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Variants search result for Homo sapiens
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46 records found for search term Sgpp1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597673233CV3595758single nucleotide variantNM_030791.4(SGPP1):c.5C>T (p.Ser2Leu)not specified [RCV004856663]uncertain significance146372794063727940Humanname
401902049CV2810460single nucleotide variantNM_030791.4(SGPP1):c.327C>T (p.Arg109=)not provided [RCV003393458]likely benign146372761863727618Humanname
407492799CV3484108single nucleotide variantNM_030791.4(SGPP1):c.52C>G (p.Gln18Glu)not specified [RCV004667231]uncertain significance146372789363727893Humanname
598166950CV3921245single nucleotide variantNM_030791.4(SGPP1):c.64C>T (p.Arg22Cys)not specified [RCV005283751]uncertain significance146372788163727881Humanname
156072461CV2331510single nucleotide variantNM_030791.4(SGPP1):c.290T>C (p.Leu97Pro)not specified [RCV004182116]uncertain significance146372765563727655Humanname
156177868CV2355885single nucleotide variantNM_030791.4(SGPP1):c.112G>C (p.Asp38His)not specified [RCV004201274]uncertain significance146372783363727833Humanname
401871251CV2763445single nucleotide variantNM_030791.4(SGPP1):c.238C>G (p.Pro80Ala)not specified [RCV004349333]uncertain significance146372770763727707Humanname
405706917CV3321640single nucleotide variantNM_030791.4(SGPP1):c.253G>T (p.Ala85Ser)not specified [RCV004447914]uncertain significance146372769263727692Humanname
597673249CV3595760single nucleotide variantNM_030791.4(SGPP1):c.230C>G (p.Pro77Arg)not specified [RCV004856665]uncertain significance146372771563727715Humanname
597673488CV3595762single nucleotide variantNM_030791.4(SGPP1):c.296C>A (p.Pro99Gln)not specified [RCV004856667]uncertain significance146372764963727649Humanname
598166926CV3921241single nucleotide variantNM_030791.4(SGPP1):c.173G>A (p.Arg58Gln)not specified [RCV005283747]uncertain significance146372777263727772Humanname
598166944CV3921244single nucleotide variantNM_030791.4(SGPP1):c.209G>A (p.Gly70Glu)not specified [RCV005283750]uncertain significance146372773663727736Humanname
156324692CV2198836single nucleotide variantNM_030791.4(SGPP1):c.886A>G (p.Ile296Val)not specified [RCV004077875]uncertain significance146368654563686545Humanname
155921028CV2212089single nucleotide variantNM_030791.4(SGPP1):c.848A>G (p.Asn283Ser)not specified [RCV004088998]uncertain significance146368658363686583Humanname
156030321CV2278708single nucleotide variantNM_030791.4(SGPP1):c.913T>C (p.Phe305Leu)not specified [RCV004134902]uncertain significance146368651863686518Humanname
156297376CV2297671single nucleotide variantNM_030791.4(SGPP1):c.997T>G (p.Ser333Ala)not specified [RCV004155356]uncertain significance146368643463686434Humanname
156288597CV2299215single nucleotide variantNM_030791.4(SGPP1):c.305C>A (p.Pro102Gln)not specified [RCV004152549]uncertain significance146372764063727640Humanname
156288999CV2299279single nucleotide variantNM_030791.4(SGPP1):c.353G>A (p.Gly118Asp)not specified [RCV004152605]uncertain significance146372759263727592Humanname
156012275CV2358876single nucleotide variantNM_030791.4(SGPP1):c.304C>T (p.Pro102Ser)not specified [RCV004212219]uncertain significance146372764163727641Humanname
156306365CV2359929single nucleotide variantNM_030791.4(SGPP1):c.854A>C (p.Asn285Thr)not specified [RCV004212774]uncertain significance146368657763686577Humanname
156257417CV2374290single nucleotide variantNM_030791.4(SGPP1):c.961G>A (p.Glu321Lys)not specified [RCV004229422]uncertain significance146368647063686470Humanname
156084653CV2395240single nucleotide variantNM_030791.4(SGPP1):c.319G>A (p.Ala107Thr)not specified [RCV004236902]uncertain significance146372762663727626Humanname
329393873CV2449923single nucleotide variantNM_030791.4(SGPP1):c.671A>G (p.Tyr224Cys)not specified [RCV004268997]uncertain significance146372727463727274Humanname
401756794CV2696492single nucleotide variantNM_030791.4(SGPP1):c.365G>A (p.Arg122His)not specified [RCV004312563]likely benign146372758063727580Humanname
401748511CV2696493single nucleotide variantNM_030791.4(SGPP1):c.389G>A (p.Cys130Tyr)not specified [RCV004312564]likely benign146372755663727556Humanname
401748516CV2696494single nucleotide variantNM_030791.4(SGPP1):c.402C>G (p.Phe134Leu)not specified [RCV004312565]uncertain significance146372754363727543Humanname
401748521CV2696495single nucleotide variantNM_030791.4(SGPP1):c.435C>G (p.Ile145Met)not specified [RCV004312566]uncertain significance146372751063727510Humanname
401748526CV2696496single nucleotide variantNM_030791.4(SGPP1):c.469C>G (p.Pro157Ala)not specified [RCV004312567]likely benign146372747663727476Humanname
401756796CV2696497single nucleotide variantNM_030791.4(SGPP1):c.509T>C (p.Val170Ala)not specified [RCV004312568]uncertain significance146372743663727436Humanname
401897092CV2789812single nucleotide variantNM_030791.4(SGPP1):c.587T>C (p.Val196Ala)not specified [RCV004362206]uncertain significance146372735863727358Humanname
405706923CV3321641single nucleotide variantNM_030791.4(SGPP1):c.364C>T (p.Arg122Cys)not specified [RCV004447915]uncertain significance146372758163727581Humanname
407490233CV3484109single nucleotide variantNM_030791.4(SGPP1):c.302C>T (p.Ser101Leu)not specified [RCV004666246]uncertain significance146372764363727643Humanname
407490236CV3484111single nucleotide variantNM_030791.4(SGPP1):c.311G>A (p.Arg104His)not specified [RCV004666247]uncertain significance146372763463727634Humanname
407490239CV3484112single nucleotide variantNM_030791.4(SGPP1):c.649A>G (p.Ile217Val)not specified [RCV004666248]uncertain significance146372729663727296Humanname
407492807CV3484113single nucleotide variantNM_030791.4(SGPP1):c.664C>T (p.Leu222Phe)not specified [RCV004667233]uncertain significance146372728163727281Humanname
597673256CV3595761single nucleotide variantNM_030791.4(SGPP1):c.329G>T (p.Arg110Leu)not specified [RCV004856666]uncertain significance146372761663727616Humanname
598166931CV3921242single nucleotide variantNM_030791.4(SGPP1):c.328C>A (p.Arg110Ser)not specified [RCV005283748]uncertain significance146372761763727617Humanname
156355618CV2324519single nucleotide variantNM_030791.4(SGPP1):c.1193C>T (p.Pro398Leu)not specified [RCV004178998]uncertain significance146368623863686238Humanname
156287897CV2327363single nucleotide variantNM_030791.4(SGPP1):c.1259A>G (p.Tyr420Cys)not specified [RCV004174794]uncertain significance146368617263686172Humanname
156345776CV2356361single nucleotide variantNM_030791.4(SGPP1):c.1066C>T (p.Pro356Ser)not specified [RCV004206164]uncertain significance146368636563686365Humanname
401719526CV2701158single nucleotide variantNM_030791.4(SGPP1):c.1208G>A (p.Arg403Gln)not specified [RCV004309740]uncertain significance146368622363686223Humanname
401717854CV2704042single nucleotide variantNM_030791.4(SGPP1):c.1112T>C (p.Ile371Thr)not specified [RCV004308925]uncertain significance146368631963686319Humanname
407492794CV3484106single nucleotide variantNM_030791.4(SGPP1):c.1117A>T (p.Met373Leu)not specified [RCV004667230]uncertain significance146368631463686314Humanname
407490230CV3484107single nucleotide variantNM_030791.4(SGPP1):c.1247G>A (p.Arg416Gln)not specified [RCV004666245]uncertain significance146368618463686184Humanname
597673242CV3595759single nucleotide variantNM_030791.4(SGPP1):c.1101G>C (p.Leu367Phe)not specified [RCV004856664]uncertain significance146368633063686330Humanname
598166937CV3921243single nucleotide variantNM_030791.4(SGPP1):c.1220A>G (p.Gln407Arg)not specified [RCV005283749]uncertain significance146368621163686211Humanname