"Ambry Genetics"[submitter] AND "ARRB2"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2335097	NM_004313.4(ARRB2):c.38C>T (p.Ser13Leu)	ARRB2 (S13L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316188	NM_004313.4(ARRB2):c.43C>T (p.Pro15Ser)	ARRB2 (P15S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316167	NM_004313.4(ARRB2):c.179G>C (p.Cys60Ser)	ARRB2 (C45S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2554319	NM_004313.4(ARRB2):c.287G>A (p.Arg96Gln)	ARRB2 (R96Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2538239	NM_004313.4(ARRB2):c.340C>A (p.His114Asn)	ARRB2 (H99N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2476814	NM_004313.4(ARRB2):c.443G>A (p.Arg148Gln)	ARRB2, LOC132090475 (R169Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129844	NM_004313.4(ARRB2):c.515T>C (p.Val172Ala)	ARRB2 (V157A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3316198	NM_004313.4(ARRB2):c.565C>T (p.Arg189Cys)	ARRB2 (R210C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3316178	NM_004313.4(ARRB2):c.587G>A (p.Arg196Gln)	ARRB2 (R4Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554697	NM_004313.4(ARRB2):c.617A>G (p.Lys206Arg)	ARRB2 (K227R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508480	NM_004313.4(ARRB2):c.647A>G (p.Asn216Ser)	ARRB2, LOC126862469 (N24S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2293938	NM_004313.4(ARRB2):c.747G>T (p.Gln249His)	ARRB2, LOC126862469 (Q57H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338069	NM_004313.4(ARRB2):c.847C>T (p.Arg283Trp)	ARRB2, LOC126862469 (R283W +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3316158	NM_004313.4(ARRB2):c.899A>G (p.Asn300Ser)	ARRB2, LOC126862469 (N285S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2589182	NM_004313.4(ARRB2):c.918C>T (p.Ile306=)	ARRB2 (R263C)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 3316147	NM_004313.4(ARRB2):c.925G>C (p.Glu309Gln)	ARRB2 (E117Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129846	NM_004313.4(ARRB2):c.992C>T (p.Ser331Phe)	ARRB2 (S331F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2270362	NM_004313.4(ARRB2):c.1061C>T (p.Pro354Leu)	ARRB2 (P375L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2568586	NM_004313.4(ARRB2):c.1063C>T (p.Leu355Phe)	ARRB2 (L340F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129843	NM_004313.4(ARRB2):c.1084G>A (p.Ala362Thr)	ARRB2 (A359T +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528030	NM_004313.4(ARRB2):c.1099G>A (p.Val367Ile)	ARRB2 (V367I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364747	NM_004313.4(ARRB2):c.1145C>T (p.Thr382Ile)	ARRB2 (T190I +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2314597	NM_004313.4(ARRB2):c.1216G>A (p.Asp406Asn)	ARRB2 (D427N +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 23