ADRB3[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1264874	NM_000025.3(ADRB3):c.*250G>C	ADRB3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1244998	NM_000025.3(ADRB3):c.1206-96A>G	ADRB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288105	NM_000025.3(ADRB3):c.1205+307dup	ADRB3	Duplication (intron variant)	not provided	GBenign
Select item 1230608	NM_000025.3(ADRB3):c.1205+14G>T	ADRB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3091025	NM_000025.3(ADRB3):c.1120G>A (p.Ala374Thr)	ADRB3 (A374T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206328	NM_000025.3(ADRB3):c.1120G>T (p.Ala374Ser)	ADRB3 (A374S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 707946	NM_000025.3(ADRB3):c.1057C>T (p.Arg353Cys)	ADRB3 (R353C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3091021	NM_000025.3(ADRB3):c.1027C>G (p.Pro343Ala)	ADRB3 (P343A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1050424	NM_000025.3(ADRB3):c.1013A>G (p.Asn338Ser)	ADRB3 (N338S)	Single nucleotide variant (missense variant)	Obesity +1 more	GUncertain significance
Select item 3091098	NM_000025.3(ADRB3):c.985C>T (p.Leu329Phe)	ADRB3 (L329F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 748895	NM_000025.3(ADRB3):c.978G>T (p.Pro326=)	ADRB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2560782	NM_000025.3(ADRB3):c.785C>G (p.Pro262Arg)	ADRB3 (P262R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615720	NM_000025.3(ADRB3):c.784C>T (p.Pro262Ser)	ADRB3 (P262S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227003	NM_000025.3(ADRB3):c.767G>T (p.Arg256Leu)	ADRB3 (R256L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261366	NM_000025.3(ADRB3):c.742G>C (p.Glu248Gln)	ADRB3 (E248Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518602	NM_000025.3(ADRB3):c.697C>A (p.Arg233Ser)	ADRB3 (R233S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354689	NM_000025.3(ADRB3):c.692C>T (p.Ala231Val)	ADRB3 (A231V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384681	NM_000025.3(ADRB3):c.578C>G (p.Pro193Arg)	ADRB3 (P193R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560597	NM_000025.3(ADRB3):c.529T>C (p.Trp177Arg)	ADRB3 (W177R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091062	NM_000025.3(ADRB3):c.460G>T (p.Ala154Ser)	ADRB3 (A154S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1050272	NM_000025.3(ADRB3):c.452A>G (p.Lys151Arg)	ADRB3 (K151R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3091051	NM_000025.3(ADRB3):c.395C>A (p.Ala132Asp)	ADRB3 (A132D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486583	NM_000025.3(ADRB3):c.374T>C (p.Ile125Thr)	ADRB3 (I125T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604540	NM_000025.3(ADRB3):c.302G>T (p.Gly101Val)	ADRB3 (G101V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253399	NM_000025.3(ADRB3):c.202C>T (p.Leu68Phe)	ADRB3 (L68F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 17741	NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)	ADRB3 (W64R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3091031	NM_000025.3(ADRB3):c.169C>G (p.Leu57Val)	ADRB3 (L57V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338854	NM_000025.3(ADRB3):c.125C>A (p.Ala42Asp)	ADRB3 (A42D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715579	NM_000025.3(ADRB3):c.54C>G (p.Pro18=)	ADRB3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2223980	NM_000025.3(ADRB3):c.49C>T (p.Leu17Phe)	ADRB3 (L17F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218787	NM_000025.3(ADRB3):c.16C>T (p.His6Tyr)	ADRB3 (H6Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31