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29 records found for search term Teddm1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598164236CV3923994single nucleotide variantNM_172000.4(TEDDM1):c.23T>C (p.Leu8Pro)not specified [RCV005283257]uncertain significance1182400463182400463Humanname
407517944CV3482202single nucleotide variantNM_172000.4(TEDDM1):c.62C>G (p.Ala21Gly)not specified [RCV004675809]uncertain significance1182400424182400424Humanname
156159031CV2322705single nucleotide variantNM_172000.4(TEDDM1):c.260T>A (p.Met87Lys)not specified [RCV004182828]uncertain significance1182400226182400226Humanname
156006313CV2357762single nucleotide variantNM_172000.4(TEDDM1):c.161T>C (p.Leu54Pro)not specified [RCV004205055]uncertain significance1182400325182400325Humanname
405766350CV3328461single nucleotide variantNM_172000.4(TEDDM1):c.133G>A (p.Val45Ile)not specified [RCV004469515]likely benign1182400353182400353Humanname
598211193CV3923989single nucleotide variantNM_172000.4(TEDDM1):c.151G>A (p.Gly51Arg)not specified [RCV005291970]uncertain significance1182400335182400335Humanname
598164230CV3923993single nucleotide variantNM_172000.4(TEDDM1):c.158T>C (p.Val53Ala)not specified [RCV005283256]uncertain significance1182400328182400328Humanname
598164243CV3923995single nucleotide variantNM_172000.4(TEDDM1):c.263G>A (p.Ser88Asn)not specified [RCV005283258]uncertain significance1182400223182400223Humanname
156079053CV2248533single nucleotide variantNM_172000.4(TEDDM1):c.683G>T (p.Arg228Ile)not specified [RCV004119658]uncertain significance1182399803182399803Humanname
155918218CV2283504single nucleotide variantNM_172000.4(TEDDM1):c.588G>C (p.Met196Ile)not specified [RCV004139719]uncertain significance1182399898182399898Humanname
155997956CV2287093single nucleotide variantNM_172000.4(TEDDM1):c.721T>C (p.Tyr241His)not specified [RCV004144967]uncertain significance1182399765182399765Humanname
156177850CV2287882single nucleotide variantNM_172000.4(TEDDM1):c.667T>C (p.Trp223Arg)not specified [RCV004147669]uncertain significance1182399819182399819Humanname
156295561CV2297482single nucleotide variantNM_172000.4(TEDDM1):c.443T>G (p.Leu148Arg)not specified [RCV004153413]uncertain significance1182400043182400043Humanname
156349951CV2316112single nucleotide variantNM_172000.4(TEDDM1):c.607T>C (p.Cys203Arg)not specified [RCV004174164]uncertain significance1182399879182399879Humanname
156160721CV2323387single nucleotide variantNM_172000.4(TEDDM1):c.456C>A (p.Asn152Lys)not specified [RCV004171785]uncertain significance1182400030182400030Humanname
156197507CV2367327single nucleotide variantNM_172000.4(TEDDM1):c.725A>G (p.Tyr242Cys)not specified [RCV004208831]uncertain significance1182399761182399761Humanname
329369834CV2461242single nucleotide variantNM_172000.4(TEDDM1):c.409G>T (p.Val137Leu)not specified [RCV004267426]uncertain significance1182400077182400077Humanname
401726095CV2699082single nucleotide variantNM_172000.4(TEDDM1):c.802C>A (p.Leu268Ile)not specified [RCV004303594]uncertain significance1182399684182399684Humanname
405766358CV3328462single nucleotide variantNM_172000.4(TEDDM1):c.409G>A (p.Val137Met)not specified [RCV004469516]uncertain significance1182400077182400077Humanname
405766362CV3328463single nucleotide variantNM_172000.4(TEDDM1):c.523G>C (p.Gly175Arg)not specified [RCV004469517]uncertain significance1182399963182399963Humanname
405766373CV3328465single nucleotide variantNM_172000.4(TEDDM1):c.582C>A (p.Asp194Glu)not specified [RCV004469519]uncertain significance1182399904182399904Humanname
405766379CV3328466single nucleotide variantNM_172000.4(TEDDM1):c.770A>T (p.Glu257Val)not specified [RCV004469520]uncertain significance1182399716182399716Humanname
407519726CV3482203single nucleotide variantNM_172000.4(TEDDM1):c.313G>T (p.Val105Phe)not specified [RCV004676666]uncertain significance1182400173182400173Humanname
597773976CV3612831single nucleotide variantNM_172000.4(TEDDM1):c.433A>C (p.Thr145Pro)not specified [RCV004872183]uncertain significance1182400053182400053Humanname
597773980CV3612832single nucleotide variantNM_172000.4(TEDDM1):c.530T>A (p.Ile177Asn)not specified [RCV004872184]uncertain significance1182399956182399956Humanname
598211200CV3923990single nucleotide variantNM_172000.4(TEDDM1):c.389A>G (p.Tyr130Cys)not specified [RCV005291971]uncertain significance1182400097182400097Humanname
598211206CV3923991single nucleotide variantNM_172000.4(TEDDM1):c.706C>T (p.Pro236Ser)not specified [RCV005291972]likely benign1182399780182399780Humanname
598211214CV3923992single nucleotide variantNM_172000.4(TEDDM1):c.515T>C (p.Met172Thr)not specified [RCV005291973]uncertain significance1182399971182399971Humanname
8629140CV84285single nucleotide variantNM_172000.3(TEDDM1):c.712G>A (p.Glu238Lys)Malignant melanoma [RCV000064367]not provided1182399774182399774Humanname