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46 records found for search term Tspyl4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156329909CV2216519single nucleotide variantNM_021648.5(TSPYL4):c.13G>A (p.Asp5Asn)not specified [RCV004097317]uncertain significance6116253996116253996Humanname
405799069CV3340966single nucleotide variantNM_021648.5(TSPYL4):c.20G>A (p.Gly7Asp)not specified [RCV004476711]uncertain significance6116253989116253989Humanname
401920876CV2820650single nucleotide variantNM_021648.5(TSPYL4):c.687G>A (p.Glu229=)not provided [RCV003432014]likely benign6116253322116253322Humanname
405799074CV3340968single nucleotide variantNM_021648.5(TSPYL4):c.34C>G (p.Leu12Val)not specified [RCV004476713]likely benign6116253975116253975Humanname
156091562CV2216652single nucleotide variantNM_021648.5(TSPYL4):c.151G>A (p.Gly51Arg)not specified [RCV004083109]uncertain significance6116253858116253858Humanname
156255567CV2277517single nucleotide variantNM_021648.5(TSPYL4):c.110G>C (p.Arg37Pro)not specified [RCV004145207]uncertain significance6116253899116253899Humanname
401724978CV2715050single nucleotide variantNM_021648.5(TSPYL4):c.121G>A (p.Glu41Lys)not specified [RCV004322360]uncertain significance6116253888116253888Humanname
401886853CV2776780single nucleotide variantNM_021648.5(TSPYL4):c.177G>T (p.Glu59Asp)not specified [RCV004357928]uncertain significance6116253832116253832Humanname
156344017CV2229596single nucleotide variantNM_021648.5(TSPYL4):c.377C>T (p.Ala126Val)not specified [RCV004103413]uncertain significance6116253632116253632Humanname
156073831CV2230020single nucleotide variantNM_021648.5(TSPYL4):c.628A>G (p.Ile210Val)not specified [RCV004105821]uncertain significance6116253381116253381Humanname
155948321CV2245906single nucleotide variantNM_021648.5(TSPYL4):c.725G>A (p.Arg242His)not specified [RCV004111744]uncertain significance6116253284116253284Humanname
156020864CV2264401single nucleotide variantNM_021648.5(TSPYL4):c.639G>C (p.Glu213Asp)not specified [RCV004138301]uncertain significance6116253370116253370Humanname
155915840CV2274418single nucleotide variantNM_021648.5(TSPYL4):c.367C>T (p.Arg123Cys)not specified [RCV004136788]uncertain significance6116253642116253642Humanname
155966620CV2284404single nucleotide variantNM_021648.5(TSPYL4):c.888C>G (p.Phe296Leu)not specified [RCV004146741]uncertain significance6116253121116253121Humanname
156040576CV2310816single nucleotide variantNM_021648.5(TSPYL4):c.656C>A (p.Ala219Asp)not specified [RCV004163867]uncertain significance6116253353116253353Humanname
155973491CV2321054single nucleotide variantNM_021648.5(TSPYL4):c.552G>T (p.Lys184Asn)not specified [RCV004172840]uncertain significance6116253457116253457Humanname
156174558CV2377177single nucleotide variantNM_021648.5(TSPYL4):c.545A>G (p.Glu182Gly)not specified [RCV004231852]uncertain significance6116253464116253464Humanname
156106892CV2387104single nucleotide variantNM_021648.5(TSPYL4):c.319G>A (p.Glu107Lys)not specified [RCV004226840]uncertain significance6116253690116253690Humanname
401881832CV2774627single nucleotide variantNM_021648.5(TSPYL4):c.368G>T (p.Arg123Leu)not specified [RCV004350095]uncertain significance6116253641116253641Humanname
405799071CV3340967single nucleotide variantNM_021648.5(TSPYL4):c.301G>A (p.Glu101Lys)not specified [RCV004476712]uncertain significance6116253708116253708Humanname
405799081CV3340970single nucleotide variantNM_021648.5(TSPYL4):c.463A>G (p.Lys155Glu)not specified [RCV004476715]uncertain significance6116253546116253546Humanname
405799083CV3340971single nucleotide variantNM_021648.5(TSPYL4):c.515C>T (p.Ala172Val)not specified [RCV004476716]likely benign6116253494116253494Humanname
405799086CV3340972single nucleotide variantNM_021648.5(TSPYL4):c.575A>G (p.Glu192Gly)not specified [RCV004476717]uncertain significance6116253434116253434Humanname
405799093CV3340974single nucleotide variantNM_021648.5(TSPYL4):c.845T>C (p.Leu282Ser)not specified [RCV004476719]uncertain significance6116253164116253164Humanname
405799096CV3340975single nucleotide variantNM_021648.5(TSPYL4):c.850G>C (p.Val284Leu)not specified [RCV004476720]uncertain significance6116253159116253159Humanname
407461939CV3487081single nucleotide variantNM_021648.5(TSPYL4):c.873A>C (p.Arg291Ser)not specified [RCV004687793]uncertain significance6116253136116253136Humanname
597788487CV3618125single nucleotide variantNM_021648.5(TSPYL4):c.778A>C (p.Asn260His)not specified [RCV004875873]uncertain significance6116253231116253231Humanname
597788491CV3618127single nucleotide variantNM_021648.5(TSPYL4):c.949C>T (p.Arg317Cys)not specified [RCV004875874]uncertain significance6116253060116253060Humanname
597788499CV3618129single nucleotide variantNM_021648.5(TSPYL4):c.973T>G (p.Ser325Ala)not specified [RCV004875876]uncertain significance6116253036116253036Humanname
597788503CV3618130single nucleotide variantNM_021648.5(TSPYL4):c.638A>T (p.Glu213Val)not specified [RCV004875877]uncertain significance6116253371116253371Humanname
597788507CV3618131single nucleotide variantNM_021648.5(TSPYL4):c.988A>G (p.Ile330Val)not specified [RCV004875878]uncertain significance6116253021116253021Humanname
598216876CV3924971single nucleotide variantNM_021648.5(TSPYL4):c.335G>A (p.Ser112Asn)not specified [RCV005292943]uncertain significance6116253674116253674Humanname
598216885CV3924973single nucleotide variantNM_021648.5(TSPYL4):c.785C>T (p.Pro262Leu)not specified [RCV005292944]uncertain significance6116253224116253224Humanname
598238536CV3924974single nucleotide variantNM_021648.5(TSPYL4):c.784C>T (p.Pro262Ser)not specified [RCV005296432]uncertain significance6116253225116253225Humanname
598238541CV3924976single nucleotide variantNM_021648.5(TSPYL4):c.965G>T (p.Arg322Leu)not specified [RCV005296433]uncertain significance6116253044116253044Humanname
156291492CV2321115single nucleotide variantNM_021648.5(TSPYL4):c.1236G>C (p.Gln412His)not specified [RCV004175249]uncertain significance6116252773116252773Humanname
156183743CV2382271single nucleotide variantNM_021648.5(TSPYL4):c.1037G>A (p.Arg346Gln)not specified [RCV004228211]uncertain significance6116252972116252972Humanname
401778475CV2709168single nucleotide variantNM_021648.5(TSPYL4):c.1001G>C (p.Arg334Pro)not specified [RCV004316352]uncertain significance6116253008116253008Humanname
401896066CV2777395single nucleotide variantNM_021648.5(TSPYL4):c.1085G>A (p.Ser362Asn)not specified [RCV004354395]uncertain significance6116252924116252924Humanname
405799062CV3340963single nucleotide variantNM_021648.5(TSPYL4):c.1090C>A (p.Leu364Ile)not specified [RCV004476708]uncertain significance6116252919116252919Humanname
405799066CV3340965single nucleotide variantNM_021648.5(TSPYL4):c.1216G>A (p.Ala406Thr)not specified [RCV004476710]uncertain significance6116252793116252793Humanname
597788477CV3618123single nucleotide variantNM_021648.5(TSPYL4):c.1012C>T (p.Pro338Ser)not specified [RCV004875871]uncertain significance6116252997116252997Humanname
597788483CV3618124single nucleotide variantNM_021648.5(TSPYL4):c.1111G>A (p.Glu371Lys)not specified [RCV004875872]uncertain significance6116252898116252898Humanname
597788495CV3618128single nucleotide variantNM_021648.5(TSPYL4):c.1027C>T (p.His343Tyr)not specified [RCV004875875]uncertain significance6116252982116252982Humanname
598238530CV3924972single nucleotide variantNM_021648.5(TSPYL4):c.1178G>A (p.Arg393Lys)not specified [RCV005296431]uncertain significance6116252831116252831Humanname
598216893CV3924975single nucleotide variantNM_021648.5(TSPYL4):c.1177A>G (p.Arg393Gly)not specified [RCV005292945]uncertain significance6116252832116252832Humanname