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38 records found for search term Parl
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155645470CV1708945single nucleotide variantNM_018622.7(PARL):c.511+4771C>TLeprosy, susceptibility to, 1 [RCV002291821]uncertain risk allele3183857982183857982Human2name
155645470CV1708945single nucleotide variantNM_018622.7(PARL):c.511+4771C>TLeprosy, susceptibility to, 1 [RCV002291821]uncertain risk allele3183857982183857983Human2name
15191194CV763751single nucleotide variantNM_018622.7(PARL):c.30C>T (p.Gly10=)not provided [RCV000932734]likely benign3183884817183884817Humanname
15200620CV720313single nucleotide variantNM_018622.7(PARL):c.123C>T (p.Arg41=)not provided [RCV000890962]likely benign3183884724183884724Humanname
408381199CV3501425single nucleotide variantNM_018622.7(PARL):c.813A>G (p.Gly271=)not provided [RCV004727514]uncertain significance3183840585183840585Humanname
598260002CV4002041single nucleotide variantNM_018622.7(PARL):c.83A>C (p.Glu28Ala)not specified [RCV005386598]uncertain significance3183884764183884764Humanname
10448649CV214751single nucleotide variantNM_018622.7(PARL):c.230G>A (p.Ser77Asn)not provided [RCV000202343]uncertain significance3183867956183867956Humanname
156286793CV2232998single nucleotide variantNM_018622.7(PARL):c.275C>T (p.Pro92Leu)not specified [RCV004103368]uncertain significance3183867911183867911Humanname
329384397CV2435052single nucleotide variantNM_018622.7(PARL):c.154G>A (p.Gly52Arg)not specified [RCV004252702]uncertain significance3183868032183868032Humanname
405772451CV3364365single nucleotide variantNM_018622.7(PARL):c.122G>T (p.Arg41Leu)not specified [RCV004502550]uncertain significance3183884725183884725Humanname
405772457CV3364366single nucleotide variantNM_018622.7(PARL):c.172A>G (p.Arg58Gly)not specified [RCV004502551]uncertain significance3183868014183868014Humanname
405772464CV3364367single nucleotide variantNM_018622.7(PARL):c.227G>C (p.Arg76Thr)not specified [RCV004502552]uncertain significance3183867959183867959Humanname
405772470CV3364368single nucleotide variantNM_018622.7(PARL):c.290G>A (p.Ser97Asn)not specified [RCV004502553]uncertain significance3183867896183867896Humanname
407518249CV3466567single nucleotide variantNM_018622.7(PARL):c.281C>T (p.Pro94Leu)not specified [RCV004650938]uncertain significance3183867905183867905Humanname
597658039CV3571492single nucleotide variantNM_018622.7(PARL):c.211G>T (p.Gly71Cys)not specified [RCV004827734]uncertain significance3183867975183867975Humanname
597719015CV3571493single nucleotide variantNM_018622.7(PARL):c.127T>A (p.Phe43Ile)not specified [RCV004841699]uncertain significance3183868059183868059Humanname
598259986CV4002038single nucleotide variantNM_018622.7(PARL):c.274C>T (p.Pro92Ser)not specified [RCV005386595]uncertain significance3183867912183867912Humanname
156343394CV2232704single nucleotide variantNM_018622.7(PARL):c.593C>T (p.Ser198Leu)not specified [RCV004101363]uncertain significance3183844245183844245Humanname
156176442CV2278287single nucleotide variantNM_018622.7(PARL):c.568C>T (p.Arg190Trp)not specified [RCV004147594]uncertain significance3183844270183844270Humanname
156171974CV2380762single nucleotide variantNM_018622.7(PARL):c.923C>T (p.Ala308Val)not specified [RCV004218328]uncertain significance3183833731183833731Humanname
329362046CV2456681single nucleotide variantNM_018622.7(PARL):c.887T>G (p.Leu296Arg)not specified [RCV004277857]uncertain significance3183833767183833767Humanname
405772829CV3364369single nucleotide variantNM_018622.7(PARL):c.485T>C (p.Leu162Pro)not specified [RCV004502554]uncertain significance3183862779183862779Humanname
405772481CV3364370single nucleotide variantNM_018622.7(PARL):c.892A>G (p.Ile298Val)not specified [RCV004502555]uncertain significance3183833762183833762Humanname
405772487CV3364371single nucleotide variantNM_018622.7(PARL):c.986T>G (p.Phe329Cys)not specified [RCV004502556]uncertain significance3183833534183833534Humanname
407518252CV3466568single nucleotide variantNM_018622.7(PARL):c.332G>A (p.Cys111Tyr)not specified [RCV004650939]uncertain significance3183866755183866755Humanname
407518255CV3466569single nucleotide variantNM_018622.7(PARL):c.450C>A (p.Asp150Glu)not specified [RCV004650940]uncertain significance3183866637183866637Humanname
407518258CV3466570single nucleotide variantNM_018622.7(PARL):c.820C>T (p.Leu274Phe)not specified [RCV004650941]uncertain significance3183840578183840578Humanname
597718998CV3571489single nucleotide variantNM_018622.7(PARL):c.895A>G (p.Ile299Val)not specified [RCV004841697]uncertain significance3183833759183833759Humanname
597658031CV3571490single nucleotide variantNM_018622.7(PARL):c.422A>C (p.Asp141Ala)not specified [RCV004827733]uncertain significance3183866665183866665Humanname
597719006CV3571491single nucleotide variantNM_018622.7(PARL):c.508A>T (p.Thr170Ser)not specified [RCV004841698]uncertain significance3183862756183862756Humanname
597719027CV3571494single nucleotide variantNM_018622.7(PARL):c.643A>G (p.Ser215Gly)not specified [RCV004841700]uncertain significance3183842412183842412Humanname
598259992CV4002039single nucleotide variantNM_018622.7(PARL):c.680A>G (p.Tyr227Cys)not specified [RCV005386596]uncertain significance3183842375183842375Humanname
156185717CV2292340single nucleotide variantNM_018622.7(PARL):c.1031G>T (p.Trp344Leu)not specified [RCV004150153]uncertain significance3183829707183829707Humanname
597718988CV3571488single nucleotide variantNM_018622.7(PARL):c.1076C>T (p.Pro359Leu)not specified [RCV004841696]uncertain significance3183829662183829662Humanname
597719036CV3571495single nucleotide variantNM_018622.7(PARL):c.1043A>T (p.Tyr348Phe)not specified [RCV004841701]uncertain significance3183829695183829695Humanname
598259997CV4002040single nucleotide variantNM_018622.7(PARL):c.1117A>C (p.Lys373Gln)not specified [RCV005386597]uncertain significance3183829621183829621Humanname
8630705CV85860single nucleotide variantNM_001037639.1(PARL):c.378C>T (p.Ser126=)Malignant melanoma [RCV000065944]not provided3183866709183866709Humanname
8630706CV85861single nucleotide variantNM_001037639.1(PARL):c.377C>T (p.Ser126Phe)Malignant melanoma [RCV000065945]not provided3183866710183866710Humanname