"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "PNPLA6" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 330504	NM_020533.3(MCOLN1):c.1360-13G>A	MCOLN1, PNPLA6	Single nucleotide variant (intron variant)	Spastic Paraplegia, Recessive +2 more	GBenign/Likely benign
Select item 894185	NM_020533.3(MCOLN1):c.1458C>A (p.Arg486=)	MCOLN1, PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39 +1 more	GConflicting classifications of pathogenicity
Select item 240695	NM_006702.5(PNPLA6):c.2T>C (p.Met1Thr)	LOC130063377, PNPLA6 (M1T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1621621	NC_000019.10:g.7535556G>A	PNPLA6, LOC130063377	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2768502	NC_000019.10:g.7535557G>A	LOC130063377, PNPLA6 (A3T)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2018933	NC_000019.10:g.7535562G>A	LOC130063377, PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 843409	NC_000019.10:g.7535563_7535564delinsGG	LOC130063377, PNPLA6 (L5G)	Indel (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 935764	NC_000019.10:g.7535564T>A	LOC130063377, PNPLA6 (L5Q)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1716898	NC_000019.10:g.7535573G>A	LOC130063377, PNPLA6 (G8E)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2202447	NC_000019.10:g.7535576T>C	LOC130063377, PNPLA6 (M9T)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1564071	NC_000019.10:g.7535588G>C	PNPLA6, LOC130063377	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2820861	NC_000019.10:g.7535591C>A	LOC130063377, PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1583042	NC_000019.10:g.7535591C>T	LOC130063377, PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39 +1 more	GLikely benign
Select item 2708945	NC_000019.10:g.7535595G>A	LOC130063377, PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1630158	NM_001166114.2(PNPLA6):c.130C>T (p.Pro44Ser)	PNPLA6 (P44S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 893384	NM_001166114.2(PNPLA6):c.131C>T (p.Pro44Leu)	PNPLA6 (P44L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2104031	NM_001166114.2(PNPLA6):c.136G>T (p.Val46Phe)	PNPLA6 (V46F +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2128472	NM_001166114.2(PNPLA6):c.138C>T (p.Val46=)	PNPLA6	Single nucleotide variant (synonymous variant +1 more)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1544164	NM_001166114.2(PNPLA6):c.139C>T (p.Pro47Ser)	PNPLA6 (P47S +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2414035	NM_001166114.2(PNPLA6):c.140C>T (p.Pro47Leu)	PNPLA6 (P47L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary spastic paraplegia 39	GLikely benign
Select item 944016	NM_001166114.2(PNPLA6):c.148C>T (p.Leu50Phe)	PNPLA6 (L50F +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1944899	NM_001166114.2(PNPLA6):c.154G>A (p.Val52Met)	PNPLA6 (V13M +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2709725	NM_001166114.2(PNPLA6):c.156G>T (p.Val52=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1052610	NM_001166114.2(PNPLA6):c.163_186dup (p.Gly55_Val62dup)	PNPLA6	Duplication (inframe_insertion)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 240702	NM_001166114.2(PNPLA6):c.162C>T (p.Ile54=)	PNPLA6	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2064966	NM_001166114.2(PNPLA6):c.166G>T (p.Ala56Ser)	PNPLA6 (A17S +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 937022	NM_001166114.2(PNPLA6):c.169G>C (p.Gly57Arg)	PNPLA6 (G66R +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 469623	NM_001166114.2(PNPLA6):c.171A>C (p.Gly57=)	PNPLA6	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 281419	NM_001166114.2(PNPLA6):c.173T>C (p.Val58Ala)	MCOLN1, PNPLA6 (V19A +2 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 240703	NM_001166114.2(PNPLA6):c.181G>C (p.Val61Leu)	MCOLN1, PNPLA6 (V22L +2 more)	Single nucleotide variant (missense variant)	Mucolipidosis type IV +8 more	GBenign/Likely benign
Select item 330512	NM_001166114.2(PNPLA6):c.183G>A (p.Val61=)	MCOLN1, PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39 +5 more	GBenign/Likely benign
Select item 1911706	NM_001166114.2(PNPLA6):c.188C>T (p.Thr63Met)	PNPLA6 (T72M +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1997938	NM_001166114.2(PNPLA6):c.192C>G (p.Ala64=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2132537	NM_001166114.2(PNPLA6):c.193G>A (p.Val65Met)	PNPLA6 (V74M +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1345601	NM_001166114.2(PNPLA6):c.197T>G (p.Leu66Arg)	PNPLA6 (L27R +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 938224	NM_001166114.2(PNPLA6):c.202C>T (p.Leu68Phe)	PNPLA6 (L29F +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2187080	NM_001166114.2(PNPLA6):c.207G>A (p.Leu69=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2759232	NM_001166114.2(PNPLA6):c.215G>A (p.Arg72Gln)	PNPLA6 (R72Q +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1533140	NM_001166114.2(PNPLA6):c.216G>C (p.Arg72=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1397570	NM_001166114.2(PNPLA6):c.217A>G (p.Arg73Gly)	PNPLA6 (R82G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2148912	NM_001166114.2(PNPLA6):c.219G>C (p.Arg73Ser)	PNPLA6 (R82S +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1132688	NM_001166114.2(PNPLA6):c.220C>T (p.Leu74=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2130511	NM_001166114.2(PNPLA6):c.224G>A (p.Arg75Gln)	PNPLA6 (R84Q +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 392043	NM_001166114.2(PNPLA6):c.225A>G (p.Arg75=)	PNPLA6	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1046252	NM_001166114.2(PNPLA6):c.226G>A (p.Val76Met)	PNPLA6 (V37M +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 509801	NM_001166114.2(PNPLA6):c.232+14G>A	PNPLA6	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2048202	NM_001166114.2(PNPLA6):c.232+15G>A	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2080412	NM_001166114.2(PNPLA6):c.232+16G>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2765496	NM_001166114.2(PNPLA6):c.233-16C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1945588	NM_001166114.2(PNPLA6):c.233-16C>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1596757	NM_001166114.2(PNPLA6):c.233-15C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1590041	NM_001166114.2(PNPLA6):c.233-13C>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2102772	NM_001166114.2(PNPLA6):c.233-11C>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 240690	NM_001166114.2(PNPLA6):c.233-8A>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1516269	NM_001166114.2(PNPLA6):c.238C>T (p.Pro80Ser)	PNPLA6 (P89S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1152533	NM_001166114.2(PNPLA6):c.240A>C (p.Pro80=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1132736	NM_001166114.2(PNPLA6):c.246G>A (p.Pro82=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2136970	NM_001166114.2(PNPLA6):c.252C>A (p.Gly84=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 706194	NM_001166114.2(PNPLA6):c.261T>C (p.Tyr87=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2811257	NM_001166114.2(PNPLA6):c.264G>A (p.Arg88=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 936817	NM_001166114.2(PNPLA6):c.266del (p.Phe89fs)	PNPLA6 (F98fs +2 more)	Deletion (frameshift variant)	Hereditary spastic paraplegia 39	GPathogenic
Select item 1545809	NM_001166114.2(PNPLA6):c.267C>T (p.Phe89=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1091102	NM_001166114.2(PNPLA6):c.288C>T (p.Leu96=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39 +1 more	GLikely benign
Select item 1146752	NM_001166114.2(PNPLA6):c.294T>C (p.Tyr98=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 894217	NM_001166114.2(PNPLA6):c.306T>A (p.Ile102=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GConflicting classifications of pathogenicity
Select item 2714396	NM_001166114.2(PNPLA6):c.315+1G>T	PNPLA6	Single nucleotide variant (splice donor variant)	Hereditary spastic paraplegia 39	GLikely pathogenic
Select item 1106906	NM_001166114.2(PNPLA6):c.315+8C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2182833	NM_001166114.2(PNPLA6):c.315+13C>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 330513	NM_001166114.2(PNPLA6):c.315+13C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39 +1 more	GConflicting classifications of pathogenicity
Select item 1598507	NM_001166114.2(PNPLA6):c.315+16C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1634624	NM_001166114.2(PNPLA6):c.315+19G>A	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1568577	NM_001166114.2(PNPLA6):c.315+19G>C	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1170661	NM_001166114.2(PNPLA6):c.316-18C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GBenign
Select item 2054241	NM_001166114.2(PNPLA6):c.316-17C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2148638	NM_001166114.2(PNPLA6):c.316-16G>A	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2017361	NM_001166114.2(PNPLA6):c.316-14C>T	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1457125	NM_001166114.2(PNPLA6):c.316-10_316-7dup	PNPLA6	Duplication (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1576457	NM_001166114.2(PNPLA6):c.316-12_316-11delinsAT	PNPLA6	Indel (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 872466	NM_001166114.2(PNPLA6):c.316-2A>T	PNPLA6	Single nucleotide variant (splice acceptor variant)	Ataxia-hypogonadism-choroidal dystrophy syndrome +3 more	GPathogenic
Select item 1113605	NM_001166114.2(PNPLA6):c.318G>A (p.Val106=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1674229	NM_001166114.2(PNPLA6):c.327C>A (p.Ser109=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2012465	NM_001166114.2(PNPLA6):c.331TCC[1] (p.Ser112del)	PNPLA6 (S112del +2 more)	Microsatellite (inframe_deletion)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1388352	NM_001166114.2(PNPLA6):c.334T>A (p.Ser112Thr)	PNPLA6 (S121T +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2709334	NM_001166114.2(PNPLA6):c.339C>T (p.Leu113=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1004981	NM_001166114.2(PNPLA6):c.347C>T (p.Thr116Ile)	PNPLA6 (T116I +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1130869	NM_001166114.2(PNPLA6):c.357C>T (p.Ser119=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 969903	NM_001166114.2(PNPLA6):c.358G>A (p.Ala120Thr)	PNPLA6 (A129T +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2199497	NM_001166114.2(PNPLA6):c.365C>G (p.Ser122Cys)	PNPLA6 (S83C +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 2911959	NM_001166114.2(PNPLA6):c.366C>T (p.Ser122=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1024073	NM_001166114.2(PNPLA6):c.367C>A (p.Arg123=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1143577	NM_001166114.2(PNPLA6):c.372A>G (p.Pro124=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2008042	NM_001166114.2(PNPLA6):c.376A>C (p.Met126Leu)	PNPLA6 (M87L +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1585282	NM_001166114.2(PNPLA6):c.381G>A (p.Arg127=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2101068	NM_001166114.2(PNPLA6):c.384G>A (p.Lys128=)	PNPLA6	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2078280	NM_001166114.2(PNPLA6):c.401A>G (p.Asn134Ser)	PNPLA6 (N95S +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1517236	NM_001166114.2(PNPLA6):c.401A>C (p.Asn134Thr)	PNPLA6 (N95T +2 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 39	GUncertain significance
Select item 1956913	NM_001166114.2(PNPLA6):c.413+1G>A	PNPLA6	Single nucleotide variant (splice donor variant)	Hereditary spastic paraplegia 39	GLikely pathogenic
Select item 1148528	NM_001166114.2(PNPLA6):c.413+8T>A	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 1919172	NM_001166114.2(PNPLA6):c.413+11G>C	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign
Select item 2885293	NM_001166114.2(PNPLA6):c.413+13T>G	PNPLA6	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 39	GLikely benign

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