RUNX1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1282402	NC_000021.9:g.34787766A>G	RUNX1	Single nucleotide variant	not provided	GBenign
Select item 417477	NC_000021.9:g.(?_34787801)_(34799462_?)del	RUNX1	Deletion	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GLikely pathogenic FDA Recognized database
Select item 339792	NM_001754.5(RUNX1):c.*4250C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339793	NM_001754.5(RUNX1):c.*4238G>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339794	NM_001754.5(RUNX1):c.*4188G>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339795	NM_001754.5(RUNX1):c.*4147C>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339796	NM_001754.5(RUNX1):c.*4140C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339797	NM_001754.5(RUNX1):c.*4032T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339798	NM_001754.5(RUNX1):c.*4003C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339799	NM_001754.5(RUNX1):c.*3977G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339800	NM_001754.5(RUNX1):c.*3944G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339801	NM_001754.5(RUNX1):c.*3721A>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 897093	NM_001754.5(RUNX1):c.*3642C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 897094	NM_001754.5(RUNX1):c.*3638G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339802	NM_001754.5(RUNX1):c.*3619A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339803	NM_001754.5(RUNX1):c.*3588G>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 897095	NM_001754.5(RUNX1):c.*3582G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339804	NM_001754.5(RUNX1):c.*3580T>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339805	NM_001754.5(RUNX1):c.*3574A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 897570	NM_001754.5(RUNX1):c.*3557C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339806	NM_001754.5(RUNX1):c.*3527T>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339807	NM_001754.5(RUNX1):c.*3444A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339808	NM_001754.5(RUNX1):c.*3417A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339809	NM_001754.5(RUNX1):c.*3380A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339810	NM_001754.5(RUNX1):c.*3345A>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339811	NM_001754.5(RUNX1):c.*3297T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 898727	NM_001754.5(RUNX1):c.*3281G>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339812	NM_001754.5(RUNX1):c.*3277G>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339813	NM_001754.5(RUNX1):c.*3229C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339814	NM_001754.5(RUNX1):c.*3138C>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 898728	NM_001754.5(RUNX1):c.*3090A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339815	NM_001754.5(RUNX1):c.*3060T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 898729	NM_001754.5(RUNX1):c.*3028T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339816	NM_001754.5(RUNX1):c.*3021A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 895756	NM_001754.5(RUNX1):c.*2912A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339817	NM_001754.5(RUNX1):c.*2886T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339818	NM_001754.5(RUNX1):c.*2840A>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339819	NM_001754.5(RUNX1):c.*2822C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339820	NM_001754.5(RUNX1):c.*2780A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339821	NM_001754.5(RUNX1):c.*2770C>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339822	NM_001754.5(RUNX1):c.*2768A>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339823	NM_001754.5(RUNX1):c.*2678A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339824	NM_001754.5(RUNX1):c.*2642A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339825	NM_001754.5(RUNX1):c.*2626A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339826	NM_001754.5(RUNX1):c.2594_2597del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339827	NM_001754.5(RUNX1):c.*2533TG[10]	RUNX1	Microsatellite (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339828	NM_001754.5(RUNX1):c.*2532G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 896040	NM_001754.5(RUNX1):c.*2531C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339829	NM_001754.5(RUNX1):c.*2517TG[8]	RUNX1	Microsatellite (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339830	NM_001754.5(RUNX1):c.*2474T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GBenign FDA Recognized database
Select item 339831	NM_001754.5(RUNX1):c.*2467dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 896041	NM_001754.5(RUNX1):c.*2376G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339832	NM_001754.5(RUNX1):c.*2366G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 896042	NM_001754.5(RUNX1):c.*2347C>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339833	NM_001754.5(RUNX1):c.*2329A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339834	NM_001754.5(RUNX1):c.*2320T>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339835	NM_001754.5(RUNX1):c.*2285A>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339836	NM_001754.5(RUNX1):c.*2217dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339837	NM_001754.5(RUNX1):c.*2201dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 897627	NM_001754.5(RUNX1):c.*2201T>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339838	NM_001754.5(RUNX1):c.*2193del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339839	NM_001754.5(RUNX1):c.*2005A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 897628	NM_001754.5(RUNX1):c.*1967G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339840	NM_001754.5(RUNX1):c.*1938C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339841	NM_001754.5(RUNX1):c.*1823A>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 898790	NM_001754.5(RUNX1):c.*1788A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339842	NM_001754.5(RUNX1):c.*1720C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339843	NM_001754.5(RUNX1):c.1683_1684del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339844	NM_001754.5(RUNX1):c.*1466G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339845	NM_001754.5(RUNX1):c.*1455A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 339846	NM_001754.5(RUNX1):c.*1430C>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 898791	NM_001754.5(RUNX1):c.*1400G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 898792	NM_001754.5(RUNX1):c.*1360C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339847	NM_001754.5(RUNX1):c.*1295G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 895824	NM_001754.5(RUNX1):c.*1293A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339848	NM_001754.5(RUNX1):c.*1213C>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GUncertain significance FDA Recognized database
Select item 895825	NM_001754.5(RUNX1):c.*1158C>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GLikely benign FDA Recognized database
Select item 339849	NM_001754.5(RUNX1):c.*1138C>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339850	NM_001754.5(RUNX1):c.*1096A>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 895826	NM_001754.5(RUNX1):c.*1078A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339851	NM_001754.5(RUNX1):c.*1012C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 895827	NM_001754.5(RUNX1):c.*940G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339852	NM_001754.5(RUNX1):c.*933T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339853	NM_001754.5(RUNX1):c.*919A>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339854	NM_001754.5(RUNX1):c.*917del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 896106	NM_001754.5(RUNX1):c.*821G>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 896107	NM_001754.5(RUNX1):c.*801A>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339855	NM_001754.5(RUNX1):c.*730dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339856	NM_001754.5(RUNX1):c.*700dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339858	NM_001754.5(RUNX1):c.*682dup	RUNX1	Duplication (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 +1 more	GUncertain significance
Select item 339857	NM_001754.5(RUNX1):c.*683G>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339859	NM_001754.5(RUNX1):c.*667del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339860	NM_001754.5(RUNX1):c.*613A>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339861	NM_001754.5(RUNX1):c.*587T>A	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 339862	NM_001754.5(RUNX1):c.*582del	RUNX1	Deletion (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 896108	NM_001754.5(RUNX1):c.*569T>G	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339863	NM_001754.5(RUNX1):c.*559T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 339864	NM_001754.5(RUNX1):c.*484T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematologic cancer predisposition syndrome	GBenign FDA Recognized database
Select item 897695	NM_001754.5(RUNX1):c.*467T>C	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance
Select item 897696	NM_001754.5(RUNX1):c.*463C>T	RUNX1	Single nucleotide variant (3 prime UTR variant)	Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1	GUncertain significance

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