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74 records found for search term Ifrd2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156267878CV2314645single nucleotide variantNM_006764.5(IFRD2):c.-39G>Anot specified [RCV004170802]uncertain significance35029231350292313Humanname
156198512CV2357874single nucleotide variantNM_006764.5(IFRD2):c.-26C>Tnot specified [RCV004205154]uncertain significance35029230050292300Humanname
329372420CV2443027single nucleotide variantNM_006764.5(IFRD2):c.-11C>Gnot specified [RCV004253617]uncertain significance35029228550292285Humanname
405792581CV3263770single nucleotide variantNM_006764.5(IFRD2):c.-92T>Cnot specified [RCV004400240]uncertain significance35029236650292366Humanname
407466453CV3440633single nucleotide variantNM_006764.5(IFRD2):c.-42A>Gnot specified [RCV004635634]likely benign35029231650292316Humanname
597763768CV3679905single nucleotide variantNM_006764.5(IFRD2):c.-27C>Tnot specified [RCV004926444]uncertain significance35029230150292301Humanname
156064027CV2200052single nucleotide variantNM_006764.5(IFRD2):c.-123C>Anot specified [RCV004074206]uncertain significance35029239750292397Humanname
156156956CV2266253single nucleotide variantNM_006764.5(IFRD2):c.-141C>Anot specified [RCV004128815]uncertain significance35029241550292415Humanname
155943922CV2294913single nucleotide variantNM_006764.5(IFRD2):c.-138G>Anot specified [RCV004156063]uncertain significance35029241250292412Humanname
405792600CV3263776single nucleotide variantNM_006764.5(IFRD2):c.-122G>Tnot specified [RCV004400246]uncertain significance35029239650292396Humanname
597763748CV3679899single nucleotide variantNM_006764.5(IFRD2):c.-108C>Tnot specified [RCV004926438]uncertain significance35029238250292382Humanname
598206670CV3979297single nucleotide variantNM_006764.5(IFRD2):c.-107C>Gnot specified [RCV005337828]uncertain significance35029238150292381Humanname
156022023CV2223079single nucleotide variantNM_006764.5(IFRD2):c.5C>G (p.Pro2Arg)not specified [RCV004103934]uncertain significance35029227050292270Humanname
597695390CV3679908single nucleotide variantNM_006764.4(IFRD2):c.7T>G (p.Trp3Gly)not specified [RCV004926447]likely benign35029246050292460Humanname
597763752CV3679900single nucleotide variantNM_006764.5(IFRD2):c.13C>T (p.Arg5Cys)not specified [RCV004926439]uncertain significance35029226250292262Humanname
597695367CV3679904single nucleotide variantNM_006764.4(IFRD2):c.23G>A (p.Arg8Gln)not specified [RCV004926443]likely benign35029244450292444Humanname
150547311CV1291972single nucleotide variantNM_006764.5(IFRD2):c.47G>A (p.Arg16His)not provided [RCV004692716]|not specified [RCV001733638]uncertain significance35029222850292228Humanname
155991022CV2276538single nucleotide variantNM_006764.5(IFRD2):c.65G>A (p.Arg22Gln)not specified [RCV004144248]likely benign35029067350290673Humanname
405792587CV3263772single nucleotide variantNM_006764.5(IFRD2):c.38G>A (p.Gly13Asp)not specified [RCV004400242]uncertain significance35029223750292237Humanname
597695377CV3679906single nucleotide variantNM_006764.4(IFRD2):c.36G>T (p.Trp12Cys)not specified [RCV004926445]uncertain significance35029243150292431Humanname
156258511CV2204665single nucleotide variantNM_006764.5(IFRD2):c.179G>C (p.Gly60Ala)not specified [RCV004081769]uncertain significance35029047250290472Humanname
401735634CV2695363single nucleotide variantNM_006764.5(IFRD2):c.122G>A (p.Arg41His)not specified [RCV004305574]uncertain significance35029061650290616Humanname
401860568CV2776100single nucleotide variantNM_006764.5(IFRD2):c.147C>G (p.Ser49Arg)not specified [RCV004353203]uncertain significance35029059150290591Humanname
405792593CV3263774single nucleotide variantNM_006764.5(IFRD2):c.115G>A (p.Glu39Lys)not specified [RCV004400244]uncertain significance35029062350290623Humanname
405792596CV3263775single nucleotide variantNM_006764.5(IFRD2):c.253A>G (p.Thr85Ala)not specified [RCV004400245]uncertain significance35029039850290398Humanname
407466461CV3440635single nucleotide variantNM_006764.5(IFRD2):c.274C>T (p.Arg92Trp)not specified [RCV004635636]uncertain significance35029028450290284Humanname
407466470CV3440637single nucleotide variantNM_006764.5(IFRD2):c.181G>A (p.Gly61Arg)not specified [RCV004635638]uncertain significance35029047050290470Humanname
598268384CV3979295single nucleotide variantNM_006764.5(IFRD2):c.130G>A (p.Ala44Thr)not specified [RCV005349691]likely benign35029060850290608Humanname
598268405CV3979300single nucleotide variantNM_006764.5(IFRD2):c.275G>A (p.Arg92Gln)not specified [RCV005349695]uncertain significance35029028350290283Humanname
15175724CV698184single nucleotide variantNM_006764.5(IFRD2):c.237G>C (p.Glu79Asp)not provided [RCV000950656]benign35029041450290414Humanname
156268120CV2198878single nucleotide variantNM_006764.5(IFRD2):c.641G>A (p.Arg214Gln)not specified [RCV004077913]uncertain significance35028958550289585Humanname
156032546CV2214471single nucleotide variantNM_006764.5(IFRD2):c.690C>G (p.Ser230Arg)not specified [RCV004088528]uncertain significance35028953650289536Humanname
156150746CV2235079single nucleotide variantNM_006764.5(IFRD2):c.311C>T (p.Ala104Val)not specified [RCV004113258]uncertain significance35029024750290247Humanname
156098158CV2306438single nucleotide variantNM_006764.5(IFRD2):c.347G>A (p.Arg116His)not specified [RCV004157064]uncertain significance35029021150290211Humanname
156242863CV2306649single nucleotide variantNM_006764.5(IFRD2):c.671G>T (p.Ser224Ile)not specified [RCV004157246]uncertain significance35028955550289555Humanname
156055277CV2320523single nucleotide variantNM_006764.5(IFRD2):c.955A>G (p.Lys319Glu)not specified [RCV004172153]uncertain significance35028886850288868Humanname
156087645CV2366411single nucleotide variantNM_006764.5(IFRD2):c.346C>T (p.Arg116Cys)not specified [RCV004212456]uncertain significance35029021250290212Humanname
156257112CV2397839single nucleotide variantNM_006764.5(IFRD2):c.835G>A (p.Ala279Thr)not specified [RCV004239309]uncertain significance35028930550289305Humanname
401770720CV2685859single nucleotide variantNM_006764.5(IFRD2):c.980G>A (p.Arg327Gln)not specified [RCV004294843]uncertain significance35028884350288843Humanname
401729328CV2732967single nucleotide variantNM_006764.5(IFRD2):c.879C>A (p.Asp293Glu)not specified [RCV004331143]uncertain significance35028926150289261Humanname
401889908CV2755396single nucleotide variantNM_006764.5(IFRD2):c.427G>A (p.Gly143Ser)not specified [RCV004337558]uncertain significance35029004850290048Humanname
401887533CV2771996single nucleotide variantNM_006764.5(IFRD2):c.790C>T (p.Arg264Trp)not specified [RCV004344678]uncertain significance35028935050289350Humanname
401869576CV2772449single nucleotide variantNM_006764.5(IFRD2):c.644T>A (p.Phe215Tyr)not specified [RCV004355233]uncertain significance35028958250289582Humanname
401898406CV2787868single nucleotide variantNM_006764.5(IFRD2):c.697G>A (p.Gly233Ser)not specified [RCV004358546]uncertain significance35028952950289529Humanname
405792584CV3263771single nucleotide variantNM_006764.5(IFRD2):c.898T>C (p.Tyr300His)not specified [RCV004400241]uncertain significance35028892550288925Humanname
405792603CV3263777single nucleotide variantNM_006764.5(IFRD2):c.532G>T (p.Ala178Ser)not specified [RCV004400247]uncertain significance35028994350289943Humanname
405792606CV3263778single nucleotide variantNM_006764.5(IFRD2):c.577G>C (p.Val193Leu)not specified [RCV004400248]uncertain significance35028973250289732Humanname
405792609CV3263779single nucleotide variantNM_006764.5(IFRD2):c.640C>T (p.Arg214Trp)not specified [RCV004400249]uncertain significance35028958650289586Humanname
407466449CV3440631single nucleotide variantNM_006764.5(IFRD2):c.901G>A (p.Glu301Lys)not specified [RCV004635633]uncertain significance35028892250288922Humanname
407466465CV3440636single nucleotide variantNM_006764.5(IFRD2):c.759A>T (p.Gln253His)not specified [RCV004635637]likely benign35028946750289467Humanname
597763761CV3679902single nucleotide variantNM_006764.5(IFRD2):c.656G>C (p.Gly219Ala)not specified [RCV004926441]uncertain significance35028957050289570Humanname
597763765CV3679903single nucleotide variantNM_006764.5(IFRD2):c.830G>A (p.Arg277Gln)not specified [RCV004926442]uncertain significance35028931050289310Humanname
597763776CV3679909single nucleotide variantNM_006764.5(IFRD2):c.932G>A (p.Arg311His)not specified [RCV004926448]uncertain significance35028889150288891Humanname
597763779CV3679910single nucleotide variantNM_006764.5(IFRD2):c.923G>C (p.Ser308Thr)not specified [RCV004926449]uncertain significance35028890050288900Humanname
598268389CV3979296single nucleotide variantNM_006764.5(IFRD2):c.361G>A (p.Asp121Asn)not specified [RCV005349692]uncertain significance35029019750290197Humanname
598268399CV3979299single nucleotide variantNM_006764.5(IFRD2):c.931C>T (p.Arg311Cys)not specified [RCV005349694]uncertain significance35028889250288892Humanname
598268410CV3979301single nucleotide variantNM_006764.5(IFRD2):c.344G>A (p.Arg115His)not specified [RCV005349696]uncertain significance35029021450290214Humanname
598268416CV3979302single nucleotide variantNM_006764.5(IFRD2):c.536C>T (p.Ala179Val)not specified [RCV005349697]uncertain significance35028993950289939Humanname
156160409CV2262663single nucleotide variantNM_006764.5(IFRD2):c.1213G>T (p.Ala405Ser)not specified [RCV004130858]uncertain significance35028844450288444Humanname
156048164CV2315747single nucleotide variantNM_006764.5(IFRD2):c.1174A>G (p.Ile392Val)not specified [RCV004169756]uncertain significance35028848350288483Humanname
329400012CV2444357single nucleotide variantNM_006764.5(IFRD2):c.1057G>A (p.Gly353Ser)not specified [RCV004263108]uncertain significance35028867850288678Humanname
329358861CV2454341single nucleotide variantNM_006764.5(IFRD2):c.1238G>T (p.Arg413Leu)not specified [RCV004265794]uncertain significance35028841950288419Humanname
401729562CV2690336single nucleotide variantNM_006764.5(IFRD2):c.1156A>G (p.Asn386Asp)not specified [RCV004302332]uncertain significance35028850150288501Humanname
401888492CV2761545single nucleotide variantNM_006764.5(IFRD2):c.1166T>C (p.Leu389Pro)not specified [RCV004334714]uncertain significance35028849150288491Humanname
401879176CV2778222single nucleotide variantNM_006764.5(IFRD2):c.1303C>T (p.Arg435Trp)not specified [RCV004349942]uncertain significance35028821750288217Humanname
407466437CV3440628single nucleotide variantNM_006764.5(IFRD2):c.1130C>T (p.Ser377Leu)not specified [RCV004635630]uncertain significance35028860550288605Humanname
407466441CV3440629single nucleotide variantNM_006764.5(IFRD2):c.1080C>A (p.Asp360Glu)not specified [RCV004635631]uncertain significance35028865550288655Humanname
407466445CV3440630single nucleotide variantNM_006764.5(IFRD2):c.1165C>T (p.Leu389Phe)not specified [RCV004635632]uncertain significance35028849250288492Humanname
407511075CV3440632single nucleotide variantNM_006764.5(IFRD2):c.1298G>A (p.Arg433His)not specified [RCV004626344]uncertain significance35028822250288222Humanname
407466457CV3440634single nucleotide variantNM_006764.5(IFRD2):c.1076T>C (p.Met359Thr)not specified [RCV004635635]uncertain significance35028865950288659Humanname
597763744CV3679898single nucleotide variantNM_006764.5(IFRD2):c.1075A>G (p.Met359Val)not specified [RCV004926437]likely benign35028866050288660Humanname
597763772CV3679907single nucleotide variantNM_006764.5(IFRD2):c.1096C>T (p.Arg366Trp)not specified [RCV004926446]uncertain significance35028863950288639Humanname
598206664CV3979294single nucleotide variantNM_006764.5(IFRD2):c.1006G>A (p.Val336Met)not specified [RCV005337827]uncertain significance35028881750288817Humanname
598268394CV3979298single nucleotide variantNM_006764.5(IFRD2):c.1262C>T (p.Ala421Val)not specified [RCV005349693]uncertain significance35028825850288258Humanname