"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CDC73"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 286328	NM_024529.5(CDC73):c.-4dup	CDC73	Duplication (5 prime UTR variant)	Hyperparathyroidism 2 with jaw tumors +5 more	GConflicting classifications of pathogenicity
Select item 647462	NC_000001.11:g.(?_193122191)_(193250722_?)del	B3GALT2, CDC73 +2 more	Deletion	Parathyroid carcinoma	GPathogenic
Select item 642042	NC_000001.10:g.(?_193091321)_(193219852_?)dup	B3GALT2, CDC73 +2 more	Duplication	Parathyroid carcinoma	GUncertain significance
Select item 583491	NC_000001.11:g.(?_193122191)_(193122341_?)del	CDC73	Deletion	Parathyroid carcinoma	GPathogenic
Select item 2818838	NM_024529.5(CDC73):c.2dup (p.Met1fs)	CDC73 (M1fs)	Duplication (frameshift variant +1 more)	Parathyroid carcinoma	GPathogenic
Select item 582687	NM_024529.5(CDC73):c.1A>G (p.Met1Val)	CDC73 (M1V)	Single nucleotide variant (missense variant +1 more)	Parathyroid carcinoma	GPathogenic
Select item 403893	NM_024529.5(CDC73):c.4del (p.Ala2fs)	CDC73 (A2fs)	Deletion (frameshift variant +1 more)	Parathyroid carcinoma	GPathogenic
Select item 939836	NM_024529.5(CDC73):c.7dup (p.Asp3fs)	CDC73 (D3fs)	Duplication (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 855632	NM_024529.5(CDC73):c.8A>G (p.Asp3Gly)	CDC73 (D3G)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +4 more	GUncertain significance
Select item 1144136	NM_024529.5(CDC73):c.9C>T (p.Asp3=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 579524	NM_024529.5(CDC73):c.12_31dup (p.Tyr11fs)	CDC73 (Y11fs)	Duplication (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 1069972	NM_024529.5(CDC73):c.10del (p.Val4fs)	CDC73 (V4fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 857725	NM_024529.5(CDC73):c.10G>C (p.Val4Leu)	CDC73 (V4L)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1617882	NM_024529.5(CDC73):c.12G>C (p.Val4=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 1425314	NM_024529.5(CDC73):c.13C>T (p.Leu5Phe)	CDC73 (L5F)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1127785	NM_024529.5(CDC73):c.15T>G (p.Leu5=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2045701	NM_024529.5(CDC73):c.16A>G (p.Ser6Gly)	CDC73 (S6G)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2760655	NM_024529.5(CDC73):c.17del (p.Ser6fs)	CDC73 (S6fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 2197389	NM_024529.5(CDC73):c.17G>T (p.Ser6Ile)	CDC73 (S6I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2809114	NM_024529.5(CDC73):c.18C>A (p.Ser6Arg)	CDC73 (S6R)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1579078	NM_024529.5(CDC73):c.18C>T (p.Ser6=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 1093894	NM_024529.5(CDC73):c.21C>G (p.Val7=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 699954	NM_024529.5(CDC73):c.21C>T (p.Val7=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1554999	NM_024529.5(CDC73):c.22C>T (p.Leu8=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 3268	NM_024529.5(CDC73):c.25C>T (p.Arg9Ter)	CDC73 (R9*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 1719933	NM_024529.5(CDC73):c.26G>C (p.Arg9Pro)	CDC73 (R9P)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +1 more	GUncertain significance
Select item 1404245	NM_024529.5(CDC73):c.26G>A (p.Arg9Gln)	CDC73 (R9Q)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 412620	NM_024529.5(CDC73):c.27A>G (p.Arg9=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2702399	NM_024529.5(CDC73):c.28C>T (p.Gln10Ter)	CDC73 (Q10*)	Single nucleotide variant (nonsense)	Parathyroid carcinoma	GPathogenic
Select item 2770312	NM_024529.5(CDC73):c.29A>G (p.Gln10Arg)	CDC73 (Q10R)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1691936	NM_024529.5(CDC73):c.29A>T (p.Gln10Leu)	CDC73 (Q10L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1650076	NM_024529.5(CDC73):c.30G>A (p.Gln10=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2734057	NM_024529.5(CDC73):c.35_41del (p.Asn12fs)	CDC73 (N12fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 241495	NM_024529.5(CDC73):c.33C>T (p.Tyr11=)	CDC73	Single nucleotide variant (synonymous variant)	Hyperparathyroidism 1 +4 more	GBenign/Likely benign
Select item 2869482	NM_024529.5(CDC73):c.34A>C (p.Asn12His)	CDC73 (N12H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2847407	NM_024529.5(CDC73):c.34A>G (p.Asn12Asp)	CDC73 (N12D)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 706738	NM_024529.5(CDC73):c.36C>T (p.Asn12=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2095086	NM_024529.5(CDC73):c.37A>T (p.Ile13Phe)	CDC73 (I13F)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1016680	NM_024529.5(CDC73):c.37A>G (p.Ile13Val)	CDC73 (I13V)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2040186	NM_024529.5(CDC73):c.39C>G (p.Ile13Met)	CDC73 (I13M)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1738633	NM_024529.5(CDC73):c.41A>C (p.Gln14Pro)	CDC73 (Q14P)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +1 more	GUncertain significance
Select item 838171	NM_024529.5(CDC73):c.41A>G (p.Gln14Arg)	CDC73 (Q14R)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +1 more	GUncertain significance
Select item 659234	NM_024529.5(CDC73):c.43AAG[1] (p.Lys16del)	CDC73 (K16del)	Microsatellite (inframe_deletion)	Parathyroid carcinoma	GUncertain significance
Select item 2758093	NM_024529.5(CDC73):c.43A>T (p.Lys15Ter)	CDC73 (K15*)	Single nucleotide variant (nonsense)	Parathyroid carcinoma	GPathogenic
Select item 1010100	NM_024529.5(CDC73):c.46A>G (p.Lys16Glu)	CDC73 (K16E)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1743172	NM_024529.5(CDC73):c.47A>G (p.Lys16Arg)	CDC73 (K16R)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +2 more	GUncertain significance
Select item 1720638	NM_024529.5(CDC73):c.48G>T (p.Lys16Asn)	CDC73 (K16N)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1078985	NM_024529.5(CDC73):c.48G>A (p.Lys16=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 2024534	NM_024529.5(CDC73):c.52A>G (p.Ile18Val)	CDC73 (I18V)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2820972	NM_024529.5(CDC73):c.53T>C (p.Ile18Thr)	CDC73 (I18T)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 567635	NM_024529.5(CDC73):c.53_54del (p.Ile18fs)	CDC73 (I18fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 2032515	NM_024529.5(CDC73):c.56_57del (p.Val19fs)	CDC73 (V19fs)	Microsatellite (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 1673371	NM_024529.5(CDC73):c.54T>C (p.Ile18=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 403884	NM_024529.5(CDC73):c.55G>A (p.Val19Met)	CDC73 (V19M)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +1 more	GUncertain significance
Select item 751210	NM_024529.5(CDC73):c.60G>A (p.Val20=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 3005321	NM_024529.5(CDC73):c.63G>T (p.Lys21Asn)	CDC73 (K21N)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 967087	NM_024529.5(CDC73):c.64G>T (p.Gly22Ter)	CDC73 (G22*)	Single nucleotide variant (nonsense)	Parathyroid carcinoma	GPathogenic
Select item 2122590	NM_024529.5(CDC73):c.65G>A (p.Gly22Glu)	CDC73 (G22E)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 856182	NM_024529.5(CDC73):c.65G>C (p.Gly22Ala)	CDC73 (G22A)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2748058	NM_024529.5(CDC73):c.69_70delinsTT (p.Glu24Ter)	CDC73 (E24*)	Indel (nonsense)	Parathyroid carcinoma	GPathogenic
Select item 759441	NM_024529.5(CDC73):c.72A>G (p.Glu24=)	CDC73	Single nucleotide variant (synonymous variant)	Hyperparathyroidism 2 with jaw tumors +3 more	GConflicting classifications of pathogenicity
Select item 848837	NM_024529.5(CDC73):c.76A>G (p.Ile26Val)	CDC73 (I26V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1092731	NM_024529.5(CDC73):c.78C>T (p.Ile26=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 2166998	NM_024529.5(CDC73):c.79T>C (p.Phe27Leu)	CDC73 (F27L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1762412	NM_024529.5(CDC73):c.81C>T (p.Phe27=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 1719292	NM_024529.5(CDC73):c.83G>A (p.Gly28Glu)	CDC73 (G28E)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 531644	NM_024529.5(CDC73):c.83G>C (p.Gly28Ala)	CDC73 (G28A)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1907870	NM_024529.5(CDC73):c.84G>C (p.Gly28=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 1126537	NM_024529.5(CDC73):c.84G>A (p.Gly28=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 429954	NM_024529.5(CDC73):c.85G>T (p.Glu29Ter)	CDC73 (E29*)	Single nucleotide variant (nonsense)	Parathyroid carcinoma +1 more	GPathogenic
Select item 1462062	NM_024529.5(CDC73):c.87G>C (p.Glu29Asp)	CDC73 (E29D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1096502	NM_024529.5(CDC73):c.87G>A (p.Glu29=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 1650562	NM_024529.5(CDC73):c.90C>T (p.Phe30=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2843579	NM_024529.5(CDC73):c.92C>T (p.Ser31Phe)	CDC73 (S31F)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 569330	NM_024529.5(CDC73):c.92C>A (p.Ser31Tyr)	CDC73 (S31Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1088808	NM_024529.5(CDC73):c.93C>T (p.Ser31=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 2810313	NM_024529.5(CDC73):c.96del (p.Trp32fs)	CDC73 (W32fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 2003171	NM_024529.5(CDC73):c.99del (p.Lys34fs)	CDC73 (K34fs)	Deletion (frameshift variant)	Parathyroid carcinoma	GPathogenic
Select item 757174	NM_024529.5(CDC73):c.99C>T (p.Pro33=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma +1 more	GLikely benign
Select item 2090170	NM_024529.5(CDC73):c.100A>C (p.Lys34Gln)	CDC73 (K34Q)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2914838	NM_024529.5(CDC73):c.102G>A (p.Lys34=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2129556	NM_024529.5(CDC73):c.102G>C (p.Lys34Asn)	CDC73 (K34N)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2851102	NM_024529.5(CDC73):c.104A>G (p.Asn35Ser)	CDC73 (N35S)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1346211	NM_024529.5(CDC73):c.110A>G (p.Lys37Arg)	CDC73 (K37R)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 774030	NM_024529.5(CDC73):c.111G>A (p.Lys37=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 648670	NM_024529.5(CDC73):c.111G>C (p.Lys37Asn)	CDC73 (K37N)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 2920334	NM_024529.5(CDC73):c.114C>T (p.Thr38=)	CDC73	Single nucleotide variant (synonymous variant)	Parathyroid carcinoma	GLikely benign
Select item 1054916	NM_024529.5(CDC73):c.116A>G (p.Asn39Ser)	CDC73 (N39S)	Single nucleotide variant (missense variant)	Parathyroid carcinoma +3 more	GUncertain significance
Select item 1425100	NM_024529.5(CDC73):c.119A>G (p.Tyr40Cys)	CDC73 (Y40C)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1358121	NM_024529.5(CDC73):c.121GTT[1] (p.Val42del)	CDC73 (V42del)	Microsatellite (inframe_deletion)	Parathyroid carcinoma	GUncertain significance
Select item 2809506	NM_024529.5(CDC73):c.121G>C (p.Val41Leu)	CDC73 (V41L)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1620784	NM_024529.5(CDC73):c.126T>C (p.Val42=)	CDC73	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 3271	NM_024529.5(CDC73):c.128G>A (p.Trp43Ter)	CDC73 (W43*)	Single nucleotide variant (nonsense)	Parathyroid carcinoma	GPathogenic
Select item 2020100	NM_024529.5(CDC73):c.131G>T (p.Gly44Val)	CDC73 (G44V)	Single nucleotide variant (missense variant)	Parathyroid carcinoma	GUncertain significance
Select item 1455290	NM_024529.5(CDC73):c.131+1G>T	CDC73	Single nucleotide variant (splice donor variant)	Parathyroid carcinoma	GPathogenic
Select item 3276	NM_024529.5(CDC73):c.131+1G>A	CDC73	Single nucleotide variant (splice donor variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 241493	NM_024529.5(CDC73):c.131+4A>G	CDC73	Single nucleotide variant (intron variant)	Parathyroid carcinoma +1 more	GConflicting classifications of pathogenicity
Select item 1107816	NM_024529.5(CDC73):c.131+7C>T	CDC73	Single nucleotide variant (intron variant)	Parathyroid carcinoma	GLikely benign
Select item 758976	NM_024529.5(CDC73):c.131+7C>G	CDC73	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1148291	NM_024529.5(CDC73):c.131+8C>A	CDC73	Single nucleotide variant (intron variant)	Parathyroid carcinoma	GLikely benign

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