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Variants search result for Homo sapiens
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35 records found for search term Dhrs9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405691893CV3247090single nucleotide variantNM_001376924.1(DHRS9):c.22C>T (p.Leu8Phe)not specified [RCV004373469]uncertain significance2169081603169081603Humanname
597659404CV3652251single nucleotide variantNM_001376924.1(DHRS9):c.63A>T (p.Lys21Asn)not specified [RCV004911646]uncertain significance2169081644169081644Humanname
156332837CV2270389single nucleotide variantNM_001376924.1(DHRS9):c.202G>C (p.Ala68Pro)not specified [RCV004135583]uncertain significance2169081783169081783Humanname
597659380CV3652247single nucleotide variantNM_001376924.1(DHRS9):c.137C>T (p.Ala46Val)not specified [RCV004911642]uncertain significance2169081718169081718Humanname
597659390CV3652249single nucleotide variantNM_001376924.1(DHRS9):c.249T>G (p.Asp83Glu)not specified [RCV004911644]uncertain significance2169081830169081830Humanname
156319527CV2200544single nucleotide variantNM_001376924.1(DHRS9):c.671T>A (p.Leu224His)not specified [RCV004078892]uncertain significance2169091888169091888Humanname
156113911CV2208863single nucleotide variantNM_001376924.1(DHRS9):c.641C>T (p.Ala214Val)not specified [RCV004085241]uncertain significance2169091858169091858Humanname
155980850CV2212060single nucleotide variantNM_001376924.1(DHRS9):c.558C>G (p.Phe186Leu)not specified [RCV004088970]uncertain significance2169083573169083573Humanname
155932278CV2232047single nucleotide variantNM_001376924.1(DHRS9):c.601G>A (p.Val201Ile)not specified [RCV004093095]uncertain significance2169091818169091818Humanname
155965579CV2261810single nucleotide variantNM_001376924.1(DHRS9):c.350G>T (p.Gly117Val)not specified [RCV004126086]uncertain significance2169083365169083365Humanname
155900934CV2298090single nucleotide variantNM_001376924.1(DHRS9):c.479T>A (p.Ile160Asn)not specified [RCV004157978]uncertain significance2169083494169083494Humanname
156306940CV2335316single nucleotide variantNM_001376924.1(DHRS9):c.352G>A (p.Val118Met)not specified [RCV004186878]uncertain significance2169083367169083367Humanname
156305217CV2369397single nucleotide variantNM_001376924.1(DHRS9):c.821G>A (p.Ser274Asn)not specified [RCV004210346]uncertain significance2169095628169095628Humanname
155992733CV2379343single nucleotide variantNM_001376924.1(DHRS9):c.818C>G (p.Thr273Arg)not specified [RCV004223803]uncertain significance2169095625169095625Humanname
156169696CV2400505single nucleotide variantNM_001376924.1(DHRS9):c.847G>A (p.Ala283Thr)not specified [RCV004246703]uncertain significance2169095654169095654Humanname
401736429CV2683019single nucleotide variantNM_001376924.1(DHRS9):c.670C>T (p.Leu224Phe)not specified [RCV004283802]uncertain significance2169091887169091887Humanname
401731290CV2693713single nucleotide variantNM_001376924.1(DHRS9):c.823C>T (p.Leu275Phe)not specified [RCV004298041]uncertain significance2169095630169095630Humanname
401737491CV2699830single nucleotide variantNM_001376924.1(DHRS9):c.502C>T (p.Arg168Cys)not specified [RCV004308475]uncertain significance2169083517169083517Humanname
401720233CV2705771single nucleotide variantNM_001376924.1(DHRS9):c.863A>G (p.Lys288Arg)not specified [RCV004318607]uncertain significance2169095670169095670Humanname
401753246CV2722405single nucleotide variantNM_001376924.1(DHRS9):c.610A>G (p.Ile204Val)not specified [RCV004322808]uncertain significance2169091827169091827Humanname
401767973CV2727339single nucleotide variantNM_001376924.1(DHRS9):c.361C>T (p.Pro121Ser)not specified [RCV004327445]uncertain significance2169083376169083376Humanname
401898664CV2787997single nucleotide variantNM_001376924.1(DHRS9):c.575G>A (p.Arg192Gln)not specified [RCV004358650]uncertain significance2169091792169091792Humanname
405691902CV3247091single nucleotide variantNM_001376924.1(DHRS9):c.401T>C (p.Ile134Thr)not specified [RCV004373470]uncertain significance2169083416169083416Humanname
405691907CV3247092single nucleotide variantNM_001376924.1(DHRS9):c.511A>T (p.Ile171Phe)not specified [RCV004373471]likely benign2169083526169083526Humanname
405691913CV3247093single nucleotide variantNM_001376924.1(DHRS9):c.554G>T (p.Gly185Val)not specified [RCV004373472]uncertain significance2169083569169083569Humanname
405691918CV3247094single nucleotide variantNM_001376924.1(DHRS9):c.673G>A (p.Ala225Thr)not specified [RCV004373473]uncertain significance2169091890169091890Humanname
405691924CV3247095single nucleotide variantNM_001376924.1(DHRS9):c.838C>A (p.His280Asn)not specified [RCV004373474]uncertain significance2169095645169095645Humanname
407467180CV3434087single nucleotide variantNM_001376924.1(DHRS9):c.586G>A (p.Ala196Thr)not specified [RCV004614148]uncertain significance2169091803169091803Humanname
407467184CV3434088single nucleotide variantNM_001376924.1(DHRS9):c.302T>C (p.Val101Ala)not specified [RCV004614149]uncertain significance2169081883169081883Humanname
407467188CV3434089single nucleotide variantNM_001376924.1(DHRS9):c.403G>A (p.Glu135Lys)not specified [RCV004614150]uncertain significance2169083418169083418Humanname
407467196CV3434091single nucleotide variantNM_001376924.1(DHRS9):c.850G>A (p.Gly284Arg)not specified [RCV004614152]uncertain significance2169095657169095657Humanname
597659386CV3652248single nucleotide variantNM_001376924.1(DHRS9):c.413T>C (p.Leu138Pro)not specified [RCV004911643]uncertain significance2169083428169083428Humanname
597659395CV3652250single nucleotide variantNM_001376924.1(DHRS9):c.700A>T (p.Ile234Phe)not specified [RCV004911645]uncertain significance2169091917169091917Humanname
597659409CV3652252single nucleotide variantNM_001376924.1(DHRS9):c.764C>T (p.Ser255Phe)not specified [RCV004911647]uncertain significance2169095571169095571Humanname
598162194CV3953086single nucleotide variantNM_001376924.1(DHRS9):c.703A>G (p.Lys235Glu)not specified [RCV005329121]uncertain significance2169091920169091920Humanname