"Ambry Genetics"[submitter] AND "DALRD3"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3080035	NM_001009996.3(DALRD3):c.1612C>T (p.Pro538Ser)	DALRD3, WDR6 (P538S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2328760	NM_001009996.3(DALRD3):c.1586A>G (p.His529Arg)	DALRD3, WDR6 (H362R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2234459	NM_001009996.3(DALRD3):c.1549C>T (p.Arg517Cys)	DALRD3, WDR6 (P508L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2380887	NM_001009996.3(DALRD3):c.1466T>G (p.Leu489Arg)	DALRD3, WDR6 (L489R +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2376132	NM_001009996.3(DALRD3):c.1412C>T (p.Pro471Leu)	DALRD3 (P471L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509948	NM_001009996.3(DALRD3):c.1349T>C (p.Phe450Ser)	DALRD3 (F283S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494249	NM_001009996.3(DALRD3):c.1346T>G (p.Leu449Arg)	DALRD3 (L449R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333357	NM_001009996.3(DALRD3):c.1327G>A (p.Glu443Lys)	DALRD3 (E276K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329903	NM_001009996.3(DALRD3):c.1301G>A (p.Ser434Asn)	DALRD3 (S267N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221185	NM_001009996.3(DALRD3):c.1226G>A (p.Arg409His)	DALRD3 (R242H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080033	NM_001009996.3(DALRD3):c.1181C>T (p.Thr394Met)	DALRD3 (T394M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322213	NM_001009996.3(DALRD3):c.1034C>T (p.Ala345Val)	DALRD3 (A178V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327970	NM_001009996.3(DALRD3):c.1017G>T (p.Gln339His)	DALRD3 (Q172H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219688	NM_001009996.3(DALRD3):c.932A>T (p.His311Leu)	DALRD3 (H144L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532771	NM_001009996.3(DALRD3):c.887T>A (p.Leu296Gln)	DALRD3 (L129Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519965	NM_001009996.3(DALRD3):c.820A>C (p.Thr274Pro)	DALRD3 (T274P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618243	NM_001009996.3(DALRD3):c.740T>C (p.Val247Ala)	DALRD3 (V247A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301332	NM_001009996.3(DALRD3):c.667G>A (p.Glu223Lys)	DALRD3 (E223K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362329	NM_001009996.3(DALRD3):c.493G>C (p.Asp165His)	DALRD3 (D165H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322845	NM_001009996.3(DALRD3):c.487G>C (p.Val163Leu)	DALRD3 (V163L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080039	NM_001009996.3(DALRD3):c.430G>A (p.Asp144Asn)	DALRD3 (D144N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080038	NM_001009996.3(DALRD3):c.386C>T (p.Pro129Leu)	DALRD3 (P129L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523477	NM_001009996.3(DALRD3):c.386C>G (p.Pro129Arg)	DALRD3 (P129R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537046	NM_001009996.3(DALRD3):c.325G>T (p.Ala109Ser)	DALRD3 (A109S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080037	NM_001009996.3(DALRD3):c.235G>A (p.Ala79Thr)	DALRD3 (A79T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244103	NM_001009996.3(DALRD3):c.221C>T (p.Pro74Leu)	DALRD3 (P74L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080036	NM_001009996.3(DALRD3):c.200T>G (p.Leu67Arg)	DALRD3 (L67R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239516	NM_001009996.3(DALRD3):c.68G>A (p.Gly23Asp)	DALRD3 (G23D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461838	NM_001009996.3(DALRD3):c.40G>C (p.Ala14Pro)	DALRD3 (A14P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 29