"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "GNB3"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1358406	NM_002075.4(GNB3):c.2T>C (p.Met1Thr)	GNB3 (M1T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2854737	NM_002075.4(GNB3):c.4G>A (p.Gly2Arg)	GNB3 (G2R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2907665	NM_002075.4(GNB3):c.5G>A (p.Gly2Glu)	GNB3 (G2E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1426267	NM_002075.4(GNB3):c.8A>G (p.Glu3Gly)	GNB3 (E3G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1399268	NM_002075.4(GNB3):c.11T>C (p.Met4Thr)	GNB3 (M4T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2044693	NM_002075.4(GNB3):c.22C>T (p.Arg8Cys)	GNB3 (R8C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 964467	NM_002075.4(GNB3):c.23G>A (p.Arg8His)	GNB3 (R8H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1061550	NM_002075.4(GNB3):c.28G>A (p.Glu10Lys)	GNB3 (E10K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1395424	NM_002075.4(GNB3):c.32C>T (p.Ala11Val)	GNB3 (A11V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2982846	NM_002075.4(GNB3):c.33G>T (p.Ala11=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1151061	NM_002075.4(GNB3):c.33G>A (p.Ala11=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2004458	NM_002075.4(GNB3):c.36G>C (p.Glu12Asp)	GNB3 (E12D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1105181	NM_002075.4(GNB3):c.39G>A (p.Gln13=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 853771	NM_002075.4(GNB3):c.41T>G (p.Leu14Arg)	GNB3 (L14R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125097	NM_002075.4(GNB3):c.45G>A (p.Lys15=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1007682	NM_002075.4(GNB3):c.56C>T (p.Ala19Val)	GNB3 (A19V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1943283	NM_002075.4(GNB3):c.57+6T>C	GNB3	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1668443	NM_002075.4(GNB3):c.57+14C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1938305	NM_002075.4(GNB3):c.57+19C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1022034	NM_002075.4(GNB3):c.58-25_60del	GNB3	Deletion (splice acceptor variant)	not provided	GUncertain significance
Select item 1636098	NM_002075.4(GNB3):c.58-19A>G	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1088613	NM_002075.4(GNB3):c.58-9T>C	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 850489	NM_002075.4(GNB3):c.73T>C (p.Cys25Arg)	GNB3 (C25R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 960328	NM_002075.4(GNB3):c.80A>G (p.Asp27Gly)	GNB3 (D27G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 748304	NM_002075.4(GNB3):c.81C>T (p.Asp27=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1022327	NM_002075.4(GNB3):c.82G>A (p.Val28Ile)	GNB3 (V28I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2120981	NM_002075.4(GNB3):c.89T>A (p.Leu30Gln)	GNB3 (L30Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2884547	NM_002075.4(GNB3):c.96+2T>G	GNB3	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 959220	NM_002075.4(GNB3):c.96+5G>T	GNB3	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1975058	NM_002075.4(GNB3):c.96+11dup	GNB3	Duplication (intron variant)	not provided	GBenign
Select item 1088346	NM_002075.4(GNB3):c.96+11C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1937060	NM_002075.4(GNB3):c.96+12del	GNB3	Deletion (intron variant)	not provided	GLikely benign
Select item 1641655	NM_002075.4(GNB3):c.96+15C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1133035	NM_002075.4(GNB3):c.96+16C>G	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1653050	NM_002075.4(GNB3):c.96+19C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1118616	NM_002075.4(GNB3):c.96+20G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2999377	NM_002075.4(GNB3):c.97-16G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1957762	NM_002075.4(GNB3):c.97-15C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1554621	NM_002075.4(GNB3):c.97-11T>C	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1545394	NM_002075.4(GNB3):c.97-9T>C	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1461987	NM_002075.4(GNB3):c.119T>C (p.Val40Ala)	GNB3 (V40A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2981176	NM_002075.4(GNB3):c.122G>A (p.Gly41Glu)	GNB3 (G41E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2735801	NM_002075.4(GNB3):c.124C>T (p.Arg42Ter)	GNB3 (R42*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2128706	NM_002075.4(GNB3):c.124C>G (p.Arg42Gly)	GNB3 (R42G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2825246	NM_002075.4(GNB3):c.127_133del (p.Val43fs)	GNB3 (V43fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1367277	NM_002075.4(GNB3):c.125G>A (p.Arg42Gln)	GNB3 (R42Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1663471	NM_002075.4(GNB3):c.129C>T (p.Val43=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1954095	NM_002075.4(GNB3):c.136C>T (p.Arg46Trp)	GNB3 (R46W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1005467	NM_002075.4(GNB3):c.137G>A (p.Arg46Gln)	GNB3 (R46Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2825247	NM_002075.4(GNB3):c.140_141insCACGGC (p.Thr47_Arg48insThrAla)	GNB3	Insertion (inframe_insertion)	not provided	GUncertain significance
Select item 960438	NM_002075.4(GNB3):c.140C>T (p.Thr47Met)	GNB3 (T47M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1168793	NM_002075.4(GNB3):c.141G>A (p.Thr47=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1006652	NM_002075.4(GNB3):c.142C>T (p.Arg48Trp)	GNB3 (R48W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1379768	NM_002075.4(GNB3):c.145C>T (p.Arg49Trp)	GNB3 (R49W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 943605	NM_002075.4(GNB3):c.146G>A (p.Arg49Gln)	GNB3 (R49Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1128604	NM_002075.4(GNB3):c.147G>A (p.Arg49=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1937606	NM_002075.4(GNB3):c.149C>T (p.Thr50Met)	GNB3 (T50M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1913763	NM_002075.4(GNB3):c.150G>A (p.Thr50=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2742762	NM_002075.4(GNB3):c.152T>A (p.Leu51Ter)	GNB3 (L51*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2012275	NM_002075.4(GNB3):c.169A>G (p.Lys57Glu)	GNB3 (K57E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1152745	NM_002075.4(GNB3):c.177C>T (p.Tyr59=)	GNB3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1370883	NM_002075.4(GNB3):c.178G>A (p.Ala60Thr)	GNB3 (A60T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946731	NM_002075.4(GNB3):c.186C>G (p.His62Gln)	GNB3 (H62Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1005493	NM_002075.4(GNB3):c.190G>A (p.Ala64Thr)	GNB3 (A64T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1904082	NM_002075.4(GNB3):c.192C>T (p.Ala64=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1000738	NM_002075.4(GNB3):c.193A>G (p.Thr65Ala)	GNB3 (T65A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 242986	NM_002075.4(GNB3):c.200C>T (p.Ser67Phe)	GNB3 (S67F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2096026	NM_002075.4(GNB3):c.203+6G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1113642	NM_002075.4(GNB3):c.203+9T>G	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1102352	NM_002075.4(GNB3):c.203+16dup	GNB3	Duplication (intron variant)	not provided	GLikely benign
Select item 2973564	NM_002075.4(GNB3):c.203+14_203+16del	GNB3	Deletion (intron variant)	not provided	GLikely benign
Select item 1951067	NM_002075.4(GNB3):c.203+10G>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1928926	NM_002075.4(GNB3):c.203+16del	GNB3	Deletion (intron variant)	not provided	GBenign
Select item 2789035	NM_002075.4(GNB3):c.203+11G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1645235	NM_002075.4(GNB3):c.203+11G>C	GNB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1604409	NM_002075.4(GNB3):c.203+11G>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667709	NM_002075.4(GNB3):c.203+12G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1654422	NM_002075.4(GNB3):c.203+12G>C	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1930389	NM_002075.4(GNB3):c.203+20C>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1639238	NM_002075.4(GNB3):c.203+20C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2023640	NM_002075.4(GNB3):c.204-19T>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1943835	NM_002075.4(GNB3):c.204-18G>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3023338	NM_002075.4(GNB3):c.211G>C (p.Val71Leu)	GNB3 (V71L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994875	NM_002075.4(GNB3):c.221C>T (p.Ser74Leu)	GNB3 (S74L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1060059	NM_002075.4(GNB3):c.221C>G (p.Ser74Trp)	GNB3 (S74W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1093312	NM_002075.4(GNB3):c.222G>A (p.Ser74=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 938456	NM_002075.4(GNB3):c.226G>T (p.Asp76Tyr)	GNB3 (D76Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1626337	NM_002075.4(GNB3):c.240C>T (p.Ile80=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 945400	NM_002075.4(GNB3):c.241G>A (p.Val81Met)	GNB3 (V81M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1089283	NM_002075.4(GNB3):c.249C>T (p.Asp83=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1966695	NM_002075.4(GNB3):c.255C>G (p.Tyr85Ter)	GNB3 (Y85*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1376204	NM_002075.4(GNB3):c.261CAA[1] (p.Asn88del)	GNB3 (N88del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1713950	NM_002075.4(GNB3):c.263A>G (p.Asn88Ser)	GNB3 (N88S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 969193	NM_002075.4(GNB3):c.263A>C (p.Asn88Thr)	GNB3 (N88T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1153865	NM_002075.4(GNB3):c.264C>T (p.Asn88=)	GNB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2126567	NM_002075.4(GNB3):c.267+8C>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1936905	NM_002075.4(GNB3):c.267+8C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1654484	NM_002075.4(GNB3):c.267+12G>C	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2786392	NM_002075.4(GNB3):c.267+18C>A	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1578684	NM_002075.4(GNB3):c.268-6C>T	GNB3	Single nucleotide variant (intron variant)	not provided	GLikely benign

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