ADRA1A[gene] and "single gene"[properties] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2309295	NM_000680.4(ADRA1A):c.1387G>A (p.Gly463Arg)	ADRA1A (G463R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090484	NM_000680.4(ADRA1A):c.1321C>G (p.Pro441Ala)	ADRA1A (P441A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3273688	NM_000680.4(ADRA1A):c.1315T>C (p.Ser439Pro)	ADRA1A (S439P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090481	NM_000680.4(ADRA1A):c.1268G>A (p.Arg423Gln)	ADRA1A (R423Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090479	NM_000680.4(ADRA1A):c.1235T>C (p.Val412Ala)	ADRA1A (V412A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 721114	NM_000680.4(ADRA1A):c.1203T>G (p.Ser401=)	ADRA1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2545872	NM_000680.4(ADRA1A):c.1088C>G (p.Pro363Arg)	ADRA1A (P363R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517772	NM_000680.4(ADRA1A):c.1040G>A (p.Cys347Tyr)	ADRA1A (C347Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090468	NM_000680.4(ADRA1A):c.1031A>C (p.Gln344Pro)	ADRA1A (Q344P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3273699	NM_000680.4(ADRA1A):c.915A>C (p.Glu305Asp)	ADRA1A (E305D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373253	NM_000680.4(ADRA1A):c.877C>T (p.Pro293Ser)	ADRA1A (P293S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544369	NM_000680.4(ADRA1A):c.869T>C (p.Leu290Ser)	ADRA1A (L290S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 782112	NM_000680.4(ADRA1A):c.819G>T (p.Thr273=)	ADRA1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2390617	NM_000680.4(ADRA1A):c.743T>C (p.Met248Thr)	ADRA1A (M248T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459897	NM_000680.4(ADRA1A):c.737G>A (p.Ser246Asn)	ADRA1A (S246N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 729684	NM_000680.4(ADRA1A):c.723C>A (p.Ala241=)	ADRA1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2319444	NM_000680.4(ADRA1A):c.673G>C (p.Asp225His)	ADRA1A (D225H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090542	NM_000680.4(ADRA1A):c.661G>A (p.Gly221Ser)	ADRA1A (G221S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090537	NM_000680.4(ADRA1A):c.646C>G (p.Arg216Gly)	ADRA1A (R216G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515124	NM_000680.4(ADRA1A):c.566C>A (p.Ala189Glu)	ADRA1A (A189E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476111	NM_000680.4(ADRA1A):c.475A>G (p.Ile159Val)	ADRA1A (I159V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 775260	NM_000680.4(ADRA1A):c.462C>G (p.Ser154=)	ADRA1A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2313357	NM_000680.4(ADRA1A):c.461C>T (p.Ser154Phe)	ADRA1A (S154F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 778029	NM_000680.4(ADRA1A):c.460T>G (p.Ser154Ala)	ADRA1A (S154A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3090520	NM_000680.4(ADRA1A):c.452G>C (p.Trp151Ser)	ADRA1A (W151S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568452	NM_000680.4(ADRA1A):c.404C>T (p.Pro135Leu)	ADRA1A (P135L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3273706	NM_000680.4(ADRA1A):c.378C>G (p.Ile126Met)	ADRA1A (I126M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090515	NM_000680.4(ADRA1A):c.376A>C (p.Ile126Leu)	ADRA1A (I126L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090512	NM_000680.4(ADRA1A):c.289G>T (p.Val97Phe)	ADRA1A (V97F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3090501	NM_000680.4(ADRA1A):c.227C>T (p.Thr76Ile)	ADRA1A (T76I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507607	NM_000680.4(ADRA1A):c.212C>A (p.Ala71Asp)	ADRA1A (A71D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479570	NM_000680.4(ADRA1A):c.175T>C (p.Ser59Pro)	ADRA1A (S59P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479569	NM_000680.4(ADRA1A):c.173A>C (p.His58Pro)	ADRA1A (H58P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226166	NM_000680.4(ADRA1A):c.155C>T (p.Ala52Val)	ADRA1A (A52V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463887	NM_000680.4(ADRA1A):c.142A>G (p.Ile48Val)	ADRA1A (I48V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267668	NM_000680.4(ADRA1A):c.22G>T (p.Ala8Ser)	ADRA1A (A8S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 815115	GRCh37/hg19 8p21.2(chr8:26594052-26663554)x1	ADRA1A	Copy number loss	not provided	GUncertain significance

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Items: 37