ADRA1D[gene] and "single gene"[properties] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545548	NM_000678.4(ADRA1D):c.1707G>C (p.Glu569Asp)	ADRA1D (E569D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090698	NM_000678.4(ADRA1D):c.1541T>C (p.Val514Ala)	ADRA1D (V514A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314192	NM_000678.4(ADRA1D):c.1537A>G (p.Lys513Glu)	ADRA1D (K513E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610132	NM_000678.4(ADRA1D):c.1507T>C (p.Phe503Leu)	ADRA1D (F503L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2312941	NM_000678.4(ADRA1D):c.1432C>A (p.Pro478Thr)	ADRA1D (P478T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255115	NM_000678.4(ADRA1D):c.1430C>G (p.Thr477Arg)	ADRA1D (T477R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304179	NM_000678.4(ADRA1D):c.1427G>T (p.Gly476Val)	ADRA1D (G476V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288067	NM_000678.4(ADRA1D):c.1370C>T (p.Pro457Leu)	ADRA1D (P457L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516871	NM_000678.4(ADRA1D):c.1309C>A (p.His437Asn)	ADRA1D (H437N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262493	NM_000678.4(ADRA1D):c.1231C>G (p.Arg411Gly)	ADRA1D (R411G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529178	NM_000678.4(ADRA1D):c.1219C>A (p.Arg407Ser)	ADRA1D (R407S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555114	NM_000678.4(ADRA1D):c.1201A>G (p.Ile401Val)	ADRA1D (I401V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365798	NM_000678.4(ADRA1D):c.957C>G (p.His319Gln)	ADRA1D (H319Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212155	NM_000678.4(ADRA1D):c.950G>A (p.Gly317Glu)	ADRA1D (G317E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301528	NM_000678.4(ADRA1D):c.938C>A (p.Thr313Lys)	ADRA1D (T313K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090761	NM_000678.4(ADRA1D):c.926G>C (p.Arg309Pro)	ADRA1D (R309P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348740	NM_000678.4(ADRA1D):c.844C>G (p.Arg282Gly)	ADRA1D (R282G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305244	NM_000678.4(ADRA1D):c.818T>C (p.Met273Thr)	ADRA1D (M273T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376745	NM_000678.4(ADRA1D):c.778G>A (p.Val260Met)	ADRA1D (V260M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299527	NM_000678.4(ADRA1D):c.763G>C (p.Ala255Pro)	ADRA1D (A255P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519990	NM_000678.4(ADRA1D):c.739G>A (p.Gly247Ser)	ADRA1D (G247S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350021	NM_000678.4(ADRA1D):c.722C>T (p.Pro241Leu)	ADRA1D (P241L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090731	NM_000678.4(ADRA1D):c.721C>A (p.Pro241Thr)	ADRA1D (P241T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 762311	NM_000678.4(ADRA1D):c.684C>G (p.Ser228=)	ADRA1D	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2532201	NM_000678.4(ADRA1D):c.628G>C (p.Glu210Gln)	ADRA1D (E210Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479087	NM_000678.4(ADRA1D):c.568A>C (p.Ile190Leu)	ADRA1D (I190L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326591	NM_000678.4(ADRA1D):c.568A>T (p.Ile190Phe)	ADRA1D (I190F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492280	NM_000678.4(ADRA1D):c.496C>T (p.Arg166Cys)	ADRA1D (R166C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522594	NM_000678.4(ADRA1D):c.458C>T (p.Ser153Leu)	ADRA1D (S153L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334323	NM_000678.4(ADRA1D):c.370A>C (p.Asn124His)	ADRA1D (N124H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382865	NM_000678.4(ADRA1D):c.331G>A (p.Val111Met)	ADRA1D (V111M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090703	NM_000678.4(ADRA1D):c.217G>A (p.Gly73Arg)	ADRA1D (G73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090701	NM_000678.4(ADRA1D):c.201C>A (p.Ser67Arg)	ADRA1D (S67R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207251	NM_000678.4(ADRA1D):c.173G>A (p.Gly58Asp)	ADRA1D (G58D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562243	NM_000678.4(ADRA1D):c.157G>A (p.Gly53Ser)	ADRA1D (G53S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324797	NM_000678.4(ADRA1D):c.107C>G (p.Ala36Gly)	ADRA1D (A36G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090670	NM_000678.4(ADRA1D):c.104C>G (p.Ala35Gly)	ADRA1D (A35G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472280	NM_000678.4(ADRA1D):c.89G>T (p.Gly30Val)	ADRA1D (G30V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090729	NM_000678.4(ADRA1D):c.65G>A (p.Gly22Asp)	ADRA1D (G22D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460410	NM_000678.4(ADRA1D):c.59C>G (p.Ala20Gly)	ADRA1D (A20G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460409	NM_000678.4(ADRA1D):c.58G>A (p.Ala20Thr)	ADRA1D (A20T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 41