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Variants search result for Homo sapiens
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50 records found for search term Sdf4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405760866CV3314268single nucleotide variantNM_016176.6(SDF4):c.-3G>Anot specified [RCV004455283]uncertain significance112287751228775Humanname
155918633CV2279262single nucleotide variantNM_016176.6(SDF4):c.-11C>Tnot specified [RCV004139784]uncertain significance112287831228783Humanname
156388992CV2376285single nucleotide variantNM_016176.6(SDF4):c.17G>A (p.Gly6Asp)not specified [RCV004220502]uncertain significance112287561228756Humanname
405760889CV3314272single nucleotide variantNM_016176.6(SDF4):c.20C>G (p.Pro7Arg)not specified [RCV004455287]uncertain significance112287531228753Humanname
15112142CV706638single nucleotide variantNM_016176.6(SDF4):c.105G>A (p.Ser35=)not provided [RCV000961246]benign112286681228668Humanname
156235053CV2193363single nucleotide variantNM_016176.6(SDF4):c.80C>T (p.Ala27Val)not specified [RCV004072866]likely benign112286931228693Humanname
155921186CV2207113single nucleotide variantNM_016176.6(SDF4):c.295A>G (p.Ile99Val)not specified [RCV004086064]uncertain significance112284781228478Humanname
156284676CV2349038single nucleotide variantNM_016176.6(SDF4):c.272G>A (p.Arg91Gln)not specified [RCV004205479]uncertain significance112285011228501Humanname
401760642CV2695112single nucleotide variantNM_016176.6(SDF4):c.254A>G (p.Glu85Gly)not specified [RCV004303268]uncertain significance112285191228519Humanname
405760872CV3314269single nucleotide variantNM_016176.6(SDF4):c.191G>A (p.Gly64Glu)not specified [RCV004455284]uncertain significance112285821228582Humanname
405760877CV3314270single nucleotide variantNM_016176.6(SDF4):c.258C>G (p.Asp86Glu)not specified [RCV004455285]uncertain significance112285151228515Humanname
405760883CV3314271single nucleotide variantNM_016176.6(SDF4):c.269G>A (p.Arg90Gln)not specified [RCV004455286]uncertain significance112285041228504Humanname
407491646CV3480343single nucleotide variantNM_016176.6(SDF4):c.135G>C (p.Glu45Asp)not specified [RCV004666942]uncertain significance112286381228638Humanname
407462068CV3480352single nucleotide variantNM_016176.6(SDF4):c.169G>A (p.Gly57Arg)not specified [RCV004658936]uncertain significance112286041228604Humanname
597713063CV3595092single nucleotide variantNM_016176.6(SDF4):c.253G>A (p.Glu85Lys)not specified [RCV004861235]uncertain significance112285201228520Humanname
598236559CV3906873single nucleotide variantNM_016176.6(SDF4):c.271C>T (p.Arg91Trp)not specified [RCV005275453]uncertain significance112285021228502Humanname
155967969CV2216940single nucleotide variantNM_016176.6(SDF4):c.491G>A (p.Gly164Asp)not specified [RCV004083349]uncertain significance112233091223309Humanname
155973354CV2271633single nucleotide variantNM_016176.6(SDF4):c.419G>A (p.Arg140His)not specified [RCV004130494]uncertain significance112238551223855Humanname
155983867CV2275237single nucleotide variantNM_016176.6(SDF4):c.464A>G (p.Tyr155Cys)not specified [RCV004137023]uncertain significance112233361223336Humanname
155900910CV2345695single nucleotide variantNM_016176.6(SDF4):c.508G>A (p.Val170Ile)not specified [RCV004205636]uncertain significance112232921223292Humanname
156155692CV2359750single nucleotide variantNM_016176.6(SDF4):c.482C>T (p.Ala161Val)not specified [RCV004210566]uncertain significance112233181223318Humanname
155930375CV2366745single nucleotide variantNM_016176.6(SDF4):c.798C>G (p.Asp266Glu)not specified [RCV004210744]uncertain significance112185511218551Humanname
156062394CV2380369single nucleotide variantNM_016176.6(SDF4):c.736C>T (p.Leu246Phe)not specified [RCV004217979]uncertain significance112186131218613Humanname
155967519CV2391353single nucleotide variantNM_016176.6(SDF4):c.494A>G (p.His165Arg)not specified [RCV004239760]uncertain significance112233061223306Humanname
329398504CV2471126single nucleotide variantNM_016176.6(SDF4):c.331A>G (p.Ile111Val)not specified [RCV004278379]uncertain significance112239431223943Humanname
401736021CV2689237single nucleotide variantNM_016176.6(SDF4):c.865G>A (p.Gly289Ser)not specified [RCV004306082]uncertain significance112184841218484Humanname
401731084CV2707698single nucleotide variantNM_016176.6(SDF4):c.376G>A (p.Glu126Lys)not specified [RCV004306955]uncertain significance112238981223898Humanname
401749851CV2719423single nucleotide variantNM_016176.6(SDF4):c.524G>A (p.Arg175Lys)not specified [RCV004326826]likely benign112232761223276Humanname
405760902CV3310382single nucleotide variantNM_016176.6(SDF4):c.418C>T (p.Arg140Cys)not specified [RCV004455289]uncertain significance112238561223856Humanname
405760908CV3310383single nucleotide variantNM_016176.6(SDF4):c.448G>T (p.Val150Leu)not specified [RCV004455290]uncertain significance112233521223352Humanname
405760913CV3310384single nucleotide variantNM_016176.6(SDF4):c.520A>G (p.Ile174Val)not specified [RCV004455291]uncertain significance112232801223280Humanname
405760918CV3310385single nucleotide variantNM_016176.6(SDF4):c.799A>G (p.Ile267Val)not specified [RCV004455292]uncertain significance112185501218550Humanname
405760924CV3310386single nucleotide variantNM_016176.6(SDF4):c.877G>A (p.Ala293Thr)not specified [RCV004455293]uncertain significance112184721218472Humanname
405760896CV3314273single nucleotide variantNM_016176.6(SDF4):c.415T>C (p.Phe139Leu)not specified [RCV004455288]uncertain significance112238591223859Humanname
407491650CV3480344single nucleotide variantNM_016176.6(SDF4):c.920A>G (p.Asn307Ser)not specified [RCV004666943]uncertain significance112176601217660Humanname
407462056CV3480345single nucleotide variantNM_016176.6(SDF4):c.989A>G (p.Glu330Gly)not specified [RCV004658932]uncertain significance112175911217591Humanname
407462062CV3480348single nucleotide variantNM_016176.6(SDF4):c.326G>A (p.Arg109Gln)not specified [RCV004658934]uncertain significance112239481223948Humanname
407491659CV3480349single nucleotide variantNM_016176.6(SDF4):c.550G>A (p.Glu184Lys)not specified [RCV004666945]uncertain significance112232501223250Humanname
407491664CV3480350single nucleotide variantNM_016176.6(SDF4):c.499G>A (p.Glu167Lys)not specified [RCV004666946]uncertain significance112233011223301Humanname
407462065CV3480351single nucleotide variantNM_016176.6(SDF4):c.724G>A (p.Gly242Ser)not specified [RCV004658935]uncertain significance112186251218625Humanname
597713053CV3595091single nucleotide variantNM_016176.6(SDF4):c.325C>T (p.Arg109Trp)not specified [RCV004861234]uncertain significance112239491223949Humanname
597713076CV3595093single nucleotide variantNM_016176.6(SDF4):c.820G>A (p.Asp274Asn)not specified [RCV004861236]uncertain significance112185291218529Humanname
597713087CV3595094single nucleotide variantNM_016176.6(SDF4):c.809A>T (p.Asn270Ile)not specified [RCV004861237]uncertain significance112185401218540Humanname
597713096CV3595095single nucleotide variantNM_016176.6(SDF4):c.353G>A (p.Arg118His)not specified [RCV004861238]likely benign112239211223921Humanname
597713108CV3595096single nucleotide variantNM_016176.6(SDF4):c.551A>G (p.Glu184Gly)not specified [RCV004861239]uncertain significance112232491223249Humanname
598236555CV3906872single nucleotide variantNM_016176.6(SDF4):c.586C>T (p.Arg196Cys)not specified [RCV005275452]uncertain significance112188981218898Humanname
598236564CV3906874single nucleotide variantNM_016176.6(SDF4):c.988G>A (p.Glu330Lys)not specified [RCV005275454]uncertain significance112175921217592Humanname
598236569CV3906875single nucleotide variantNM_016176.6(SDF4):c.952G>T (p.Val318Phe)not specified [RCV005275455]uncertain significance112176281217628Humanname
156216931CV2348076single nucleotide variantNM_016176.6(SDF4):c.1018A>G (p.Thr340Ala)not specified [RCV004197757]uncertain significance112175621217562Humanname
155905911CV2393822single nucleotide variantNM_016176.6(SDF4):c.1043C>T (p.Ala348Val)not specified [RCV004233651]uncertain significance112175371217537Humanname