"GeneDx"[submitter] AND "RAD51B"[gene] - ClinVar

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Search results

Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1292857	NM_133510.4(RAD51B):c.84+25T>C	RAD51B	Single nucleotide variant (intron variant)	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 1270487	NM_133510.4(RAD51B):c.84+82T>C	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 1259949	NM_133510.4(RAD51B):c.84+176T>G	RAD51B	Single nucleotide variant (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 1270763	NM_133510.4(RAD51B):c.85-274G>A	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 1248492	NM_133510.4(RAD51B):c.199-33G>T	RAD51B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1270868	NM_133510.4(RAD51B):c.199-22dup	RAD51B	Duplication (intron variant)	not provided	GBenign
Select item 1231988	NM_133510.4(RAD51B):c.199-21C>T	RAD51B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1296249	NM_133510.4(RAD51B):c.315+214A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183458	NM_133510.4(RAD51B):c.316-283G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	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 1229156	NM_133510.4(RAD51B):c.452+246C>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 1258325	NM_133510.4(RAD51B):c.453-26G>A	RAD51B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1264669	NM_133510.4(RAD51B):c.515T>G (p.Leu172Trp)	RAD51B (L134W +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 710709	NM_133510.4(RAD51B):c.539A>G (p.Tyr180Cys)	RAD51B (Y61C +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1230269	NM_133510.4(RAD51B):c.572+200G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243504	NM_133510.4(RAD51B):c.756+231C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231625	NM_133510.4(RAD51B):c.757-98420A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 225821	NM_133510.4(RAD51B):c.757-98173T>C	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 1228217	NM_133510.4(RAD51B):c.757-49T>C	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 1248963	NM_133510.4(RAD51B):c.854-103A>G	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183734	NM_133510.4(RAD51B):c.957+125C>A	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 1181212	NM_133510.4(RAD51B):c.958-199A>G	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 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 1183158	NM_133510.4(RAD51B):c.1037-120T>C	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 1269958	NM_133510.4(RAD51B):c.*83G>A	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	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 1247355	NM_002877.6(RAD51B):c.1037-95C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226376	NM_133509.5(RAD51B):c.1036+44587A>C	RAD51B	Single nucleotide variant (intron variant)	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 1241451	NM_133509.5(RAD51B):c.1036+44868T>C	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 225822	NM_133509.5(RAD51B):c.1037-26520C>T	RAD51B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 523174	NM_133509.5(RAD51B):c.1094C>G (p.Pro365Arg)	RAD51B (P365R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1226381	NM_001321809.2(RAD51B):c.1037-7731C>T	RAD51B	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

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Items: 45