DHX15[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2227187	NM_001358.3(DHX15):c.2350A>G (p.Ile784Val)	DHX15 (I784V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082146	NM_001358.3(DHX15):c.2330A>G (p.Lys777Arg)	DHX15 (K777R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271846	NM_001358.3(DHX15):c.2042C>T (p.Thr681Ile)	DHX15 (T681I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082145	NM_001358.3(DHX15):c.1975A>G (p.Asn659Asp)	DHX15 (N659D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082144	NM_001358.3(DHX15):c.1724T>C (p.Val575Ala)	DHX15 (V575A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570674	NM_001358.3(DHX15):c.1327A>G (p.Lys443Glu)	DHX15 (K443E)	Single nucleotide variant (missense variant)	Seizure +7 more	GUncertain significance
Select item 2533884	NM_001358.3(DHX15):c.1195C>T (p.Arg399Cys)	DHX15 (R399C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 932460	NM_001358.3(DHX15):c.999A>G (p.Glu333=)	DHX15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2478193	NM_001358.3(DHX15):c.727C>T (p.Arg243Cys)	DHX15 (R243C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307975	NM_001358.3(DHX15):c.550C>G (p.Pro184Ala)	DHX15 (P184A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2654696	NM_001358.3(DHX15):c.354C>T (p.Phe118=)	DHX15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2524899	NM_001358.3(DHX15):c.326C>T (p.Thr109Met)	DHX15 (T109M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321639	NM_001358.3(DHX15):c.314A>G (p.His105Arg)	DHX15 (H105R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537601	NM_001358.3(DHX15):c.304C>T (p.His102Tyr)	DHX15 (H102Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509325	NM_001358.3(DHX15):c.302C>T (p.Thr101Met)	DHX15 (T101M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518999	NM_001358.3(DHX15):c.286C>T (p.His96Tyr)	DHX15 (H96Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271844	NM_001358.3(DHX15):c.275C>T (p.Thr92Met)	DHX15 (T92M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271845	NM_001358.3(DHX15):c.131G>A (p.Arg44His)	DHX15 (R44H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518723	NM_001358.3(DHX15):c.125G>A (p.Arg42Gln)	DHX15 (R42Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226097	NM_001358.3(DHX15):c.65C>T (p.Thr22Ile)	DHX15 (T22I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20