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Variants search result for Homo sapiens
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48 records found for search term Krt15
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155984569CV2241134single nucleotide variantNM_002275.4(KRT15):c.41G>A (p.Gly14Glu)not specified [RCV004104165]uncertain significance174151878741518787Humanname
156085530CV2244625single nucleotide variantNM_002275.4(KRT15):c.94G>A (p.Gly32Arg)not specified [RCV004102342]uncertain significance174151873441518734Humanname
156151007CV2318732single nucleotide variantNM_002275.4(KRT15):c.92G>A (p.Gly31Asp)not specified [RCV004175665]uncertain significance174151873641518736Humanname
329358183CV2453932single nucleotide variantNM_002275.4(KRT15):c.32C>A (p.Ser11Tyr)not specified [RCV004271316]uncertain significance174151879641518796Humanname
15136014CV715435single nucleotide variantNM_002275.4(KRT15):c.95G>A (p.Gly32Glu)not provided [RCV000965380]benign174151873341518733Humanname
156050561CV2378467single nucleotide variantNM_002275.4(KRT15):c.122G>A (p.Ser41Asn)not specified [RCV004228525]uncertain significance174151870641518706Humanname
401914279CV2811348single nucleotide variantNM_002275.4(KRT15):c.125G>A (p.Arg42Gln)not provided [RCV003428274]uncertain significance174151870341518703Humanname
405817269CV3272953single nucleotide variantNM_002275.4(KRT15):c.175G>A (p.Gly59Arg)not specified [RCV004412198]uncertain significance174151865341518653Humanname
407459884CV3445446single nucleotide variantNM_002275.4(KRT15):c.251G>A (p.Gly84Asp)not specified [RCV004633699]uncertain significance174151857741518577Humanname
598183997CV3980271single nucleotide variantNM_002275.4(KRT15):c.296G>A (p.Gly99Asp)not specified [RCV005352999]uncertain significance174151853241518532Humanname
598184003CV3980275single nucleotide variantNM_002275.4(KRT15):c.154G>A (p.Val52Ile)not specified [RCV005353000]uncertain significance174151867441518674Humanname
15193457CV755823single nucleotide variantNM_002275.4(KRT15):c.1083G>A (p.Leu361=)not provided [RCV000910845]likely benign174151563641515636Humanname
156279632CV2252178single nucleotide variantNM_002275.4(KRT15):c.664G>T (p.Ala222Ser)not specified [RCV004122192]uncertain significance174151688241516882Humanname
156258846CV2274064single nucleotide variantNM_002275.4(KRT15):c.548A>G (p.Asn183Ser)not specified [RCV004134716]uncertain significance174151711641517116Humanname
156061239CV2323156single nucleotide variantNM_002275.4(KRT15):c.490C>T (p.Arg164Trp)not specified [RCV004187560]uncertain significance174151833841518338Humanname
156157010CV2359906single nucleotide variantNM_002275.4(KRT15):c.473A>G (p.Lys158Arg)not specified [RCV004212755]uncertain significance174151835541518355Humanname
329352527CV2453152single nucleotide variantNM_002275.4(KRT15):c.667A>G (p.Arg223Gly)not specified [RCV004279533]uncertain significance174151687941516879Humanname
329395430CV2458361single nucleotide variantNM_002275.4(KRT15):c.880G>A (p.Glu294Lys)not specified [RCV004266001]uncertain significance174151612441516124Humanname
401742317CV2697749single nucleotide variantNM_002275.4(KRT15):c.598G>A (p.Ala200Thr)not specified [RCV004300480]uncertain significance174151694841516948Humanname
401758215CV2704229single nucleotide variantNM_002275.4(KRT15):c.751T>C (p.Phe251Leu)not specified [RCV004311229]uncertain significance174151625341516253Humanname
401880056CV2783079single nucleotide variantNM_002275.4(KRT15):c.454G>A (p.Asp152Asn)not specified [RCV004363440]uncertain significance174151837441518374Humanname
405817267CV3272955single nucleotide variantNM_002275.4(KRT15):c.728A>G (p.Asn243Ser)not specified [RCV004412200]uncertain significance174151681841516818Humanname
405817266CV3272956single nucleotide variantNM_002275.4(KRT15):c.843G>C (p.Gln281His)not specified [RCV004412201]uncertain significance174151616141516161Humanname
597794855CV3698373single nucleotide variantNM_002275.4(KRT15):c.789G>A (p.Met263Ile)not specified [RCV004934649]uncertain significance174151621541516215Humanname
597797869CV3698376single nucleotide variantNM_002275.4(KRT15):c.563C>T (p.Ala188Val)not specified [RCV004935947]uncertain significance174151710141517101Humanname
597797872CV3698377single nucleotide variantNM_002275.4(KRT15):c.371G>T (p.Arg124Leu)not specified [RCV004935948]uncertain significance174151845741518457Humanname
597794858CV3698379single nucleotide variantNM_002275.4(KRT15):c.344G>T (p.Arg115Leu)not specified [RCV004934650]uncertain significance174151848441518484Humanname
597797878CV3698380single nucleotide variantNM_002275.4(KRT15):c.901A>G (p.Thr301Ala)not specified [RCV004935950]uncertain significance174151601041516010Humanname
597797881CV3698381single nucleotide variantNM_002275.4(KRT15):c.704A>G (p.Glu235Gly)not specified [RCV004935951]uncertain significance174151684241516842Humanname
597797884CV3698382single nucleotide variantNM_002275.4(KRT15):c.679G>A (p.Glu227Lys)not specified [RCV004935952]uncertain significance174151686741516867Humanname
597797894CV3698385single nucleotide variantNM_002275.4(KRT15):c.522C>A (p.Asn174Lys)not specified [RCV004935955]uncertain significance174151714241517142Humanname
8636154CV91378single nucleotide variantNM_002275.3(KRT15):c.568G>A (p.Asp190Asn)Malignant melanoma [RCV000071476]not provided174151709641517096Humanname
156236273CV2193462single nucleotide variantNM_002275.4(KRT15):c.1220G>A (p.Arg407His)not specified [RCV004072950]uncertain significance174151549941515499Humanname
156041673CV2219591single nucleotide variantNM_002275.4(KRT15):c.1339C>A (p.Gln447Lys)not specified [RCV004095320]likely benign174151405541514055Humanname
155908261CV2302388single nucleotide variantNM_002275.4(KRT15):c.1130A>G (p.Glu377Gly)not specified [RCV004161135]uncertain significance174151558941515589Humanname
155974106CV2317828single nucleotide variantNM_002275.4(KRT15):c.1205A>G (p.Glu402Gly)not specified [RCV004175069]uncertain significance174151551441515514Humanname
155994828CV2377667single nucleotide variantNM_002275.4(KRT15):c.1210G>A (p.Ala404Thr)not specified [RCV004227843]uncertain significance174151550941515509Humanname
329380469CV2444405single nucleotide variantNM_002275.4(KRT15):c.1193G>A (p.Arg398Gln)not specified [RCV004263148]uncertain significance174151552641515526Humanname
401742923CV2715351single nucleotide variantNM_002275.4(KRT15):c.1023C>G (p.Ser341Arg)not specified [RCV004324683]uncertain significance174151588841515888Humanname
405817270CV3272952single nucleotide variantNM_002275.4(KRT15):c.1044C>G (p.Asn348Lys)not specified [RCV004412197]uncertain significance174151567541515675Humanname
597797863CV3698374single nucleotide variantNM_002275.4(KRT15):c.1184T>A (p.Ile395Lys)not specified [RCV004935945]uncertain significance174151553541515535Humanname
597797875CV3698378single nucleotide variantNM_002275.4(KRT15):c.1316A>G (p.Asn439Ser)not specified [RCV004935949]uncertain significance174151407841514078Humanname
597797887CV3698383single nucleotide variantNM_002275.4(KRT15):c.1066C>T (p.Arg356Cys)not specified [RCV004935953]uncertain significance174151565341515653Humanname
597797891CV3698384single nucleotide variantNM_002275.4(KRT15):c.1160A>C (p.Gln387Pro)not specified [RCV004935954]uncertain significance174151555941515559Humanname
598162712CV3980272single nucleotide variantNM_002275.4(KRT15):c.1111C>G (p.Leu371Val)not specified [RCV005368697]uncertain significance174151560841515608Humanname
598162720CV3980274single nucleotide variantNM_002275.4(KRT15):c.1138T>C (p.Cys380Arg)not specified [RCV005368699]uncertain significance174151558141515581Humanname
598162728CV3980276single nucleotide variantNM_002275.4(KRT15):c.1226T>C (p.Leu409Pro)not specified [RCV005368700]uncertain significance174151549341515493Humanname
598162735CV3980277single nucleotide variantNM_002275.4(KRT15):c.1030G>A (p.Ala344Thr)not specified [RCV005368701]uncertain significance174151568941515689Humanname