ADRA2A[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 511078	NM_000681.3(ADRA2A):c.-1252G>C	ADRA2A	Single nucleotide variant	not specified	GLikely benign
Select item 1316601	NC_000010.11:g.111076814A>G	ADRA2A	Single nucleotide variant	not provided	GLikely benign
Select item 2268460	NM_000681.4(ADRA2A):c.5T>A (p.Phe2Tyr)	ADRA2A (F2Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621257	NM_000681.4(ADRA2A):c.37T>C (p.Phe13Leu)	ADRA2A (F13L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542401	NM_000681.4(ADRA2A):c.103G>A (p.Gly35Arg)	ADRA2A (G35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337117	NM_000681.4(ADRA2A):c.104G>A (p.Gly35Glu)	ADRA2A (G35E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 788598	NM_000681.4(ADRA2A):c.225G>C (p.Thr75=)	ADRA2A	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2608392	NM_000681.4(ADRA2A):c.253C>T (p.Leu85Phe)	ADRA2A (L85F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3036098	NM_000681.4(ADRA2A):c.298C>T (p.Leu100Phe)	ADRA2A (L100F)	Single nucleotide variant (missense variant)	ADRA2A-related disorder	GUncertain significance
Select item 3273856	NM_000681.4(ADRA2A):c.352A>G (p.Lys118Glu)	ADRA2A (K118E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546463	NM_000681.4(ADRA2A):c.367A>C (p.Ile123Leu)	ADRA2A (I123L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713348	NM_000681.4(ADRA2A):c.381C>G (p.Leu127=)	ADRA2A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2539542	NM_000681.4(ADRA2A):c.407T>C (p.Ile136Thr)	ADRA2A (I136T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1336507	NM_000681.4(ADRA2A):c.463G>A (p.Glu155Lys)	ADRA2A (E155K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3090802	NM_000681.4(ADRA2A):c.530C>T (p.Ala177Val)	ADRA2A (A177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304090	NM_000681.4(ADRA2A):c.583G>A (p.Gly195Ser)	ADRA2A (G195S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3347064	NM_000681.4(ADRA2A):c.642G>T (p.Ser214=)	ADRA2A	Single nucleotide variant (synonymous variant)	ADRA2A-related disorder	GLikely benign
Select item 2404360	NM_000681.4(ADRA2A):c.682A>G (p.Ile228Val)	ADRA2A (I228V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278128	NM_000681.4(ADRA2A):c.700A>G (p.Ile234Val)	ADRA2A (I234V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090807	NM_000681.4(ADRA2A):c.736C>G (p.Pro246Ala)	ADRA2A (P246A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2636029	NM_000681.4(ADRA2A):c.796A>G (p.Asn266Asp)	ADRA2A (N266D)	Single nucleotide variant (missense variant)	ADRA2A-related disorder	GUncertain significance
Select item 1338705	NM_000681.4(ADRA2A):c.810_827del (p.Glu271_Pro276del)	ADRA2A	Deletion (inframe_deletion)	not specified	GLikely benign
Select item 3090809	NM_000681.4(ADRA2A):c.806G>A (p.Gly269Asp)	ADRA2A (G269D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273852	NM_000681.4(ADRA2A):c.815G>T (p.Arg272Leu)	ADRA2A (R272L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3357660	NM_000681.4(ADRA2A):c.840G>A (p.Glu280=)	ADRA2A	Single nucleotide variant (synonymous variant)	ADRA2A-related disorder	GLikely benign
Select item 3090811	NM_000681.4(ADRA2A):c.866A>G (p.Asn289Ser)	ADRA2A (N289S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281758	NM_000681.4(ADRA2A):c.871G>A (p.Ala291Thr)	ADRA2A (A291T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 779122	NM_000681.4(ADRA2A):c.894C>G (p.Ala298=)	ADRA2A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2391901	NM_000681.4(ADRA2A):c.895G>A (p.Gly299Arg)	ADRA2A (G299R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387356	NM_000681.4(ADRA2A):c.902G>A (p.Arg301His)	ADRA2A (R301H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218474	NM_000681.4(ADRA2A):c.991C>G (p.Arg331Gly)	ADRA2A (R331G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273860	NM_000681.4(ADRA2A):c.1030G>A (p.Gly344Ser)	ADRA2A (G344S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090778	NM_000681.4(ADRA2A):c.1061C>A (p.Ala354Glu)	ADRA2A (A354E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2457726	NM_000681.4(ADRA2A):c.1064C>T (p.Thr355Met)	ADRA2A (T355M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617755	NM_000681.4(ADRA2A):c.1072G>A (p.Gly358Arg)	ADRA2A (G358R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3090789	NM_000681.4(ADRA2A):c.1073G>A (p.Gly358Glu)	ADRA2A (G358E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273851	NM_000681.4(ADRA2A):c.1090C>T (p.Pro364Ser)	ADRA2A (P364S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516764	NM_000681.4(ADRA2A):c.1373G>A (p.Arg458Gln)	ADRA2A (R458Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234569	NM_000681.4(ADRA2A):c.1376G>A (p.Gly459Glu)	ADRA2A (G459E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2691730	NM_000681.4(ADRA2A):c.*427A>G	ADRA2A	Single nucleotide variant (3 prime UTR variant)	Lipodystrophy, familial partial, type 8	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 40