"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAD21"[ge - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3047087	NM_006265.3(RAD21):c.1836A>C (p.Thr612=)	RAD21	Single nucleotide variant (synonymous variant)	RAD21-related disorder	GLikely benign
Select item 2631162	NM_006265.3(RAD21):c.1627G>A (p.Asp543Asn)	RAD21 (D543N)	Single nucleotide variant (missense variant)	RAD21-related disorder	GUncertain significance
Select item 473191	NM_006265.3(RAD21):c.1515C>G (p.Pro505=)	RAD21	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 588094	NM_006265.3(RAD21):c.1503T>G (p.Pro501=)	RAD21	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 159805	NM_006265.3(RAD21):c.1440T>C (p.Ala480=)	RAD21	Single nucleotide variant (synonymous variant)	Mungan syndrome +3 more	GBenign
Select item 3031507	NM_006265.3(RAD21):c.1421A>G (p.Gln474Arg)	RAD21 (Q474R)	Single nucleotide variant (missense variant)	RAD21-related disorder	GUncertain significance
Select item 259961	NM_006265.3(RAD21):c.1185G>A (p.Pro395=)	RAD21	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign
Select item 3041081	NM_006265.3(RAD21):c.1161+5T>C	RAD21	Single nucleotide variant (intron variant)	RAD21-related disorder	GLikely benign
Select item 3054602	NM_006265.3(RAD21):c.1134G>A (p.Gln378=)	RAD21	Single nucleotide variant (synonymous variant)	RAD21-related disorder	GLikely benign
Select item 3061503	NM_006265.3(RAD21):c.1131T>C (p.Ala377=)	RAD21	Single nucleotide variant (synonymous variant)	RAD21-related disorder	GLikely benign
Select item 3032232	NM_006265.3(RAD21):c.937+1G>A	RAD21	Single nucleotide variant (splice donor variant)	RAD21-related disorder	GLikely pathogenic
Select item 1761829	NM_006265.3(RAD21):c.805A>G (p.Asn269Asp)	RAD21 (N269D)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 473194	NM_006265.3(RAD21):c.786C>T (p.Asp262=)	RAD21	Single nucleotide variant (synonymous variant)	RAD21-related disorder +3 more	GBenign/Likely benign
Select item 159808	NM_006265.3(RAD21):c.688+8G>A	RAD21	Single nucleotide variant (intron variant)	Mungan syndrome +2 more	GBenign
Select item 715157	NM_006265.3(RAD21):c.645T>C (p.Tyr215=)	RAD21	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 2631514	NM_006265.3(RAD21):c.386T>C (p.Val129Ala)	RAD21 (V129A)	Single nucleotide variant (missense variant)	RAD21-related disorder	GUncertain significance
Select item 2631614	NM_006265.3(RAD21):c.160C>T (p.Arg54Trp)	RAD21 (R54W)	Single nucleotide variant (missense variant)	RAD21-related disorder	GLikely pathogenic
Select item 772049	NM_006265.3(RAD21):c.159A>G (p.Leu53=)	RAD21	Single nucleotide variant (synonymous variant)	RAD21-related disorder +1 more	GLikely benign