PRKD1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59932	GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3	LOC130055392, LOC130055393 +780 more	Copy number gain	See cases	GPathogenic
Select item 155119	GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3	ABHD4, ACIN1 +814 more	Copy number gain	See cases	GPathogenic
Select item 155681	GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3	TRDC, TRDD1 +859 more	Copy number gain	See cases	GPathogenic
Select item 155306	GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	LOC126861920, LOC126861921 +3280 more	Copy number gain	See cases	GPathogenic
Select item 146230	GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	GSC, GSC-DT +3275 more	Copy number gain	See cases	GPathogenic
Select item 57745	GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1	LOC130055370, LOC130055371 +840 more	Copy number loss	See cases	GPathogenic
Select item 57750	GRCh38/hg38 14q11.2-21.1(chr14:23548960-41983402)x1	ADCY4, AKAP6 +399 more	Copy number loss	See cases	GPathogenic
Select item 2579199	GRCh38/hg38 14q12(chr14:28766690-29666306)x1	FOXG1, LINC01551 +12 more	Copy number loss	Rett syndrome, congenital variant	GPathogenic
Select item 154183	GRCh38/hg38 14q12-13.1(chr14:28803988-33234266)x1	AKAP6, AP4S1 +73 more	Copy number loss	See cases	GPathogenic
Select item 758729	NM_002742.3(PRKD1):c.2723G>A (p.Arg908His)	PRKD1 (R908H +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 720359	NM_002742.3(PRKD1):c.2718T>G (p.Gly906=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2644146	NM_002742.3(PRKD1):c.2672A>G (p.His891Arg)	PRKD1 (H803R +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784280	NM_002742.3(PRKD1):c.2657A>G (p.Asn886Ser)	PRKD1 (N894S +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition +1 more	GBenign
Select item 1698759	NM_002742.3(PRKD1):c.2626C>T (p.Gln876Ter)	PRKD1 (Q788* +2 more)	Single nucleotide variant (nonsense)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 3040503	NM_002742.3(PRKD1):c.2619A>G (p.Ala873=)	PRKD1	Single nucleotide variant (synonymous variant)	PRKD1-related condition	GLikely benign
Select item 2225888	NM_002742.3(PRKD1):c.2573G>A (p.Arg858His)	PRKD1 (R858H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 720962	NM_002742.3(PRKD1):c.2565C>T (p.Ile855=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3042646	NM_002742.3(PRKD1):c.2564T>A (p.Ile855Asn)	PRKD1 (I767N +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition	GLikely benign
Select item 2574529	NM_002742.3(PRKD1):c.2498C>A (p.Thr833Asn)	PRKD1 (T745N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 756313	NM_002742.3(PRKD1):c.2457G>A (p.Leu819=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2406579	NM_002742.3(PRKD1):c.2453A>G (p.Asn818Ser)	PRKD1 (N818S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1685036	NM_002742.3(PRKD1):c.2443C>G (p.Leu815Val)	PRKD1 (L727V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1327445	NM_002742.3(PRKD1):c.2435-14G>A	PRKD1	Single nucleotide variant (intron variant)	Congenital heart defects and ectodermal dysplasia	GBenign
Select item 445978	NM_002742.3(PRKD1):c.2422A>G (p.Ile808Val)	PRKD1 (I816V +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition +1 more	GBenign/Likely benign
Select item 3034504	NM_002742.3(PRKD1):c.2370C>T (p.His790=)	PRKD1	Single nucleotide variant (synonymous variant)	PRKD1-related condition	GLikely benign
Select item 745073	NM_002742.3(PRKD1):c.2335G>A (p.Gly779Ser)	PRKD1 (G779S +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 493141	NM_002742.3(PRKD1):c.2280C>T (p.Tyr760=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 998171	NM_002742.3(PRKD1):c.2219G>A (p.Arg740Gln)	PRKD1 (R652Q +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 746294	NM_002742.3(PRKD1):c.2208G>A (p.Glu736=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1327446	NM_002742.3(PRKD1):c.2202T>C (p.Ile734=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2644147	NM_002742.3(PRKD1):c.2195G>A (p.Arg732Gln)	PRKD1 (R644Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1712698	NM_002742.3(PRKD1):c.2173C>T (p.Leu725Phe)	PRKD1 (L637F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1327447	NM_002742.3(PRKD1):c.2167-12T>A	PRKD1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1327448	NM_002742.3(PRKD1):c.2166+39A>C	PRKD1	Single nucleotide variant (intron variant)	Congenital heart defects and ectodermal dysplasia	GBenign
Select item 2487513	NM_002742.3(PRKD1):c.2154T>G (p.Asp718Glu)	PRKD1 (D726E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1700150	NM_002742.3(PRKD1):c.2134G>A (p.Val712Met)	PRKD1 (V624M +2 more)	Single nucleotide variant (missense variant)	Neurodevelopmental delay	GLikely pathogenic
Select item 1032082	NM_002742.3(PRKD1):c.2068-11C>A	PRKD1	Single nucleotide variant (intron variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 2502023	NM_002742.3(PRKD1):c.2015C>T (p.Ser672Leu)	PRKD1 (S584L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 161599	NM_002742.3(PRKD1):c.1993G>A (p.Asp665Asn)	PRKD1 (D665N +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 791591	NM_002742.3(PRKD1):c.1953G>A (p.Thr651=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1032081	NM_002742.3(PRKD1):c.1947T>G (p.Phe649Leu)	PRKD1 (F649L +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 2446294	NM_002742.3(PRKD1):c.1923TGT[1] (p.Val643del)	PRKD1 (V555del +2 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2623856	NM_002742.3(PRKD1):c.1921G>A (p.Gly641Ser)	PRKD1 (G553S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1691270	NM_002742.3(PRKD1):c.1905+2T>A	PRKD1	Single nucleotide variant (splice donor variant)	Congenital heart defects and ectodermal dysplasia	GLikely pathogenic
Select item 2331156	NM_002742.3(PRKD1):c.1897A>G (p.Ile633Val)	PRKD1 (I633V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2205819	NM_002742.3(PRKD1):c.1882C>T (p.Arg628Cys)	PRKD1 (R540C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1805098	NM_002742.3(PRKD1):c.1874G>T (p.Ser625Ile)	PRKD1 (S537I +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 203494	NM_002742.3(PRKD1):c.1852C>T (p.Arg618Ter)	PRKD1 (R618* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 3055507	NM_002742.3(PRKD1):c.1808G>T (p.Arg603Leu)	PRKD1 (R515L +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition	GUncertain significance
Select item 1934696	NM_002742.3(PRKD1):c.1808G>A (p.Arg603His)	PRKD1 (R515H +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia +1 more	GConflicting classifications of pathogenicity
Select item 2572890	NM_002742.3(PRKD1):c.1792T>G (p.Tyr598Asp)	PRKD1 (Y510D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 754461	NM_002742.3(PRKD1):c.1776A>G (p.Gly592=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 375740	NM_002742.3(PRKD1):c.1774G>A (p.Gly592Arg)	PRKD1 (G592R +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GPathogenic
Select item 1804122	NM_002742.3(PRKD1):c.1754C>T (p.Pro585Leu)	PRKD1 (P497L +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GBenign
Select item 2644148	NM_002742.3(PRKD1):c.1651G>A (p.Gly551Ser)	PRKD1 (G463S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2376754	NM_002742.3(PRKD1):c.1648G>A (p.Val550Met)	PRKD1 (V462M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2628732	NM_002742.3(PRKD1):c.1633C>T (p.Pro545Ser)	PRKD1 (P457S +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition	GUncertain significance
Select item 1085109	NM_002742.3(PRKD1):c.1627G>A (p.Val543Ile)	PRKD1 (V455I +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3052110	NM_002742.3(PRKD1):c.1626C>T (p.Pro542=)	PRKD1	Single nucleotide variant (synonymous variant)	PRKD1-related condition	GLikely benign
Select item 2336433	NM_002742.3(PRKD1):c.1609C>A (p.Gln537Lys)	PRKD1 (Q449K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2435246	NM_002742.3(PRKD1):c.1585G>A (p.Ala529Thr)	PRKD1 (A441T +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 2627323	NM_002742.3(PRKD1):c.1570G>A (p.Val524Ile)	PRKD1 (V436I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398261	NM_002742.3(PRKD1):c.1487C>T (p.Thr496Met)	PRKD1 (T408M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1122960	NM_002742.3(PRKD1):c.1477G>A (p.Glu493Lys)	PRKD1 (E405K +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 931739	NM_002742.3(PRKD1):c.1456G>A (p.Gly486Arg)	PRKD1 (G486R +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia +1 more	GUncertain significance
Select item 732997	NM_002742.3(PRKD1):c.1441G>A (p.Ala481Thr)	PRKD1 (A481T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2364745	NM_002742.3(PRKD1):c.1438T>C (p.Ser480Pro)	PRKD1 (S480P +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 735173	NM_002742.3(PRKD1):c.1420C>T (p.Leu474=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3052083	NM_002742.3(PRKD1):c.1393-10del	PRKD1	Deletion (intron variant)	PRKD1-related condition	GLikely benign
Select item 788800	NM_002742.3(PRKD1):c.1392+6A>G	PRKD1	Single nucleotide variant (intron variant)	PRKD1-related condition +1 more	GBenign/Likely benign
Select item 788801	NM_002742.3(PRKD1):c.1356C>T (p.Thr452=)	PRKD1	Single nucleotide variant (synonymous variant)	PRKD1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1032079	NM_002742.3(PRKD1):c.1322G>A (p.Arg441Gln)	PRKD1 (R441Q +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 803014	NM_002742.3(PRKD1):c.1316G>A (p.Arg439Gln)	PRKD1 (R351Q +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GLikely pathogenic
Select item 781270	NM_002742.3(PRKD1):c.1315-8T>C	PRKD1	Single nucleotide variant (intron variant)	PRKD1-related condition +1 more	GBenign
Select item 2479900	NM_002742.3(PRKD1):c.1304A>G (p.Lys435Arg)	PRKD1 (K443R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209369	NM_002742.3(PRKD1):c.1284G>T (p.Trp428Cys)	PRKD1 (W340C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2354379	NM_002742.3(PRKD1):c.1270A>G (p.Met424Val)	PRKD1 (M432V +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1700921	NM_002742.3(PRKD1):c.1213C>G (p.Pro405Ala)	PRKD1 (P317A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 768644	NM_002742.3(PRKD1):c.1191-6C>T	PRKD1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2386150	NM_002742.3(PRKD1):c.1168G>A (p.Glu390Lys)	PRKD1 (E390K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 732998	NM_002742.3(PRKD1):c.1140C>T (p.Gly380=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2395846	NM_002742.3(PRKD1):c.1128G>T (p.Gln376His)	PRKD1 (Q384H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2582918	NM_002742.3(PRKD1):c.1114A>G (p.Met372Val)	PRKD1 (M284V +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2388016	NM_002742.3(PRKD1):c.1088C>T (p.Ala363Val)	PRKD1 (A371V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469184	NM_002742.3(PRKD1):c.1080G>C (p.Met360Ile)	PRKD1 (M360I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2435244	NM_002742.3(PRKD1):c.1061G>A (p.Ser354Asn)	PRKD1 (S266N +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 731412	NM_002742.3(PRKD1):c.1021A>C (p.Met341Leu)	PRKD1 (M341L +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition +1 more	GBenign/Likely benign
Select item 2285404	NM_002742.3(PRKD1):c.1009T>C (p.Ser337Pro)	PRKD1 (S249P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 735588	NM_002742.3(PRKD1):c.960C>T (p.Cys320=)	PRKD1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3044767	NM_002742.3(PRKD1):c.942G>A (p.Pro314=)	PRKD1	Single nucleotide variant (synonymous variant)	PRKD1-related condition	GBenign
Select item 1685037	NM_002742.3(PRKD1):c.922T>G (p.Cys308Gly)	PRKD1 (C220G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786246	NM_002742.3(PRKD1):c.908-7G>A	PRKD1	Single nucleotide variant (intron variant)	PRKD1-related condition +1 more	GBenign/Likely benign
Select item 2370717	NM_002742.3(PRKD1):c.905A>G (p.Lys302Arg)	PRKD1 (K214R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 375741	NM_002742.3(PRKD1):c.896T>G (p.Leu299Trp)	PRKD1 (L299W +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GPathogenic
Select item 1805316	NM_002742.3(PRKD1):c.815C>T (p.Thr272Ile)	PRKD1 (T184I +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia	GUncertain significance
Select item 2631720	NM_002742.3(PRKD1):c.802A>T (p.Lys268Ter)	PRKD1 (K180* +2 more)	Single nucleotide variant (nonsense)	PRKD1-related condition	GUncertain significance
Select item 2634897	NM_002742.3(PRKD1):c.754T>C (p.Tyr252His)	PRKD1 (Y164H +2 more)	Single nucleotide variant (missense variant)	PRKD1-related condition	GUncertain significance
Select item 1206051	NM_002742.3(PRKD1):c.719T>G (p.Phe240Cys)	PRKD1 (F152C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545993	NM_002742.3(PRKD1):c.716C>T (p.Ser239Leu)	PRKD1 (S151L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282481	NM_002742.3(PRKD1):c.689C>T (p.Pro230Leu)	PRKD1 (P134L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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