ClinVar for Gene (Select 150763) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282046	NM_001321527.2(GPAT2):c.2113A>G (p.Lys705Glu)	GPAT2 (K628E +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3282045	NM_001321527.2(GPAT2):c.2254G>A (p.Ala752Thr)	GPAT2 (A746T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3282044	NM_001321527.2(GPAT2):c.1346A>C (p.His449Pro)	GPAT2 (H378P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282043	NM_001321527.2(GPAT2):c.2240C>T (p.Ala747Val)	GPAT2 (R637W +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282042	NM_001321527.2(GPAT2):c.2386C>T (p.Arg796Trp)	GPAT2 (R719W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282041	NM_001321527.2(GPAT2):c.1906G>A (p.Ala636Thr)	GPAT2 (A636T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282040	NM_001321527.2(GPAT2):c.2387G>A (p.Arg796Gln)	GPAT2 (R790Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282039	NM_001321527.2(GPAT2):c.1564G>A (p.Val522Met)	GPAT2 (V445M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242291	GRCh37/hg19 2q11.1-11.2(chr2:96555654-98024790)x1	ADRA2B, ANKRD23 +21 more	Copy number loss	not provided	GUncertain significance
Select item 3101124	NM_001321527.2(GPAT2):c.481G>C (p.Val161Leu)	GPAT2 (V161L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3101123	NM_001321527.2(GPAT2):c.2387G>C (p.Arg796Pro)	GPAT2 (R725P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101122	NM_001321527.2(GPAT2):c.2303C>T (p.Thr768Met)	GPAT2 (T691M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3101121	NM_001321527.2(GPAT2):c.2291T>G (p.Val764Gly)	GPAT2 (V687G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101120	NM_001321527.2(GPAT2):c.2279G>C (p.Arg760Thr)	GPAT2 (E670Q +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101119	NM_001321527.2(GPAT2):c.2198T>G (p.Phe733Cys)	GPAT2 (S730A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101118	NM_001321527.2(GPAT2):c.2176T>C (p.Tyr726His)	GPAT2 (Y649H +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3101117	NM_001321527.2(GPAT2):c.2143C>T (p.Arg715Cys)	GPAT2 (R715C +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3101116	NM_001321527.2(GPAT2):c.2086C>T (p.Leu696Phe)	GPAT2 (L690F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3101115	NM_001321527.2(GPAT2):c.2063A>G (p.His688Arg)	GPAT2 (H617R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3101114	NM_001321527.2(GPAT2):c.2045G>C (p.Arg682Thr)	GPAT2 (R611T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101113	NM_001321527.2(GPAT2):c.1724C>T (p.Pro575Leu)	GPAT2 (P504L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101112	NM_001321527.2(GPAT2):c.1675G>A (p.Glu559Lys)	GPAT2 (E488K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101110	NM_001321527.2(GPAT2):c.1663G>A (p.Val555Ile)	GPAT2 (V549I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101109	NM_001321527.2(GPAT2):c.1502T>C (p.Val501Ala)	GPAT2 (V495A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101107	NM_001321527.2(GPAT2):c.1078C>T (p.Arg360Cys)	GPAT2 (R360C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062352	Single allele	ADRA2B, ASTL +4 more	Deletion	Pheochromocytoma	GUncertain significance
Select item 3024512	NM_001321527.2(GPAT2):c.1879C>T (p.Arg627Trp)	GPAT2 (R550W +3 more)	Single nucleotide variant (missense variant +1 more)	Male infertility	GLikely pathogenic
Select item 3024511	NM_001321527.2(GPAT2):c.1388C>T (p.Thr463Met)	GPAT2 (T392M +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 3024510	NM_001321527.2(GPAT2):c.1130A>G (p.His377Arg)	GPAT2 (H306R +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 3024509	NM_001321527.2(GPAT2):c.1954C>T (p.Arg652Ter)	GPAT2 (R575* +3 more)	Single nucleotide variant (nonsense +1 more)	Male infertility	GLikely pathogenic
Select item 3024503	NM_001321527.2(GPAT2):c.1156-1G>A	GPAT2	Single nucleotide variant (splice acceptor variant)	Male infertility	GLikely pathogenic
Select item 3024492	NM_001321527.2(GPAT2):c.146G>A (p.Arg49His)	GPAT2 (R49H)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 2685857	GRCh37/hg19 2q11.1-11.2(chr2:95773428-102550061)x3	ACTR1B, ADRA2B +64 more	Copy number gain	not provided	GLikely pathogenic
Select item 2671593	Single allele	ADRA2B, ANKRD23 +20 more	Deletion	not provided	GUncertain significance
Select item 2651137	NM_001321527.2(GPAT2):c.78G>A (p.Ser26=)	GPAT2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2651136	NM_001321527.2(GPAT2):c.126G>A (p.Lys42=)	GPAT2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2618330	NM_001321527.2(GPAT2):c.1674C>G (p.Ser558Arg)	GPAT2 (S552R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597491	NM_001321527.2(GPAT2):c.2390A>G (p.Gln797Arg)	GPAT2 (Q726R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535907	NM_001321527.2(GPAT2):c.1385G>A (p.Ser462Asn)	GPAT2 (S391N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530361	NM_001321527.2(GPAT2):c.1980A>C (p.Lys660Asn)	GPAT2 (K660N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524810	NM_001321527.2(GPAT2):c.2032G>A (p.Gly678Ser)	GPAT2 (G678S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512220	NM_001321527.2(GPAT2):c.134C>T (p.Pro45Leu)	GPAT2 (P45L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509930	NM_001321527.2(GPAT2):c.2368A>C (p.Lys790Gln)	GPAT2 (K719Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494385	NM_001321527.2(GPAT2):c.1667T>C (p.Phe556Ser)	GPAT2 (F550S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484323	NM_001321527.2(GPAT2):c.2390A>C (p.Gln797Pro)	GPAT2 (Q720P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478682	NM_001321527.2(GPAT2):c.2154G>T (p.Gln718His)	GPAT2 (Q712H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2478681	NM_001321527.2(GPAT2):c.1328T>A (p.Val443Asp)	GPAT2 (V372D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473228	NM_001321527.2(GPAT2):c.2206G>A (p.Ala736Thr)	GPAT2 (A736T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2470833	NM_001321527.2(GPAT2):c.36G>C (p.Gln12His)	GPAT2 (Q12H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468872	NM_001321527.2(GPAT2):c.1555C>T (p.Arg519Trp)	GPAT2 (R519W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369535	NM_001321527.2(GPAT2):c.2234A>C (p.Glu745Ala)	GPAT2 (E668A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354576	NM_001321527.2(GPAT2):c.1700G>A (p.Arg567Gln)	GPAT2 (R567Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330344	NM_001321527.2(GPAT2):c.1861T>C (p.Cys621Arg)	GPAT2 (C621R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325383	NM_001321527.2(GPAT2):c.2083T>C (p.Phe695Leu)	GPAT2 (F689L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2310571	NM_001321527.2(GPAT2):c.1793T>C (p.Leu598Pro)	GPAT2 (L527P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253593	NM_001321527.2(GPAT2):c.1784G>A (p.Arg595His)	GPAT2 (R524H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235493	NM_001321527.2(GPAT2):c.2212G>A (p.Ala738Thr)	GPAT2 (A661T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2223743	NM_001321527.2(GPAT2):c.1582C>T (p.Arg528Cys)	GPAT2 (R457C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220929	NM_001321527.2(GPAT2):c.1355G>C (p.Ser452Thr)	GPAT2 (S452T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219377	NM_001321527.2(GPAT2):c.1522C>T (p.Arg508Trp)	GPAT2 (R431W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205653	NM_001321527.2(GPAT2):c.2039A>G (p.Tyr680Cys)	GPAT2 (Y674C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1808615	GRCh37/hg19 2q11.1-11.2(chr2:95341388-100340514)x3	ACTR1B, ADRA2B +54 more	Copy number gain	not provided	GLikely pathogenic
Select item 1807978	GRCh37/hg19 2q11.1-11.2(chr2:96628608-96981369)x3	ADRA2B, ANKRD36C +7 more	Copy number gain	not provided	GUncertain significance
Select item 1708190	GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	ACTG2, ACTR1B +529 more	Copy number loss	See cases	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1526874	GRCh37/hg19 2q11.1(chr2:95341387-96735978)	ANKRD36C, FAHD2A +10 more	Copy number loss	not specified	GUncertain significance
Select item 1340229	GRCh37/hg19 2q11.1-11.2(chr2:96544603-98025634)x3	ADRA2B, ANKRD23 +21 more	Copy number gain	not provided	GUncertain significance
Select item 980467	GRCh37/hg19 2q11.1-11.2(chr2:96544602-97706860)x3	ADRA2B, ANKRD23 +19 more	Copy number gain	not provided	GUncertain significance
Select item 980466	GRCh37/hg19 2q11.1-11.2(chr2:96421161-97765561)x1	ASTL, CIAO1 +20 more	Copy number loss	not provided	GUncertain significance
Select item 980465	GRCh37/hg19 2q11.1-11.2(chr2:96515883-98162176)x3	ARID5A, ASTL +22 more	Copy number gain	not provided	GUncertain significance
Select item 980464	GRCh37/hg19 2q11.1-11.2(chr2:96630256-96836549)x3	ANKRD36C, DUSP2 +3 more	Copy number gain	not provided	GLikely benign
Select item 814282	GRCh37/hg19 2q11.1(chr2:96152644-96747884)x3	GPAT2, TRIM43 +1 more	Copy number gain	not provided	GLikely benign
Select item 813848	GRCh37/hg19 2q11.1(chr2:95945437-96259086)x3	KCNIP3, PROM2 +5 more	Copy number gain	Autism +1 more	GUncertain significance
Select item 771336	NM_001321527.2(GPAT2):c.135C>T (p.Pro45=)	GPAT2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 687873	GRCh37/hg19 2q11.1-11.2(chr2:96552903-98118115)x1	ADRA2B, ANKRD23 +21 more	Copy number loss	not provided	GPathogenic
Select item 685047	GRCh37/hg19 2q11.1-11.2(chr2:96515883-98025634)x3	ASTL, CIAO1 +21 more	Copy number gain	not provided	GUncertain significance
Select item 562679	GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3	C2orf15, C2orf49 +122 more	Copy number gain	not provided	GPathogenic
Select item 562643	GRCh37/hg19 2q11.1-11.2(chr2:96544602-98138405)x1	ADRA2B, ANKRD23 +22 more	Copy number loss	not provided	GUncertain significance
Select item 562639	GRCh37/hg19 2q11.1(chr2:95341387-96719347)x1	ANKRD36C, FAHD2A +10 more	Copy number loss	not provided	GUncertain significance
Select item 524189	Single allele	ACMSD, C2orf27A +486 more	Deletion	not provided	GLikely pathogenic
Select item 443435	GRCh37/hg19 2q11.1-11.2(chr2:96468158-97871906)x3	ADRA2B, ANKRD23 +21 more	Copy number gain	See cases	GLikely pathogenic
Select item 443415	GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127)	ACTR1B, ADRA2B +86 more	Copy number gain	See cases	GUncertain significance
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 441953	GRCh37/hg19 2q11.1-11.2(chr2:96097383-97679933)x1	ADRA2B, ANKRD23 +21 more	Copy number loss	See cases	GUncertain significance
Select item 395690	GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266)	ACTR1B, ADRA2B +88 more	Copy number gain	See cases	GPathogenic
Select item 395484	GRCh37/hg19 2q11.1-11.2(chr2:96698012-97757442)x3	ADRA2B, ANKRD23 +19 more	Copy number gain	See cases	GUncertain significance
Select item 394206	GRCh37/hg19 2q11.1-11.2(chr2:95691600-100587394)	AFF3, ADRA2B +53 more	Copy number gain	See cases	GPathogenic
Select item 160960	GRCh38/hg38 2q11.1-11.2(chr2:95879602-97029672)x3	ADRA2B, ANKRD23 +119 more	Copy number gain	See cases	GUncertain significance
Select item 152537	GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3	ACTR1B, ADRA2B +550 more	Copy number gain	See cases	GPathogenic
Select item 151425	GRCh38/hg38 2q11.2(chr2:96006224-96039305)x3	GPAT2	Copy number gain	See cases	GBenign
Select item 148950	GRCh38/hg38 2q11.1-11.2(chr2:95337458-99072953)x3	ACTR1B, ADRA2B +207 more	Copy number gain	See cases	GUncertain significance
Select item 148751	GRCh38/hg38 2q11.1-11.2(chr2:95766541-97589743)x3	ADRA2B, ANKRD23 +131 more	Copy number gain	See cases	GUncertain significance
Select item 145754	GRCh38/hg38 2q11.1-11.2(chr2:95674981-96052275)x3	ANKRD36C, GPAT2 +6 more	Copy number gain	See cases	GBenign
Select item 144712	GRCh38/hg38 2q11.1-11.2(chr2:95879602-97029672)x1	ADRA2B, ANKRD23 +119 more	Copy number loss	See cases	GPathogenic
Select item 144357	GRCh38/hg38 2q11.1-11.2(chr2:95493468-96977610)x3	ADRA2B, ANKRD23 +126 more	Copy number gain	See cases	GUncertain significance
Select item 59311	GRCh38/hg38 2q11.1-11.2(chr2:95916534-97024341)x3	ADRA2B, ANKRD23 +119 more	Copy number gain	See cases	GUncertain significance
Select item 59310	GRCh38/hg38 2q11.1-11.2(chr2:95880668-97131646)x3	LOC129934346, LOC129934347 +125 more	Copy number gain	See cases	GUncertain significance
Select item 59309	GRCh38/hg38 2q11.1-11.2(chr2:95810453-97024341)x3	ADRA2B, ANKRD23 +120 more	Copy number gain	See cases	GUncertain significance
Select item 59308	GRCh38/hg38 2q11.1-11.2(chr2:95806265-97285797)x3	ADRA2B, ANKRD23 +127 more	Copy number gain	See cases	GUncertain significance

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