:g.(?_214728670)_(214781515_?)del	BARD1, LOC129935540 +1 more	Deletion	Familial cancer of breast	GPathogenic
Select item 216434	NM_000465.3(BARD1):c.1315-?_*(1_?)dup	BARD1, LOC129935540 +1 more	Duplication	Familial cancer of breast	GUncertain significance
Select item 919193	NM_000465.4(BARD1):c.2334A>G (p.Ter778Trp)	BARD1	Single nucleotide variant (stop lost +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 628819	NM_000465.4(BARD1):c.2333G>C (p.Ter778Ser)	BARD1	Single nucleotide variant (stop lost +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 231736	NM_000465.4(BARD1):c.2333G>A (p.Ter778=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1660587	NM_000465.4(BARD1):c.2331C>T (p.Ser777=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 2893954	NM_000465.4(BARD1):c.2330G>A (p.Ser777Asn)	BARD1 (S758N +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 530166	NM_000465.4(BARD1):c.2329A>C (p.Ser777Arg)	BARD1 (S777R +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 216443	NM_000465.4(BARD1):c.2328C>T (p.Asp776=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 1518744	NM_000465.4(BARD1):c.2326G>C (p.Asp776His)	BARD1 (D263H +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
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)	not provided +3 more	GUncertain significance
Select item 530032	NM_000465.4(BARD1):c.2323C>T (p.Leu775Phe)	BARD1 (L775F +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GConflicting classifications of pathogenicity
Select item 1789600	NM_000465.4(BARD1):c.2322T>C (p.Pro774=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +1 more	GBenign/Likely benign
Select item 578473	NM_000465.4(BARD1):c.2321C>T (p.Pro774Leu)	BARD1 (P774L +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1620214	NM_000465.4(BARD1):c.2319T>C (p.Leu773=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 629449	NM_000465.4(BARD1):c.2318T>C (p.Leu773Pro)	BARD1 (L773P +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 1434377	NM_000465.4(BARD1):c.2317C>G (p.Leu773Val)	BARD1 (L322V +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 485319	NM_000465.4(BARD1):c.2317C>T (p.Leu773Phe)	BARD1 (L773F +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 530225	NM_000465.4(BARD1):c.2316G>A (p.Leu772=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 2808827	NM_000465.4(BARD1):c.2313G>C (p.Glu771Asp)	BARD1 (E771D +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 387618	NM_000465.4(BARD1):c.2313G>A (p.Glu771=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +2 more	GBenign/Likely benign
Select item 1789448	NM_000465.4(BARD1):c.2311G>C (p.Glu771Gln)	BARD1 (E752Q +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GConflicting classifications of pathogenicity
Select item 2761436	NM_000465.4(BARD1):c.2310T>C (p.Phe770=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GLikely benign
Select item 967350	NM_000465.4(BARD1):c.2309T>G (p.Phe770Cys)	BARD1 (F257C +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 2864357	NM_000465.4(BARD1):c.2307C>G (p.Ser769=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GLikely benign
Select item 1013922	NM_000465.4(BARD1):c.2307del (p.Phe770fs)	BARD1 (F257fs +4 more)	Deletion (frameshift variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 414129	NM_000465.4(BARD1):c.2307C>T (p.Ser769=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +1 more	GBenign/Likely benign
Select item 1956153	NM_000465.4(BARD1):c.2306C>T (p.Ser769Phe)	BARD1 (S318F +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 182058	NM_000465.4(BARD1):c.2306C>G (p.Ser769Cys)	BARD1 (S769C +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 481365	NM_000465.4(BARD1):c.2304G>A (p.Met768Ile)	BARD1 (M768I +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 530123	NM_000465.4(BARD1):c.2303T>C (p.Met768Thr)	BARD1 (M768T +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 2812826	NM_000465.4(BARD1):c.2301G>C (p.Val767=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GBenign/Likely benign
Select item 1331809	NM_000465.4(BARD1):c.2301G>A (p.Val767=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +1 more	GBenign/Likely benign
Select item 230523	NM_000465.4(BARD1):c.2300_2301del (p.Val767fs)	BARD1 (V254fs +4 more)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 1521461	NM_000465.4(BARD1):c.2299G>A (p.Val767Met)	BARD1 (V316M +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 479124	NM_000465.4(BARD1):c.2299G>T (p.Val767Leu)	BARD1 (V767L +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GConflicting classifications of pathogenicity
Select item 1010066	NM_000465.4(BARD1):c.2297G>A (p.Cys766Tyr)	BARD1 (C253Y +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2765043	NM_000465.4(BARD1):c.2296T>G (p.Cys766Gly)	BARD1 (C766G +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 2849404	NM_000465.4(BARD1):c.2295C>G (p.Asp765Glu)	BARD1 (D252E +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 1620215	NM_000465.4(BARD1):c.2295C>T (p.Asp765=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GBenign/Likely benign
Select item 2203255	NM_000465.4(BARD1):c.2291_2294del (p.Ile764fs)	BARD1 (I294fs +4 more)	Deletion (frameshift variant +1 more)	Familial cancer of breast +1 more	GLikely pathogenic
Select item 182057	NM_000465.4(BARD1):c.2294A>G (p.Asp765Gly)	BARD1 (D765G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 821018	NM_000465.4(BARD1):c.2293G>A (p.Asp765Asn)	BARD1 (D252N +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GConflicting classifications of pathogenicity
Select item 2850843	NM_000465.4(BARD1):c.2292A>C (p.Ile764=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GLikely benign
Select item 127736	NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr)	BARD1 (I764T +4 more)	Single nucleotide variant (missense variant +1 more)	BARD1-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 530103	NM_000465.4(BARD1):c.2290A>G (p.Ile764Val)	BARD1 (I764V +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 2421054	NM_000465.4(BARD1):c.2286G>C (p.Trp762Cys)	BARD1 (W249C +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2036678	NM_000465.4(BARD1):c.2286G>A (p.Trp762Ter)	BARD1 (W762* +4 more)	Single nucleotide variant (nonsense +1 more)	Familial cancer of breast	GLikely pathogenic
Select item 237832	NM_000465.4(BARD1):c.2284T>C (p.Trp762Arg)	BARD1 (W762R +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 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 645078	NM_000465.4(BARD1):c.2281A>G (p.Ser761Gly)	BARD1 (S248G +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 707786	NM_000465.4(BARD1):c.2280G>C (p.Ser760=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 184291	NM_000465.4(BARD1):c.2280G>A (p.Ser760=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +3 more	GConflicting classifications of pathogenicity
Select item 934257	NM_000465.4(BARD1):c.2279C>A (p.Ser760Ter)	BARD1 (S290* +4 more)	Single nucleotide variant (nonsense +1 more)	Familial cancer of breast	GLikely pathogenic
Select item 479129	NM_000465.4(BARD1):c.2279C>T (p.Ser760Leu)	BARD1 (S760L +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 1019526	NM_000465.4(BARD1):c.2278T>C (p.Ser760Pro)	BARD1 (S247P +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 482796	NM_000465.4(BARD1):c.2277T>C (p.Pro759=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast +1 more	GBenign/Likely benign
Select item 485326	NM_000465.4(BARD1):c.2275C>G (p.Pro759Ala)	BARD1 (P759A +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 482803	NM_000465.4(BARD1):c.2275C>T (p.Pro759Ser)	BARD1 (P759S +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 1466571	NM_000465.4(BARD1):c.2273C>T (p.Ala758Val)	BARD1 (A245V +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 652706	NM_000465.4(BARD1):c.2273C>A (p.Ala758Asp)	BARD1 (A288D +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 820999	NM_000465.4(BARD1):c.2272G>A (p.Ala758Thr)	BARD1 (A288T +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 820927	NM_000465.4(BARD1):c.2272G>T (p.Ala758Ser)	BARD1 (A288S +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 216442	NM_000465.4(BARD1):c.2272G>C (p.Ala758Pro)	BARD1 (A758P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 761668	NM_000465.4(BARD1):c.2271G>A (p.Lys757=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 423972	NM_000465.4(BARD1):c.2271G>T (p.Lys757Asn)	BARD1 (K757N +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 820985	NM_000465.4(BARD1):c.2268G>C (p.Trp756Cys)	BARD1 (W286C +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 185366	NM_000465.4(BARD1):c.2268G>A (p.Trp756Ter)	BARD1 (W756* +4 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 863791	NM_000465.4(BARD1):c.2267G>A (p.Trp756Ter)	BARD1 (W286* +4 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 1657309	NM_000465.4(BARD1):c.2265C>A (p.Val755=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Familial cancer of breast	GLikely benign
Select item 820983	NM_000465.4(BARD1):c.2265C>G (p.Val755=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2813308	NM_000465.4(BARD1):c.2264T>G (p.Val755Gly)	BARD1 (V736G +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 530080	NM_000465.4(BARD1):c.2264T>C (p.Val755Ala)	BARD1 (V755A +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 231229	NM_000465.4(BARD1):c.2263G>A (p.Val755Ile)	BARD1 (V755I +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 646575	NM_000465.4(BARD1):c.2261_2262del (p.Lys754fs)	BARD1 (K735fs +4 more)	Deletion (frameshift variant +1 more)	Familial cancer of breast +1 more	GLikely pathogenic
Select item 460741	NM_000465.4(BARD1):c.2262A>G (p.Lys754=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 2861853	NM_000465.4(BARD1):c.2261A>C (p.Lys754Thr)	BARD1 (K735T +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 758415	NM_000465.4(BARD1):c.2259C>A (p.Gly753=)	BARD1	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely benign
Select item 381945	NM_000465.4(BARD1):c.2259C>T (p.Gly753=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 649553	NM_000465.4(BARD1):c.2258G>T (p.Gly753Val)	BARD1 (G240V +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1365760	NM_000465.4(BARD1):c.2257G>T (p.Gly753Cys)	BARD1 (G240C +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 187014	NM_000465.4(BARD1):c.2257G>A (p.Gly753Ser)	BARD1 (G753S +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 839567	NM_000465.4(BARD1):c.2256G>C (p.Gln752His)	BARD1 (Q239H +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 959252	NM_000465.4(BARD1):c.2255A>C (p.Gln752Pro)	BARD1 (Q282P +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
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	GConflicting classifications of pathogenicity
Select item 949838	NM_000465.4(BARD1):c.2254C>G (p.Gln752Glu)	BARD1 (Q282E +4 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 186572	NM_000465.4(BARD1):c.2253G>A (p.Arg751=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 183946	NM_000465.4(BARD1):c.2253G>T (p.Arg751=)	BARD1	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 479151	NM_000465.4(BARD1):c.2252G>C (p.Arg751Pro)	BARD1 (R751P +4 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 142117	NM_000465.4(BARD1):c.2252G>A (p.Arg751Gln)	BARD1 (R751Q +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance

<< First< Prev

Page of 29