"GeneDx"[submitter] AND "PTPRO"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58986	GRCh38/hg38 12p13.2-12.3(chr12:12388842-15540422)x1	APOLD1, ARHGDIB +140 more	Copy number loss	See cases	GPathogenic
Select item 1707139	NC_000012.12:g.15322059AC[5]	PTPRO	Microsatellite	not provided	GLikely benign
Select item 1269902	NC_000012.12:g.15322293G>A	PTPRO	Single nucleotide variant	not provided	GBenign
Select item 1315836	NM_030667.3(PTPRO):c.76-109A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1234355	NM_030667.3(PTPRO):c.108T>C (p.Asp36=)	PTPRO	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1183685	NM_030667.3(PTPRO):c.349+155C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235789	NM_030667.3(PTPRO):c.349+211C>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262483	NM_030667.3(PTPRO):c.349+219T>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174249	NM_030667.3(PTPRO):c.350-280T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316651	NM_030667.3(PTPRO):c.508+19G>A	PTPRO	Single nucleotide variant (intron variant)	Nephrotic syndrome, type 6 +1 more	GBenign/Likely benign
Select item 1175500	NM_030667.3(PTPRO):c.509-156A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239607	NM_030667.3(PTPRO):c.509-46T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245257	NM_030667.3(PTPRO):c.661+123T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282198	NM_030667.3(PTPRO):c.661+284T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226652	NM_030667.3(PTPRO):c.662-165T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 708124	NM_030667.3(PTPRO):c.682A>G (p.Ile228Val)	PTPRO (I228V)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1329719	NM_030667.3(PTPRO):c.1105+29A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1258322	NM_030667.3(PTPRO):c.1105+160T>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 981947	NM_030667.3(PTPRO):c.1106-10T>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1315691	NM_030667.3(PTPRO):c.1110C>G (p.Asn370Lys)	PTPRO (N370K)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1267743	NM_030667.3(PTPRO):c.1268-281A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269172	NM_030667.3(PTPRO):c.1268-263A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224025	NM_030667.3(PTPRO):c.1268-231G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268385	NM_030667.3(PTPRO):c.1268-64A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 773660	NM_030667.3(PTPRO):c.1327G>A (p.Val443Ile)	PTPRO (V443I)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1272147	NM_030667.3(PTPRO):c.1464+269T>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317793	NM_030667.3(PTPRO):c.1464+278G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1277252	NM_030667.3(PTPRO):c.1464+284G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220914	NM_030667.3(PTPRO):c.1465-280G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316450	NM_030667.3(PTPRO):c.1585+90G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1227818	NM_030667.3(PTPRO):c.1586-283AG[2]	PTPRO	Microsatellite (intron variant)	not provided	GBenign
Select item 1316652	NM_030667.3(PTPRO):c.1586-241del	PTPRO	Deletion (intron variant)	not provided	GLikely benign
Select item 1238297	NM_030667.3(PTPRO):c.1586-244AAAAG[4]	PTPRO	Microsatellite (intron variant)	not provided	GBenign
Select item 1223304	NM_030667.3(PTPRO):c.1586-200G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257478	NM_030667.3(PTPRO):c.1586-152_1586-145dup	PTPRO	Duplication (intron variant)	not provided	GBenign
Select item 1288137	NM_030667.3(PTPRO):c.1586-145dup	PTPRO	Duplication (intron variant)	not provided	GBenign
Select item 1275159	NM_030667.3(PTPRO):c.1586-144A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225312	NM_030667.3(PTPRO):c.1586-144_1586-143insGGAAGGG	PTPRO	Insertion (intron variant)	not provided	GBenign
Select item 1318287	NM_030667.3(PTPRO):c.1586-124G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1246033	NM_030667.3(PTPRO):c.1586-112T>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174741	NM_030667.3(PTPRO):c.1626T>C (p.Gly542=)	PTPRO	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1266511	NM_030667.3(PTPRO):c.1779+290A>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273643	NM_030667.3(PTPRO):c.1779+298T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241124	NM_030667.3(PTPRO):c.1780-32C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317537	NM_030667.3(PTPRO):c.1892-177_1892-176insTAT	PTPRO	Insertion (intron variant)	not provided	GLikely benign
Select item 1317263	NM_030667.3(PTPRO):c.1892-173_1892-172insCTTGTTGTA	PTPRO	Insertion (intron variant)	not provided	GLikely benign
Select item 1317264	NM_030667.3(PTPRO):c.1892-58G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 668247	NM_030667.3(PTPRO):c.1973C>T (p.Thr658Met)	PTPRO (T658M)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1274669	NM_030667.3(PTPRO):c.2043+93A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317265	NM_030667.3(PTPRO):c.2043+151G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1236216	NM_030667.3(PTPRO):c.2043+239A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317817	NM_030667.3(PTPRO):c.2044-241A>C	LOC126861467, PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1258356	NM_030667.3(PTPRO):c.2088C>A (p.Gly696=)	LOC126861467, PTPRO	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 777233	NM_030667.3(PTPRO):c.2100C>T (p.Asn700=)	LOC126861467, PTPRO	Single nucleotide variant (synonymous variant)	Nephrotic syndrome, type 6 +1 more	GBenign/Likely benign
Select item 1263305	NM_030667.3(PTPRO):c.2164+12G>A	LOC126861467, PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318024	NM_030667.3(PTPRO):c.2165-266T>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316449	NM_030667.3(PTPRO):c.2165-5C>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 710130	NM_030667.3(PTPRO):c.2256T>C (p.Phe752=)	PTPRO	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1288391	NM_030667.3(PTPRO):c.2304+130C>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224172	NM_030667.3(PTPRO):c.2305-176G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245638	NM_030667.3(PTPRO):c.2305-21C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317311	NM_030667.3(PTPRO):c.2437+19_2437+20insAAA	PTPRO	Insertion (intron variant)	not provided	GLikely benign
Select item 1317591	NM_030667.3(PTPRO):c.2437+20_2437+21insCTGGTCTTTGGAAGTTCTTTCCATATTTTTTTCC	PTPRO	Insertion (intron variant)	not provided	GLikely benign
Select item 1317313	NM_030667.3(PTPRO):c.2437+24A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2571816	NM_030667.3(PTPRO):c.2437+43AT[7]	PTPRO	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1281543	NM_030667.3(PTPRO):c.2438-335G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317310	NM_030667.3(PTPRO):c.2438-199C>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1223888	NM_030667.3(PTPRO):c.2438-60G>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317312	NM_030667.3(PTPRO):c.2558+328A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1281753	NM_030667.3(PTPRO):c.2559-119C>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221741	NM_030667.3(PTPRO):c.2628-70A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317908	NM_030667.3(PTPRO):c.2712-157T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1245259	NM_030667.3(PTPRO):c.2712-140_2712-139insTTAA	PTPRO	Insertion (intron variant)	not provided	GBenign
Select item 1316624	NM_030667.3(PTPRO):c.2712-92T>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1242755	NM_030667.3(PTPRO):c.2747+199A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316626	NM_030667.3(PTPRO):c.2748-273T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316625	NM_030667.3(PTPRO):c.2748-105C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1233425	NM_030667.3(PTPRO):c.2829+123A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275425	NM_030667.3(PTPRO):c.2829+243C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1180371	NM_030667.3(PTPRO):c.2830-254T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235662	NM_030667.3(PTPRO):c.2830-248T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226629	NM_030667.3(PTPRO):c.2830-63_2830-62insG	PTPRO	Insertion (intron variant)	not provided	GBenign
Select item 1237351	NM_030667.3(PTPRO):c.2830-43C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 773260	NM_030667.3(PTPRO):c.2841G>A (p.Leu947=)	PTPRO	Single nucleotide variant (synonymous variant)	Nephrotic syndrome, type 6 +1 more	GBenign/Likely benign
Select item 1280504	NM_030667.3(PTPRO):c.2921-18T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296883	NM_030667.3(PTPRO):c.2997+67T>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1177885	NM_030667.3(PTPRO):c.2997+200A>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1317470	NM_030667.3(PTPRO):c.2997+223G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317314	NM_030667.3(PTPRO):c.2997+227A>G	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317948	NM_030667.3(PTPRO):c.2998-204A>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1258706	NM_030667.3(PTPRO):c.3036G>A (p.Gly1012=)	PTPRO	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1320626	NM_030667.3(PTPRO):c.3132+133G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1257268	NM_030667.3(PTPRO):c.3132+147A>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236701	NM_030667.3(PTPRO):c.3133-327G>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252582	NM_030667.3(PTPRO):c.3133-134_3133-133insGTATT	PTPRO	Insertion (intron variant)	not provided	GBenign
Select item 1234791	NM_030667.3(PTPRO):c.3255+65G>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257405	NM_030667.3(PTPRO):c.3255+83C>T	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241966	NM_030667.3(PTPRO):c.3255+226T>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253261	NM_030667.3(PTPRO):c.3255+320C>A	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1220804	NM_030667.3(PTPRO):c.3255+321A>C	PTPRO	Single nucleotide variant (intron variant)	not provided	GBenign

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