"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PDP1"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2142627	NM_018444.4(PDP1):c.12A>G (p.Pro4=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1478331	NM_018444.4(PDP1):c.21G>C (p.Leu7=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2180244	NM_018444.4(PDP1):c.30T>C (p.Pro10=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2071700	NM_018444.4(PDP1):c.56G>C (p.Arg19Thr)	PDP1 (R19T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1576342	NM_018444.4(PDP1):c.57G>A (p.Arg19=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 511583	NM_018444.4(PDP1):c.87C>T (p.His29=)	PDP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2070346	NM_018444.4(PDP1):c.110C>T (p.Ser37Leu)	PDP1 (S37L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2054458	NM_018444.4(PDP1):c.111G>A (p.Ser37=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1934172	NM_018444.4(PDP1):c.111G>T (p.Ser37=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1998824	NM_018444.4(PDP1):c.123G>T (p.Gln41His)	PDP1 (Q66H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 214969	NM_018444.4(PDP1):c.128G>A (p.Arg43Gln)	PDP1 (R43Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1103750	NM_018444.4(PDP1):c.154T>C (p.Tyr52His)	PDP1 (Y52H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 762458	NM_018444.4(PDP1):c.171G>A (p.Arg57=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1525448	NM_018444.4(PDP1):c.202G>A (p.Gly68Arg)	PDP1 (G93R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1441866	NM_018444.4(PDP1):c.214G>T (p.Ala72Ser)	PDP1 (A72S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1370920	NM_018444.4(PDP1):c.247C>A (p.Pro83Thr)	PDP1 (P108T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2175773	NM_018444.4(PDP1):c.257A>G (p.Asn86Ser)	PDP1 (N111S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 515992	NM_018444.4(PDP1):c.261C>T (p.Ser87=)	PDP1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 853847	NM_018444.4(PDP1):c.263T>C (p.Ile88Thr)	PDP1 (I88T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1090200	NM_018444.4(PDP1):c.297A>C (p.Pro99=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2195439	NM_018444.4(PDP1):c.306C>T (p.Asp102=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2148274	NM_018444.4(PDP1):c.307G>A (p.Gly103Ser)	PDP1 (G103S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1671419	NM_018444.4(PDP1):c.351G>T (p.Leu117=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2166335	NM_018444.4(PDP1):c.354T>C (p.Pro118=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1424404	NM_018444.4(PDP1):c.362C>T (p.Ala121Val)	PDP1 (A121V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2162554	NM_018444.4(PDP1):c.368T>C (p.Ile123Thr)	PDP1 (I123T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1447615	NM_018444.4(PDP1):c.377G>A (p.Arg126Gln)	PDP1 (R151Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 516461	NM_018444.4(PDP1):c.418T>C (p.Leu140=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2167131	NM_018444.4(PDP1):c.444T>C (p.Gly148=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2800897	NM_018444.4(PDP1):c.456C>T (p.Ser152=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1486444	NM_018444.4(PDP1):c.457C>T (p.Gln153Ter)	PDP1 (Q153* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1989555	NM_018444.4(PDP1):c.477C>T (p.Leu159=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1627169	NM_018444.4(PDP1):c.483T>C (p.Tyr161=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2028085	NM_018444.4(PDP1):c.498T>G (p.Ser166=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2740031	NM_018444.4(PDP1):c.510T>C (p.His170=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1406005	NM_018444.4(PDP1):c.515C>T (p.Thr172Ile)	PDP1 (T172I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 363942	NM_018444.4(PDP1):c.546C>T (p.Ser182=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2078705	NM_018444.4(PDP1):c.550C>T (p.Arg184Trp)	PDP1 (R209W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1897127	NM_018444.4(PDP1):c.555A>G (p.Ala185=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2778049	NM_018444.4(PDP1):c.557T>A (p.Leu186Gln)	PDP1 (L186Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1981510	NM_018444.4(PDP1):c.597C>T (p.Tyr199=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1464519	NM_018444.4(PDP1):c.600T>A (p.Phe200Leu)	PDP1 (F225L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946326	NM_018444.4(PDP1):c.618A>G (p.Lys206=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2049175	NM_018444.4(PDP1):c.627dup (p.Asn210Ter)	PDP1 (N210* +1 more)	Duplication (nonsense)	not provided	GUncertain significance
Select item 2044518	NM_018444.4(PDP1):c.651A>G (p.Gln217=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1085315	NM_018444.4(PDP1):c.654G>A (p.Glu218=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2134689	NM_018444.4(PDP1):c.657T>C (p.Leu219=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 742858	NM_018444.4(PDP1):c.681G>A (p.Ser227=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2198387	NM_018444.4(PDP1):c.689T>C (p.Ile230Thr)	PDP1 (I230T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2161676	NM_018444.4(PDP1):c.690T>C (p.Ile230=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 363943	NM_018444.4(PDP1):c.717C>G (p.Ala239=)	PDP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1713816	NM_018444.4(PDP1):c.727C>T (p.Leu243Phe)	PDP1 (L243F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1935268	NM_018444.4(PDP1):c.753G>A (p.Ala251=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1489443	NM_018444.4(PDP1):c.803C>T (p.Ala268Val)	PDP1 (A268V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2051176	NM_018444.4(PDP1):c.831C>T (p.Ala277=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 750269	NM_018444.4(PDP1):c.855T>C (p.His285=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 654429	NM_018444.4(PDP1):c.870C>T (p.Gly290=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2010062	NM_018444.4(PDP1):c.871G>T (p.Asp291Tyr)	PDP1 (D291Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1930101	NM_018444.4(PDP1):c.897G>A (p.Gln299=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 138679	NM_018444.4(PDP1):c.906C>T (p.Asp302=)	PDP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 732239	NM_018444.4(PDP1):c.909C>T (p.Gly303=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1019550	NM_018444.4(PDP1):c.926C>T (p.Thr309Met)	PDP1 (T309M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2001166	NM_018444.4(PDP1):c.935A>C (p.Asn312Thr)	PDP1 (N337T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978948	NM_018444.4(PDP1):c.967G>A (p.Glu323Lys)	PDP1 (E348K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1897143	NM_018444.4(PDP1):c.970C>T (p.Arg324Trp)	PDP1 (R324W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1618475	NM_018444.4(PDP1):c.972G>C (p.Arg324=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1568803	NM_018444.4(PDP1):c.990A>G (p.Pro330=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 744266	NM_018444.4(PDP1):c.993G>A (p.Lys331=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 794036	NM_018444.4(PDP1):c.1011C>T (p.Val337=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 734511	NM_018444.4(PDP1):c.1029G>C (p.Leu343=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2909170	NM_018444.4(PDP1):c.1104G>A (p.Val368=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2190764	NM_018444.4(PDP1):c.1119A>G (p.Pro373=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2190521	NM_018444.4(PDP1):c.1130A>G (p.Asn377Ser)	PDP1 (N402S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1379291	NM_018444.4(PDP1):c.1136A>G (p.Asn379Ser)	PDP1 (N379S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1717594	NM_018444.4(PDP1):c.1160C>G (p.Pro387Arg)	PDP1 (P387R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2055079	NM_018444.4(PDP1):c.1214G>A (p.Arg405Gln)	PDP1 (R430Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1411625	NM_018444.4(PDP1):c.1217T>A (p.Leu406Ter)	PDP1 (L406* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1563937	NM_018444.4(PDP1):c.1233G>A (p.Lys411=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1392455	NM_018444.4(PDP1):c.1268C>A (p.Thr423Asn)	PDP1 (T423N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1044534	NM_018444.4(PDP1):c.1274A>G (p.His425Arg)	PDP1 (H425R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1007261	NM_018444.4(PDP1):c.1281G>C (p.Gln427His)	PDP1 (Q427H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2122695	NM_018444.4(PDP1):c.1283A>G (p.Asp428Gly)	PDP1 (D428G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1004779	NM_018444.4(PDP1):c.1284T>A (p.Asp428Glu)	PDP1 (D428E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2060382	NM_018444.4(PDP1):c.1321C>A (p.His441Asn)	PDP1 (H466N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 736522	NM_018444.4(PDP1):c.1341T>G (p.Ala447=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2416190	NM_018444.4(PDP1):c.1342G>A (p.Val448Ile)	PDP1 (V448I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2122097	NM_018444.4(PDP1):c.1346G>A (p.Gly449Asp)	PDP1 (G449D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 953162	NM_018444.4(PDP1):c.1355A>G (p.Lys452Arg)	PDP1 (K477R +1 more)	Single nucleotide variant (missense variant)	Pyruvate dehydrogenase phosphatase deficiency +1 more	GUncertain significance
Select item 2856205	NM_018444.4(PDP1):c.1398A>G (p.Arg466=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1444187	NM_018444.4(PDP1):c.1413G>A (p.Ser471=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1630903	NM_018444.4(PDP1):c.1416A>G (p.Val472=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 138680	NM_018444.4(PDP1):c.1431C>T (p.Asn477=)	PDP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1987313	NM_018444.4(PDP1):c.1432G>A (p.Ala478Thr)	PDP1 (A503T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 511369	NM_018444.4(PDP1):c.1434A>G (p.Ala478=)	PDP1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1619060	NM_018444.4(PDP1):c.1446C>T (p.Leu482=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1424256	NM_018444.4(PDP1):c.1450C>G (p.Arg484Gly)	PDP1 (R484G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1589360	NM_018444.4(PDP1):c.1455C>T (p.His485=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 842881	NM_018444.4(PDP1):c.1456G>A (p.Ala486Thr)	PDP1 (A486T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2024290	NM_018444.4(PDP1):c.1500C>T (p.Leu500=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2005334	NM_018444.4(PDP1):c.1521T>C (p.Pro507=)	PDP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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