ClinVar for Gene (Select 5468) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3371895	NM_138711.6(PPARG):c.1415dup (p.Asp473fs)	PPARG (D264fs +2 more)	Duplication (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 3368902	NM_138711.6(PPARG):c.425T>C (p.Ile142Thr)	PPARG (I142T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3358997	NM_138711.6(PPARG):c.221-1G>C	PPARG	Single nucleotide variant (splice acceptor variant)	PPARG-related familial partial lipodystrophy	GPathogenic
Select item 3358792	NM_138711.6(PPARG):c.729+35C>T	LOC114803475, PPARG (A257V +1 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3357803	NM_138711.6(PPARG):c.-8-28084A>G	PPARG (I10V)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3357781	NM_138711.6(PPARG):c.1228A>C (p.Asn410His)	PPARG (N201H +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3357661	NM_138711.6(PPARG):c.288T>C (p.Pro96=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3357560	NM_138711.6(PPARG):c.1386T>G (p.Ser462Arg)	PPARG (S253R +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3357299	NM_138711.6(PPARG):c.102C>T (p.Pro34=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3357147	NM_138711.6(PPARG):c.492G>T (p.Arg164=)	PPARG (G22V)	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3357132	NM_138711.6(PPARG):c.1329T>A (p.Ile443=)	PPARG	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3357036	NM_138711.6(PPARG):c.1016T>C (p.Ile339Thr)	PPARG (I130T +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3356831	NM_138711.6(PPARG):c.7G>A (p.Asp3Asn)	PPARG (D33N +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3356818	NM_138711.6(PPARG):c.405A>G (p.Arg135=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3356734	NM_138711.6(PPARG):c.391-7T>C	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3356360	NM_138711.6(PPARG):c.674C>T (p.Pro225Leu)	LOC114803475, PPARG (P225L +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3356135	NM_138711.6(PPARG):c.435A>T (p.Arg145Ser)	PPARG (D3V +3 more)	Single nucleotide variant (missense variant)	PPARG-related disorder	GUncertain significance
Select item 3356072	NM_138711.6(PPARG):c.408A>T (p.Thr136=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3355769	NM_138711.6(PPARG):c.529+10C>T	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3355631	NM_138711.6(PPARG):c.*7G>C	PPARG	Single nucleotide variant (3 prime UTR variant)	PPARG-related disorder	GLikely benign
Select item 3355059	NM_138711.6(PPARG):c.954T>C (p.Tyr318=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3355020	NM_138711.6(PPARG):c.-8-28073A>G	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3354506	NM_138711.6(PPARG):c.-8-28111A>G	PPARG (M1V)	Single nucleotide variant (missense variant +2 more)	PPARG-related disorder	GUncertain significance
Select item 3354140	NM_138711.6(PPARG):c.1089G>A (p.Glu363=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3353707	NM_138711.6(PPARG):c.300T>C (p.Pro100=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3353211	NM_138711.6(PPARG):c.901A>G (p.Ile301Val)	PPARG (I301V +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3353130	NM_138711.6(PPARG):c.37T>C (p.Phe13Leu)	PPARG (F13L +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3352879	NM_138711.6(PPARG):c.1314A>C (p.Thr438=)	PPARG	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3352409	NM_138711.6(PPARG):c.1270C>G (p.Pro424Ala)	PPARG (P215A +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3351893	NM_138711.6(PPARG):c.810G>A (p.Glu270=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351756	NM_138711.6(PPARG):c.885A>G (p.Thr295=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351622	NM_138711.6(PPARG):c.930C>T (p.Asn310=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351332	NM_138711.6(PPARG):c.925T>C (p.Leu309=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351301	NM_138711.6(PPARG):c.735C>T (p.Phe245=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351222	NM_138711.6(PPARG):c.-8-28064C>T	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3351188	NM_138711.6(PPARG):c.184G>A (p.Asp62Asn)	PPARG (D62N +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3351146	NM_138711.6(PPARG):c.711A>G (p.Gly237=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3350867	NM_138711.6(PPARG):c.313A>G (p.Met105Val)	PPARG (M105V +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3350744	NM_138711.6(PPARG):c.530-9C>T	LOC114803475, PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3350626	NM_138711.6(PPARG):c.133A>C (p.Thr45Pro)	PPARG (T45P +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3350612	NM_138711.6(PPARG):c.801C>A (p.Pro267=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3350024	NM_138711.6(PPARG):c.-8A>G	PPARG (E28G)	Single nucleotide variant (5 prime UTR variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3349626	NM_138711.6(PPARG):c.-8-28119A>T	PPARG	Single nucleotide variant (5 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3348870	NM_138711.6(PPARG):c.291T>C (p.His97=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3348779	NM_138711.6(PPARG):c.800C>A (p.Pro267His)	PPARG (P267H +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3348314	NM_138711.6(PPARG):c.-8-17T>G	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3347032	NM_138711.6(PPARG):c.-8-28083T>C	PPARG (I10T)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3346683	NM_138711.6(PPARG):c.154C>G (p.Pro52Ala)	PPARG (P52A +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3345678	NM_138711.6(PPARG):c.275T>C (p.Leu92Pro)	PPARG (L122P +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3345593	NM_138711.6(PPARG):c.729+34G>A	LOC114803475, PPARG (A257T +1 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3344424	NM_138711.6(PPARG):c.-8-28078C>A	PPARG (P12T)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3344158	NM_138711.6(PPARG):c.-8-28051C>G	PPARG (L21V)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3344116	NM_138711.6(PPARG):c.561G>C (p.Glu187Asp)	LOC114803475, PPARG (E187D +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3340491	NM_138711.6(PPARG):c.346dup (p.Ala116fs)	PPARG (A116fs +2 more)	Duplication (frameshift variant +1 more)	PPARG-related familial partial lipodystrophy +1 more	GLikely pathogenic
Select item 3247023	NC_000003.11:g.(?_12447361)_(12458673_?)del	PPARG	Deletion	not provided	GUncertain significance
Select item 3242334	GRCh37/hg19 3p26.3-22.3(chr3:60000-34461438)x3	ANKRD28, ARL8B +145 more	Copy number gain	not provided	GPathogenic
Select item 3217014	NM_138711.6(PPARG):c.133A>G (p.Thr45Ala)	PPARG (T47A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3062708	GRCh37/hg19 3p26.3-22.3(chr3:61891-33946644)x3	OXTR, PDCD6IP +145 more	Copy number gain	not specified	GPathogenic
Select item 3061592	NM_138711.6(PPARG):c.530-7T>A	LOC114803475, PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3057846	NM_138711.6(PPARG):c.993G>C (p.Leu331Phe)	PPARG (L122F +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3057658	NM_138711.6(PPARG):c.618C>T (p.Ser206=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3057367	NM_138711.6(PPARG):c.273G>A (p.Gln91=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3054277	NM_138711.6(PPARG):c.693G>C (p.Ala231=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3051279	NM_138711.6(PPARG):c.132T>A (p.Ser44=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3049705	NM_138711.6(PPARG):c.1266C>T (p.Asn422=)	PPARG	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3048704	NM_138711.6(PPARG):c.1140C>T (p.Ser380=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3048376	NM_138711.6(PPARG):c.-8-14A>G	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3044120	NM_138711.6(PPARG):c.*3G>A	PPARG	Single nucleotide variant (3 prime UTR variant)	PPARG-related disorder	GLikely benign
Select item 3043338	NM_138711.6(PPARG):c.1181-6C>A	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3042755	NM_138711.6(PPARG):c.729+36G>A	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3040523	NM_138711.6(PPARG):c.729+25T>C	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3039994	NM_138711.6(PPARG):c.441T>C (p.Asp147=)	PPARG (I5T)	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3037104	NM_138711.6(PPARG):c.391-6T>C	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3036791	NM_138711.6(PPARG):c.801C>T (p.Pro267=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3035411	NM_138711.6(PPARG):c.243A>G (p.Ala81=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3033685	NM_138711.6(PPARG):c.729+73G>A	LOC114803475, PPARG	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3031383	NM_138711.6(PPARG):c.1181-10G>T	PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3024551	NM_138711.6(PPARG):c.551C>T (p.Pro184Leu)	PPARG, LOC114803475 (P184L +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related familial partial lipodystrophy	GPathogenic
Select item 3024550	NM_138711.6(PPARG):c.443T>C (p.Leu148Pro)	PPARG (L148P +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related familial partial lipodystrophy	GPathogenic
Select item 3023898	NM_138711.6(PPARG):c.220+15T>C	PPARG	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004774	NM_138711.6(PPARG):c.57T>G (p.Asp19Glu)	PPARG (D19E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2984411	NM_138711.6(PPARG):c.457C>T (p.His153Tyr)	PPARG (H155Y +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2974355	NM_138711.6(PPARG):c.958G>A (p.Val320Ile)	PPARG (V350I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2970223	NM_138711.6(PPARG):c.-8-28079C>T	PPARG	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2910165	NM_138711.6(PPARG):c.692C>A (p.Ala231Glu)	LOC114803475, PPARG (A233E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2893058	NM_138711.6(PPARG):c.619G>A (p.Ala207Thr)	LOC114803475, PPARG (A237T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2878857	NM_138711.6(PPARG):c.-8-28026A>C	PPARG	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2877096	NM_138711.6(PPARG):c.391-5dup	PPARG	Duplication (intron variant)	not provided	GLikely benign
Select item 2867439	NM_138711.6(PPARG):c.1057_1058delinsGA (p.Ser353Asp)	PPARG (S383D +2 more)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 2844285	NM_138711.6(PPARG):c.389A>T (p.Lys130Met)	PPARG (K132M +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2818280	NM_138711.6(PPARG):c.1343T>G (p.Val448Gly)	PPARG (V239G +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2780020	NM_138711.6(PPARG):c.983T>C (p.Leu328Pro)	PPARG (L328P +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2780019	NM_138711.6(PPARG):c.359A>G (p.His120Arg)	PPARG (H120R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2766535	NM_138711.6(PPARG):c.1084A>G (p.Met362Val)	PPARG (M153V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2755604	NM_138711.6(PPARG):c.312C>G (p.Leu104=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2734443	NM_138711.6(PPARG):c.598G>A (p.Asp200Asn)	LOC114803475, PPARG (D230N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2734442	NM_138711.6(PPARG):c.329G>A (p.Arg110His)	PPARG (R112H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2719983	NM_138711.6(PPARG):c.99G>A (p.Lys33=)	PPARG	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2718555	NM_138711.6(PPARG):c.698C>T (p.Ala233Val)	LOC114803475, PPARG (A263V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2702286	NM_138711.6(PPARG):c.1180+13T>G	PPARG	Single nucleotide variant (intron variant)	not provided	GLikely benign

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