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Variants search result for Homo sapiens
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40 records found for search term Hoxd9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156188369CV2258391single nucleotide variantNM_014213.4(HOXD9):c.20G>A (p.Gly7Glu)not specified [RCV004115598]uncertain significance2176122788176122788Humanname
15195750CV697174single nucleotide variantNM_014213.4(HOXD9):c.20G>C (p.Gly7Ala)not provided [RCV000956010]benign2176122788176122788Humanname
597773029CV3679796single nucleotide variantNM_014213.4(HOXD9):c.97G>A (p.Val33Met)not specified [RCV004928802]uncertain significance2176122865176122865Humanname
15174271CV707863single nucleotide variantNM_014213.4(HOXD9):c.921C>T (p.Asn307=)not provided [RCV000972687]benign2176124037176124037Humanname
156278148CV2286719single nucleotide variantNM_014213.4(HOXD9):c.184G>C (p.Glu62Gln)not specified [RCV004142542]uncertain significance2176122952176122952Humanname
156390313CV2373300single nucleotide variantNM_014213.4(HOXD9):c.167C>T (p.Pro56Leu)not specified [RCV004220011]uncertain significance2176122935176122935Humanname
329360373CV2458700single nucleotide variantNM_014213.4(HOXD9):c.196T>C (p.Cys66Arg)not specified [RCV004268361]uncertain significance2176122964176122964Humanname
405798041CV3263491single nucleotide variantNM_014213.4(HOXD9):c.107C>A (p.Ala36Glu)not specified [RCV004402130]uncertain significance2176122875176122875Humanname
155972300CV2228131single nucleotide variantNM_014213.4(HOXD9):c.353C>T (p.Ser118Phe)not specified [RCV004096350]uncertain significance2176123121176123121Humanname
156389138CV2229958single nucleotide variantNM_014213.4(HOXD9):c.839T>G (p.Ile280Ser)not specified [RCV004105492]uncertain significance2176123955176123955Humanname
156251558CV2273413single nucleotide variantNM_014213.4(HOXD9):c.299T>G (p.Val100Gly)not specified [RCV004132175]uncertain significance2176123067176123067Humanname
156265890CV2275432single nucleotide variantNM_014213.4(HOXD9):c.650C>A (p.Ala217Glu)not specified [RCV004135308]uncertain significance2176123418176123418Humanname
156193524CV2301991single nucleotide variantNM_014213.4(HOXD9):c.673G>C (p.Gly225Arg)not specified [RCV004158763]uncertain significance2176123441176123441Humanname
156306766CV2335278single nucleotide variantNM_014213.4(HOXD9):c.466C>A (p.Arg156Ser)not specified [RCV004186845]uncertain significance2176123234176123234Humanname
156331600CV2339662single nucleotide variantNM_014213.4(HOXD9):c.741C>G (p.Asp247Glu)not specified [RCV004196367]uncertain significance2176123509176123509Humanname
329374707CV2470679single nucleotide variantNM_014213.4(HOXD9):c.805C>G (p.Gln269Glu)not specified [RCV004275929]uncertain significance2176123573176123573Humanname
401736150CV2672836single nucleotide variantNM_014213.4(HOXD9):c.458C>G (p.Ala153Gly)not specified [RCV004281612]uncertain significance2176123226176123226Humanname
401758630CV2700653single nucleotide variantNM_014213.4(HOXD9):c.719C>T (p.Ser240Leu)not specified [RCV004313373]uncertain significance2176123487176123487Humanname
405268548CV3198994single nucleotide variantNM_014213.4(HOXD9):c.463G>T (p.Gly155Trp)HOXD9-related disorder [RCV003912105]likely benign2176123231176123231Humanname , trait , alternate_id
405272692CV3210118single nucleotide variantNM_014213.4(HOXD9):c.334C>A (p.Pro112Thr)HOXD9-related disorder [RCV003914367]likely benign2176123102176123102Humanname , trait , alternate_id
405295098CV3211036single nucleotide variantNM_014213.4(HOXD9):c.463G>C (p.Gly155Arg)HOXD9-related disorder [RCV003937037]likely benign2176123231176123231Humanname , trait , alternate_id
405798295CV3263492single nucleotide variantNM_014213.4(HOXD9):c.418G>A (p.Gly140Ser)not specified [RCV004402131]uncertain significance2176123186176123186Humanname
405798047CV3263493single nucleotide variantNM_014213.4(HOXD9):c.544A>G (p.Thr182Ala)not specified [RCV004402132]uncertain significance2176123312176123312Humanname
405798050CV3263494single nucleotide variantNM_014213.4(HOXD9):c.667G>A (p.Gly223Arg)not specified [RCV004402133]uncertain significance2176123435176123435Humanname
405798053CV3263495single nucleotide variantNM_014213.4(HOXD9):c.878C>G (p.Thr293Ser)not specified [RCV004402134]uncertain significance2176123994176123994Humanname
405798056CV3263496single nucleotide variantNM_014213.4(HOXD9):c.924G>T (p.Met308Ile)not specified [RCV004402135]uncertain significance2176124040176124040Humanname
407528185CV3433858single nucleotide variantNM_014213.4(HOXD9):c.590G>A (p.Arg197Gln)not specified [RCV004633057]uncertain significance2176123358176123358Humanname
597773002CV3679791single nucleotide variantNM_014213.4(HOXD9):c.337G>T (p.Gly113Cys)not specified [RCV004928797]uncertain significance2176123105176123105Humanname
597773008CV3679792single nucleotide variantNM_014213.4(HOXD9):c.586G>A (p.Ala196Thr)not specified [RCV004928798]uncertain significance2176123354176123354Humanname
597773013CV3679793single nucleotide variantNM_014213.4(HOXD9):c.638T>C (p.Leu213Pro)not specified [RCV004928799]uncertain significance2176123406176123406Humanname
597773019CV3679794single nucleotide variantNM_014213.4(HOXD9):c.792G>C (p.Gln264His)not specified [RCV004928800]uncertain significance2176123560176123560Humanname
597773024CV3679795single nucleotide variantNM_014213.4(HOXD9):c.775G>A (p.Glu259Lys)not specified [RCV004928801]uncertain significance2176123543176123543Humanname
597773034CV3679797single nucleotide variantNM_014213.4(HOXD9):c.545C>T (p.Thr182Ile)not specified [RCV004928803]uncertain significance2176123313176123313Humanname
597773039CV3679798single nucleotide variantNM_014213.4(HOXD9):c.347T>C (p.Val116Ala)not specified [RCV004928804]uncertain significance2176123115176123115Humanname
597773047CV3679799single nucleotide variantNM_014213.4(HOXD9):c.305C>A (p.Pro102Gln)not specified [RCV004928805]uncertain significance2176123073176123073Humanname
597773052CV3679800single nucleotide variantNM_014213.4(HOXD9):c.605G>A (p.Ser202Asn)not specified [RCV004928806]uncertain significance2176123373176123373Humanname
598192300CV3971830single nucleotide variantNM_014213.4(HOXD9):c.668G>T (p.Gly223Val)not specified [RCV005354422]uncertain significance2176123436176123436Humanname
598192307CV3971831single nucleotide variantNM_014213.4(HOXD9):c.515C>T (p.Thr172Met)not specified [RCV005354423]uncertain significance2176123283176123283Humanname
598192314CV3971832single nucleotide variantNM_014213.4(HOXD9):c.973A>C (p.Thr325Pro)not specified [RCV005354424]uncertain significance2176124089176124089Humanname
156274267CV2334096single nucleotide variantNM_014213.4(HOXD9):c.1046C>T (p.Pro349Leu)not specified [RCV004183611]uncertain significance2176124162176124162Humanname