"GeneDx"[submitter] AND "GPD1L"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1182620	NC_000003.12:g.32106298G>A	GPD1L	Single nucleotide variant	not provided	GBenign
Select item 672822	NM_015141.3(GPD1L):c.-365G>A	GPD1L	Single nucleotide variant	not provided	GLikely benign
Select item 683540	NM_015141.3(GPD1L):c.-291G>A	GPD1L, LOC129936414	Single nucleotide variant	not provided	GBenign
Select item 1229730	NC_000003.12:g.32106485_32106502del	GPD1L, LOC129936414	Deletion	not provided	GBenign
Select item 671016	NM_015141.3(GPD1L):c.-227T>G	GPD1L, LOC129936414	Single nucleotide variant	not provided	GBenign
Select item 1259211	NM_015141.3(GPD1L):c.-119C>T	GPD1L, LOC129936414	Single nucleotide variant	not provided	GBenign
Select item 391851	NM_015141.4(GPD1L):c.-47C>G	GPD1L, LOC129936414	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 1307864	NM_015141.4(GPD1L):c.1A>G (p.Met1Val)	GPD1L, LOC129936414 (M1V)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 2662773	NM_015141.4(GPD1L):c.5C>T (p.Ala2Val)	GPD1L, LOC129936414 (A2V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 190765	NM_015141.4(GPD1L):c.8del (p.Ala3fs)	GPD1L, LOC129936414 (A3fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1260903	NM_015141.4(GPD1L):c.48-154_48-145del	GPD1L	Deletion (intron variant)	not provided	GBenign
Select item 674190	NM_015141.4(GPD1L):c.48-128G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 507174	NM_015141.4(GPD1L):c.48-6_48-3dup	GPD1L	Duplication (intron variant)	not specified	GLikely benign
Select item 190760	NM_015141.4(GPD1L):c.81T>C (p.Asn27=)	GPD1L	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 849673	NM_015141.4(GPD1L):c.119T>G (p.Met40Arg)	GPD1L (M40R)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 1878912	NM_015141.4(GPD1L):c.137C>G (p.Thr46Arg)	GPD1L (T46R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1311331	NM_015141.4(GPD1L):c.225_225+2del	GPD1L	Deletion (splice donor variant)	not provided	GUncertain significance
Select item 674299	NM_015141.4(GPD1L):c.225+175T>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258429	NM_015141.4(GPD1L):c.226-118_226-117insGACA	GPD1L	Insertion (intron variant)	not provided	GBenign
Select item 1230042	NM_015141.4(GPD1L):c.226-114G>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1212906	NM_015141.4(GPD1L):c.226-42G>C	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1310299	NM_015141.4(GPD1L):c.229G>T (p.Ala77Ser)	GPD1L (A77S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 787	NM_015141.4(GPD1L):c.247G>A (p.Glu83Lys)	GPD1L	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 560688	NM_015141.4(GPD1L):c.257A>G (p.Gln86Arg)	GPD1L (Q86R)	Single nucleotide variant (missense variant)	Brugada syndrome 2 +2 more	GUncertain significance
Select item 509377	NM_015141.4(GPD1L):c.336C>A (p.Pro112=)	GPD1L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 190761	NM_015141.4(GPD1L):c.366+8G>A	GPD1L	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 683541	NM_015141.4(GPD1L):c.367-317A>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248302	NM_015141.4(GPD1L):c.367-271G>C	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 671831	NM_015141.4(GPD1L):c.367-36G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250797	NM_015141.4(GPD1L):c.367-11C>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome 2 +1 more	GBenign/Likely benign
Select item 1245688	NM_015141.4(GPD1L):c.367-10A>T	GPD1L	Single nucleotide variant	not provided +1 more	GBenign/Likely benign
Select item 788	NM_015141.4(GPD1L):c.370A>G (p.Ile124Val)	GPD1L (I124V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 390828	NM_015141.4(GPD1L):c.384C>T (p.Pro128=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1052184	NM_015141.4(GPD1L):c.391C>A (p.Leu131Met)	GPD1L (L131M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 190762	NM_015141.4(GPD1L):c.396G>A (p.Lys132=)	GPD1L	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1736995	NM_015141.4(GPD1L):c.400A>T (p.Ile134Phe)	GPD1L (I134F)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GUncertain significance
Select item 260571	NM_015141.4(GPD1L):c.408C>T (p.Asp136=)	GPD1L	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 377931	NM_015141.4(GPD1L):c.445C>T (p.Leu149=)	GPD1L	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 463285	NM_015141.4(GPD1L):c.459C>T (p.Asn153=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 263656	NM_015141.4(GPD1L):c.465C>T (p.Ala155=)	GPD1L	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 452285	NM_015141.4(GPD1L):c.505G>A (p.Gly169Ser)	GPD1L (G169S)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GUncertain significance
Select item 1254826	NM_015141.4(GPD1L):c.505+292_505+319del	GPD1L	Deletion (intron variant)	not provided	GLikely benign
Select item 1195284	NM_015141.4(GPD1L):c.506-342G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1194580	NM_015141.4(GPD1L):c.506-290C>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 678494	NM_015141.4(GPD1L):c.506-234A>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 671832	NM_015141.4(GPD1L):c.506-171G>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 671833	NM_015141.4(GPD1L):c.506-124C>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 671834	NM_015141.4(GPD1L):c.506-108G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1219062	NM_015141.4(GPD1L):c.506-79C>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 180369	NM_015141.4(GPD1L):c.520G>A (p.Glu174Lys)	GPD1L (E174K)	Single nucleotide variant (missense variant)	Brugada syndrome +4 more	GConflicting classifications of pathogenicity
Select item 569836	NM_015141.4(GPD1L):c.547C>G (p.Leu183Val)	GPD1L (L183V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 190763	NM_015141.4(GPD1L):c.573C>G (p.Thr191=)	GPD1L	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 391283	NM_015141.4(GPD1L):c.618+17G>C	GPD1L	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 674020	NM_015141.4(GPD1L):c.618+23del	GPD1L	Deletion (intron variant)	not provided	GBenign
Select item 1238670	NM_015141.4(GPD1L):c.618+274G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 678496	NM_015141.4(GPD1L):c.619-245A>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291186	NM_015141.4(GPD1L):c.619-224C>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 671835	NM_015141.4(GPD1L):c.619-135G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 671836	NM_015141.4(GPD1L):c.619-46T>C	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1209495	NM_015141.4(GPD1L):c.619-28C>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1253073	NM_015141.4(GPD1L):c.619-12T>C	GPD1L	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 416016	NM_015141.4(GPD1L):c.619-9C>G	GPD1L	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 426646	NM_015141.4(GPD1L):c.652G>A (p.Gly218Ser)	GPD1L (G218S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 656217	NM_015141.4(GPD1L):c.658C>T (p.Arg220Cys)	GPD1L (R220C)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 190764	NM_015141.4(GPD1L):c.659G>A (p.Arg220His)	GPD1L (R220H)	Single nucleotide variant (missense variant)	not provided +4 more	GLikely benign
Select item 1005549	NM_015141.4(GPD1L):c.671A>G (p.Asn224Ser)	GPD1L (N224S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 682535	NM_015141.4(GPD1L):c.684C>T (p.Ala228=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome +2 more	GLikely benign
Select item 532104	NM_015141.4(GPD1L):c.685G>A (p.Val229Ile)	GPD1L (V229I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 190766	NM_015141.4(GPD1L):c.691C>T (p.Arg231Cys)	GPD1L (R231C)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 668231	NM_015141.4(GPD1L):c.774C>T (p.Cys258=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 452456	NM_015141.4(GPD1L):c.812G>A (p.Arg271Gln)	GPD1L (R271Q)	Single nucleotide variant (missense variant)	Brugada syndrome +2 more	GUncertain significance
Select item 241021	NM_015141.4(GPD1L):c.813G>T (p.Arg271=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome 2 +3 more	GBenign/Likely benign
Select item 789	NM_015141.4(GPD1L):c.817C>T (p.Arg273Cys)	GPD1L (R273C)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 390100	NM_015141.4(GPD1L):c.828C>T (p.Ala276=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GBenign/Likely benign
Select item 1306513	NM_015141.4(GPD1L):c.829G>A (p.Glu277Lys)	GPD1L (E277K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 463290	NM_015141.4(GPD1L):c.837C>T (p.Phe279=)	GPD1L	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 786	NM_015141.4(GPD1L):c.839C>T (p.Ala280Val)	GPD1L (A280V)	Single nucleotide variant (missense variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 2662442	NM_015141.4(GPD1L):c.842G>A (p.Arg281Lys)	GPD1L (R281K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 668883	NM_015141.4(GPD1L):c.852+20C>T	GPD1L	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 674021	NM_015141.4(GPD1L):c.853-148C>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 672397	NM_015141.4(GPD1L):c.853-147G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235431	NM_015141.4(GPD1L):c.853-88dup	GPD1L	Duplication (intron variant)	not provided	GBenign
Select item 1263922	NM_015141.4(GPD1L):c.853-88del	GPD1L	Deletion (intron variant)	not provided	GBenign
Select item 1266088	NM_015141.4(GPD1L):c.853-89A>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290095	NM_015141.4(GPD1L):c.853-88A>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241764	NM_015141.4(GPD1L):c.853-87del	GPD1L	Deletion (intron variant)	not provided	GBenign
Select item 1224144	NM_015141.4(GPD1L):c.853-87G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1214719	NM_015141.4(GPD1L):c.853-41T>G	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1209501	NM_015141.4(GPD1L):c.853-22T>C	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 344729	NM_015141.4(GPD1L):c.876G>A (p.Glu292=)	GPD1L	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 518875	NM_015141.4(GPD1L):c.897C>T (p.Leu299=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome +2 more	GLikely benign
Select item 519277	NM_015141.4(GPD1L):c.906G>A (p.Pro302=)	GPD1L	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1268199	NM_015141.4(GPD1L):c.957C>T (p.Asp319=)	GPD1L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 388490	NM_015141.4(GPD1L):c.959+7C>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome +2 more	GLikely benign
Select item 386094	NM_015141.4(GPD1L):c.959+11C>T	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome 2 +2 more	GLikely benign
Select item 1262567	NM_015141.4(GPD1L):c.959+16G>A	GPD1L	Single nucleotide variant (intron variant)	Brugada syndrome +1 more	GBenign
Select item 675874	NM_015141.4(GPD1L):c.959+71C>T	GPD1L	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 683542	NM_015141.4(GPD1L):c.960-291G>A	GPD1L	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 424505	NM_015141.4(GPD1L):c.976G>T (p.Ala326Ser)	GPD1L (A326S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 137491	NM_015141.4(GPD1L):c.981G>A (p.Val327=)	GPD1L	Single nucleotide variant (synonymous variant)	Brugada syndrome 2 +3 more	GBenign/Likely benign

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