ClinVar for Gene (Select 5890) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151066	NM_133510.4(RAD51B):c.964A>T (p.Ile322Phe)	RAD51B (I322F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151065	NM_133510.4(RAD51B):c.692G>A (p.Arg231Lys)	RAD51B (R193K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151064	NM_133510.4(RAD51B):c.295G>A (p.Ala99Thr)	RAD51B (A61T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151063	NM_133510.4(RAD51B):c.134G>A (p.Ser45Asn)	RAD51B (S45N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151062	NM_133510.4(RAD51B):c.115A>G (p.Met39Val)	RAD51B (M39V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3057100	NM_133510.4(RAD51B):c.316-7_316-3del	RAD51B	Deletion (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3056969	NM_133510.4(RAD51B):c.316-14_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3056035	NM_133510.4(RAD51B):c.316-17_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3055947	NM_133510.4(RAD51B):c.316-18_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3054260	NM_133510.4(RAD51B):c.316-19_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3050947	NM_001321815.1(RAD51B):c.961A>T (p.Lys321Ter)	RAD51B (K321*)	Single nucleotide variant (3 prime UTR variant +3 more)	RAD51B-related disorder	GLikely benign
Select item 3048756	NM_133510.4(RAD51B):c.316-13_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3046979	NM_001321818.2(RAD51B):c.1041G>T (p.Gln347His)	RAD51B (Q347H)	Single nucleotide variant (missense variant)	RAD51B-related disorder	GLikely benign
Select item 3044143	NM_133510.4(RAD51B):c.316-27_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3044129	NM_133509.5(RAD51B):c.1037-54294dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3040588	NM_133510.4(RAD51B):c.316-16_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3038600	NM_133510.4(RAD51B):c.316-6_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3038249	NM_133510.4(RAD51B):c.316-8_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3037983	NM_133510.4(RAD51B):c.316-15_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3037700	NM_001321821.2(RAD51B):c.1125T>C (p.Asp375=)	RAD51B	Single nucleotide variant (3 prime UTR variant +2 more)	RAD51B-related disorder	GBenign
Select item 3037667	NM_133510.4(RAD51B):c.316-11_316-3del	RAD51B	Deletion (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3034556	NM_133510.4(RAD51B):c.1037-8T>C	RAD51B	Single nucleotide variant (intron variant)	RAD51B-related disorder	GBenign
Select item 3033284	NM_133510.4(RAD51B):c.316-12_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder	GLikely benign
Select item 3031670	NM_133510.4(RAD51B):c.541C>T (p.Arg181Trp)	RAD51B (R143W +2 more)	Single nucleotide variant (missense variant)	RAD51B-related disorder	GLikely benign
Select item 3026354	NM_133510.4(RAD51B):c.316-12_316-3del	RAD51B	Deletion (intron variant)	not provided	GLikely benign
Select item 2684729	GRCh37/hg19 14q23.3-24.1(chr14:67443098-68423187)x3	ARG2, ATP6V1D +13 more	Copy number gain	not provided	GUncertain significance
Select item 2684728	GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	ACOT4, ACOT6 +353 more	Copy number gain	not provided	GPathogenic
Select item 2684726	GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3	ACTR10, AKAP5 +71 more	Copy number gain	not provided	GLikely pathogenic
Select item 2644342	NM_133510.4(RAD51B):c.316-16_316-3dup	RAD51B	Duplication (intron variant)	not provided	GLikely benign
Select item 2644341	NM_133510.4(RAD51B):c.316-10_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder +1 more	GBenign/Likely benign
Select item 2644340	NM_133510.4(RAD51B):c.316-9_316-3dup	RAD51B	Duplication (intron variant)	RAD51B-related disorder +1 more	GBenign/Likely benign
Select item 2622538	NM_133510.4(RAD51B):c.358A>G (p.Met120Val)	RAD51B (M120V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2577876	NM_001321818.2(RAD51B):c.1037-71695GT[3]	RAD51B	Microsatellite (3 prime UTR variant +3 more)	Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	GUncertain significance
Select item 2490808	NM_133510.4(RAD51B):c.919C>G (p.Arg307Gly)	RAD51B (R307G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2423522	NC_000014.8:g.(?_68699594)_(70654407_?)del	GALNT16, ZFP36L1 +13 more	Deletion	not provided	GPathogenic
Select item 2400760	NM_133510.4(RAD51B):c.868A>G (p.Ser290Gly)	RAD51B (S171G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389640	NM_133510.4(RAD51B):c.727A>G (p.Lys243Glu)	RAD51B (K205E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379095	NM_133510.4(RAD51B):c.879A>G (p.Ile293Met)	RAD51B (I174M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300493	NM_133510.4(RAD51B):c.877A>G (p.Ile293Val)	RAD51B (I293V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241565	NM_133510.4(RAD51B):c.529G>C (p.Val177Leu)	RAD51B (V177L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237550	NM_133510.4(RAD51B):c.796G>A (p.Ala266Thr)	RAD51B (A228T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220949	NM_133510.4(RAD51B):c.361A>T (p.Met121Leu)	RAD51B (M121L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203761	NM_133510.4(RAD51B):c.957G>A (p.Gln319=)	RAD51B	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 1707441	GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	ABCD4, ABHD12B +447 more	Copy number gain	See cases	GPathogenic
Select item 1678964	NM_001321818.2(RAD51B):c.1037-88272G>T	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678963	NM_001321818.2(RAD51B):c.1037-88275_1037-88274dup	RAD51B	Duplication (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678962	NM_001321818.2(RAD51B):c.1037-88322G>T	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678961	NM_001321818.2(RAD51B):c.1037-88328T>G	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 1678960	NM_001321818.2(RAD51B):c.1037-88357C>T	RAD51B (H378Y)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 1678959	NM_001321818.2(RAD51B):c.1036+28946C>T	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678958	NM_001321818.2(RAD51B):c.1036+28871C>T	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678957	NM_133510.4(RAD51B):c.1037-16T>C	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678956	NM_133510.4(RAD51B):c.914A>T (p.Asn305Ile)	RAD51B (N186I +2 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 1678955	NM_133510.4(RAD51B):c.843C>T (p.Ser281=)	RAD51B	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678954	NM_133510.4(RAD51B):c.756+18T>C	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678953	NM_133510.4(RAD51B):c.748T>G (p.Ser250Ala)	RAD51B (S131A +2 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GBenign
Select item 1678952	NM_133510.4(RAD51B):c.728A>G (p.Lys243Arg)	RAD51B (K124R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1678951	NM_133510.4(RAD51B):c.699G>A (p.Lys233=)	RAD51B	Single nucleotide variant (synonymous variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678950	NM_133510.4(RAD51B):c.523A>C (p.Ser175Arg)	RAD51B (S137R +2 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GBenign
Select item 1678949	NM_133510.4(RAD51B):c.476G>A (p.Arg159His)	RAD51B (R121H +2 more)	Single nucleotide variant (missense variant)	RAD51B-related disorder +1 more	GLikely benign
Select item 1678948	NM_133510.4(RAD51B):c.453-10del	RAD51B	Deletion (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678947	NM_133510.4(RAD51B):c.453-32_453-31del	RAD51B	Deletion (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678946	NM_133510.4(RAD51B):c.452+32T>C	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome	GLikely benign
Select item 1678945	NM_133510.4(RAD51B):c.436G>A (p.Ala146Thr)	RAD51B (A108T +2 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 1676677	NM_133510.4(RAD51B):c.452+2T>C	RAD51B	Single nucleotide variant (splice donor variant)	not provided	Gnot provided
Select item 1527824	GRCh37/hg19 14q24.1(chr14:68448694-68854357)	RAD51B	Copy number gain	not specified	GUncertain significance
Select item 1340745	GRCh37/hg19 14q24.1(chr14:68341429-68567227)x1	RAD51B	Copy number loss	not provided	GUncertain significance
Select item 1296249	NM_133510.4(RAD51B):c.315+214A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1292857	NM_133510.4(RAD51B):c.84+25T>C	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291091	NM_133510.4(RAD51B):c.1036+145G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290117	NM_133510.4(RAD51B):c.*242G>A	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1289591	NM_133509.5(RAD51B):c.1036+44829G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283496	NM_133510.4(RAD51B):c.453-263A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281658	NM_133510.4(RAD51B):c.957+338A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271766	NM_133510.4(RAD51B):c.84+120G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271467	NM_133510.4(RAD51B):c.757-83T>C	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270868	NM_133510.4(RAD51B):c.199-22dup	RAD51B	Duplication (intron variant)	not provided	GBenign
Select item 1270763	NM_133510.4(RAD51B):c.85-274G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270487	NM_133510.4(RAD51B):c.84+82T>C	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269958	NM_133510.4(RAD51B):c.*83G>A	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1264893	NM_133510.4(RAD51B):c.84+28T>G	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1264669	NM_133510.4(RAD51B):c.515T>G (p.Leu172Trp)	RAD51B (L134W +2 more)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1264510	NM_133510.4(RAD51B):c.316-45A>T	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1259949	NM_133510.4(RAD51B):c.84+176T>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258325	NM_133510.4(RAD51B):c.453-26G>A	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1248963	NM_133510.4(RAD51B):c.854-103A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248492	NM_133510.4(RAD51B):c.199-33G>T	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1247355	NM_002877.6(RAD51B):c.1037-95C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245734	NM_133510.4(RAD51B):c.1037-292A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244539	NM_133510.4(RAD51B):c.1037-218T>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243789	NM_133509.5(RAD51B):c.1036+44962A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243637	NM_133510.4(RAD51B):c.757-26T>C	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1243504	NM_133510.4(RAD51B):c.756+231C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241451	NM_133509.5(RAD51B):c.1036+44868T>C	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241170	NM_133510.4(RAD51B):c.85-218T>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240432	NM_133510.4(RAD51B):c.1037-33del	RAD51B	Deletion (intron variant)	not provided	GBenign
Select item 1238204	NM_133510.4(RAD51B):c.85-283C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231988	NM_133510.4(RAD51B):c.199-21C>T	RAD51B	Single nucleotide variant (intron variant)	Hereditary breast ovarian cancer syndrome +1 more	GBenign
Select item 1231625	NM_133510.4(RAD51B):c.757-98420A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230269	NM_133510.4(RAD51B):c.572+200G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign

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