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Variants search result for Homo sapiens
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51 records found for search term Pnliprp1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155947120CV2262566single nucleotide variantNM_006229.4(PNLIPRP1):c.71A>G (p.Asp24Gly)not specified [RCV004130774]uncertain significance10116591792116591792Humanname
329354432CV2448169single nucleotide variantNM_006229.4(PNLIPRP1):c.71A>T (p.Asp24Val)not specified [RCV004263383]uncertain significance10116591792116591792Humanname
405652340CV3376509single nucleotide variantNM_006229.4(PNLIPRP1):c.76G>C (p.Gly26Arg)not specified [RCV004509719]uncertain significance10116591797116591797Humanname
407471861CV3463807single nucleotide variantNM_006229.4(PNLIPRP1):c.67G>A (p.Glu23Lys)not specified [RCV004662383]uncertain significance10116591788116591788Humanname
597743506CV3580630single nucleotide variantNM_006229.4(PNLIPRP1):c.76G>A (p.Gly26Arg)not specified [RCV004845082]uncertain significance10116591797116591797Humanname
8633508CV88723single nucleotide variantNM_006229.3(PNLIPRP1):c.600C>T (p.Phe200=)Malignant melanoma [RCV000068818]not provided10116597853116597853Humanname
156067921CV2193649single nucleotide variantNM_006229.4(PNLIPRP1):c.157G>A (p.Gly53Ser)not specified [RCV004074251]uncertain significance10116591878116591878Humanname
155924983CV2277222single nucleotide variantNM_006229.4(PNLIPRP1):c.269G>A (p.Arg90Gln)not specified [RCV004142849]uncertain significance10116592480116592480Humanname
401745975CV2678743single nucleotide variantNM_006229.4(PNLIPRP1):c.104G>A (p.Gly35Asp)not specified [RCV004292739]uncertain significance10116591825116591825Humanname
405652330CV3376504single nucleotide variantNM_006229.4(PNLIPRP1):c.164G>A (p.Arg55His)not specified [RCV004509714]uncertain significance10116591885116591885Humanname
407524368CV3463808single nucleotide variantNM_006229.4(PNLIPRP1):c.254T>C (p.Met85Thr)not specified [RCV004653553]likely benign10116592465116592465Humanname
156320226CV2197253single nucleotide variantNM_006229.4(PNLIPRP1):c.623G>A (p.Arg208Gln)not specified [RCV004079031]uncertain significance10116597876116597876Humanname
156213393CV2257369single nucleotide variantNM_006229.4(PNLIPRP1):c.665C>T (p.Thr222Met)not specified [RCV004125459]uncertain significance10116597918116597918Humanname
156319280CV2260813single nucleotide variantNM_006229.4(PNLIPRP1):c.546C>G (p.Ser182Arg)not specified [RCV004125724]uncertain significance10116596294116596294Humanname
156171491CV2293146single nucleotide variantNM_006229.4(PNLIPRP1):c.431G>T (p.Gly144Val)not specified [RCV004150666]uncertain significance10116594830116594830Humanname
156197563CV2334295single nucleotide variantNM_006229.4(PNLIPRP1):c.520G>C (p.Ala174Pro)not specified [RCV004188275]uncertain significance10116596268116596268Humanname
156205907CV2385263single nucleotide variantNM_006229.4(PNLIPRP1):c.820C>T (p.Arg274Trp)not specified [RCV004228504]uncertain significance10116600052116600052Humanname
329359380CV2436133single nucleotide variantNM_006229.4(PNLIPRP1):c.485C>G (p.Pro162Arg)not specified [RCV004249376]uncertain significance10116596233116596233Humanname
329377040CV2456860single nucleotide variantNM_006229.4(PNLIPRP1):c.325T>C (p.Cys109Arg)not specified [RCV004270822]uncertain significance10116592536116592536Humanname
401758518CV2694143single nucleotide variantNM_006229.4(PNLIPRP1):c.340G>A (p.Glu114Lys)not specified [RCV004302571]likely benign10116594739116594739Humanname
401864826CV2757213single nucleotide variantNM_006229.4(PNLIPRP1):c.487T>G (p.Ser163Ala)not specified [RCV004338812]uncertain significance10116596235116596235Humanname
401874103CV2772804single nucleotide variantNM_006229.4(PNLIPRP1):c.613G>A (p.Glu205Lys)not specified [RCV004357595]uncertain significance10116597866116597866Humanname
401882844CV2775124single nucleotide variantNM_006229.4(PNLIPRP1):c.998C>T (p.Ala333Val)not specified [RCV004346483]uncertain significance10116601136116601136Humanname
401876701CV2783035single nucleotide variantNM_006229.4(PNLIPRP1):c.470A>G (p.Glu157Gly)not specified [RCV004361816]uncertain significance10116596218116596218Humanname
401877133CV2790060single nucleotide variantNM_006229.4(PNLIPRP1):c.485C>T (p.Pro162Leu)not specified [RCV004364010]uncertain significance10116596233116596233Humanname
405652332CV3376505single nucleotide variantNM_006229.4(PNLIPRP1):c.306G>C (p.Glu102Asp)not specified [RCV004509715]uncertain significance10116592517116592517Humanname
405652334CV3376506single nucleotide variantNM_006229.4(PNLIPRP1):c.320A>G (p.Asp107Gly)not specified [RCV004509716]uncertain significance10116592531116592531Humanname
405652336CV3376507single nucleotide variantNM_006229.4(PNLIPRP1):c.484C>T (p.Pro162Ser)not specified [RCV004509717]uncertain significance10116596232116596232Humanname
405652338CV3376508single nucleotide variantNM_006229.4(PNLIPRP1):c.526G>A (p.Val176Met)not specified [RCV004509718]uncertain significance10116596274116596274Humanname
405652342CV3376510single nucleotide variantNM_006229.4(PNLIPRP1):c.815G>A (p.Gly272Glu)not specified [RCV004509720]uncertain significance10116600047116600047Humanname
405652344CV3376511single nucleotide variantNM_006229.4(PNLIPRP1):c.947C>T (p.Pro316Leu)not specified [RCV004509721]uncertain significance10116601085116601085Humanname
597743834CV3580628single nucleotide variantNM_006229.4(PNLIPRP1):c.877C>T (p.Leu293Phe)not specified [RCV004845080]uncertain significance10116600109116600109Humanname
597743654CV3580629single nucleotide variantNM_006229.4(PNLIPRP1):c.587T>C (p.Val196Ala)not specified [RCV004845081]uncertain significance10116597840116597840Humanname
597743511CV3580631single nucleotide variantNM_006229.4(PNLIPRP1):c.768G>T (p.Lys256Asn)not specified [RCV004845083]uncertain significance10116598120116598120Humanname
597743523CV3580633single nucleotide variantNM_006229.4(PNLIPRP1):c.795T>A (p.Asp265Glu)not specified [RCV004845085]uncertain significance10116598147116598147Humanname
598187312CV4003468single nucleotide variantNM_006229.4(PNLIPRP1):c.760G>A (p.Gly254Arg)not specified [RCV005395902]uncertain significance10116598112116598112Humanname
598187326CV4003470single nucleotide variantNM_006229.4(PNLIPRP1):c.888T>A (p.Asp296Glu)not specified [RCV005395904]uncertain significance10116600120116600120Humanname
598187337CV4003471single nucleotide variantNM_006229.4(PNLIPRP1):c.928G>C (p.Glu310Gln)not specified [RCV005395905]uncertain significance10116600160116600160Humanname
8633509CV88724single nucleotide variantNM_006229.3(PNLIPRP1):c.904C>T (p.Pro302Ser)Malignant melanoma [RCV000068819]not provided10116600136116600136Humanname
156226470CV2352746single nucleotide variantNM_006229.4(PNLIPRP1):c.1238T>C (p.Ile413Thr)not specified [RCV004198768]uncertain significance10116605451116605451Humanname
401758846CV2694310single nucleotide variantNM_006229.4(PNLIPRP1):c.1060G>A (p.Ala354Thr)not specified [RCV004304507]likely benign10116601198116601198Humanname
405652321CV3376500single nucleotide variantNM_006229.4(PNLIPRP1):c.1082C>A (p.Ser361Tyr)not specified [RCV004509710]uncertain significance10116604048116604048Humanname
405652324CV3376501single nucleotide variantNM_006229.4(PNLIPRP1):c.1118T>A (p.Ile373Asn)not specified [RCV004509711]uncertain significance10116604084116604084Humanname
405652326CV3376502single nucleotide variantNM_006229.4(PNLIPRP1):c.1131G>C (p.Leu377Phe)not specified [RCV004509712]uncertain significance10116604097116604097Humanname
405652328CV3376503single nucleotide variantNM_006229.4(PNLIPRP1):c.1294G>C (p.Val432Leu)not specified [RCV004509713]uncertain significance10116605507116605507Humanname
597743516CV3580632single nucleotide variantNM_006229.4(PNLIPRP1):c.1144G>A (p.Gly382Arg)not specified [RCV004845084]uncertain significance10116604110116604110Humanname
597743530CV3580634single nucleotide variantNM_006229.4(PNLIPRP1):c.1316T>C (p.Val439Ala)not specified [RCV004845086]uncertain significance10116605529116605529Humanname
598187297CV4003466single nucleotide variantNM_006229.4(PNLIPRP1):c.1006A>T (p.Thr336Ser)not specified [RCV005395900]uncertain significance10116601144116601144Humanname
598187305CV4003467single nucleotide variantNM_006229.4(PNLIPRP1):c.1066T>C (p.Trp356Arg)not specified [RCV005395901]uncertain significance10116604032116604032Humanname
598187320CV4003469single nucleotide variantNM_006229.4(PNLIPRP1):c.1265A>G (p.Asn422Ser)not specified [RCV005395903]uncertain significance10116605478116605478Humanname
8633510CV88725single nucleotide variantNM_006229.3(PNLIPRP1):c.1324G>A (p.Gly442Arg)Malignant melanoma [RCV000068820]not provided10116605537116605537Humanname