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27 records found for search term Apof
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407524812CV3460735single nucleotide variantNM_001638.4(APOF):c.95A>T (p.His32Leu)not specified [RCV004653789]uncertain significance125636211156362111Humanname
597679808CV3569181single nucleotide variantNM_001638.4(APOF):c.76C>G (p.Leu26Val)not specified [RCV004837204]uncertain significance125636213056362130Humanname
8634794CV90014single nucleotide variantNM_001638.2(APOF):c.486C>T (p.Val162=)Malignant melanoma [RCV000070111]not provided125636172056361720Humanname
598269748CV3996111single nucleotide variantNM_001638.4(APOF):c.241C>T (p.Pro81Ser)not specified [RCV005388851]uncertain significance125636196556361965Humanname
156239284CV2193706single nucleotide variantNM_001638.4(APOF):c.442G>A (p.Ala148Thr)not specified [RCV004074300]uncertain significance125636176456361764Humanname
156166907CV2200966single nucleotide variantNM_001638.4(APOF):c.750G>T (p.Arg250Ser)not specified [RCV004074736]uncertain significance125636145656361456Humanname
156056478CV2243308single nucleotide variantNM_001638.4(APOF):c.961G>T (p.Ala321Ser)not specified [RCV004112008]uncertain significance125636124556361245Humanname
156212162CV2259932single nucleotide variantNM_001638.4(APOF):c.687G>C (p.Met229Ile)not specified [RCV004118959]uncertain significance125636151956361519Humanname
156055771CV2388700single nucleotide variantNM_001638.4(APOF):c.316G>A (p.Ala106Thr)not specified [RCV004239571]uncertain significance125636189056361890Humanname
329391038CV2451980single nucleotide variantNM_001638.4(APOF):c.550C>G (p.Gln184Glu)not specified [RCV004276935]uncertain significance125636165656361656Humanname
329372264CV2455133single nucleotide variantNM_001638.4(APOF):c.698C>T (p.Ser233Leu)not specified [RCV004272377]uncertain significance125636150856361508Humanname
329395956CV2463111single nucleotide variantNM_001638.4(APOF):c.397G>A (p.Gly133Ser)not specified [RCV004274912]uncertain significance125636180956361809Humanname
405662638CV3289891single nucleotide variantNM_001638.4(APOF):c.341A>G (p.Gln114Arg)not specified [RCV004417836]uncertain significance125636186556361865Humanname
405662641CV3289892single nucleotide variantNM_001638.4(APOF):c.414G>T (p.Arg138Ser)not specified [RCV004417837]uncertain significance125636179256361792Humanname
405662642CV3289893single nucleotide variantNM_001638.4(APOF):c.469C>G (p.Gln157Glu)not specified [RCV004417838]uncertain significance125636173756361737Humanname
405662649CV3289895single nucleotide variantNM_001638.4(APOF):c.496C>A (p.Leu166Ile)not specified [RCV004417840]uncertain significance125636171056361710Humanname
405662652CV3289896single nucleotide variantNM_001638.4(APOF):c.589A>G (p.Thr197Ala)not specified [RCV004417841]uncertain significance125636161756361617Humanname
405662654CV3289897single nucleotide variantNM_001638.4(APOF):c.796G>A (p.Ala266Thr)not specified [RCV004417842]uncertain significance125636141056361410Humanname
405662656CV3289898single nucleotide variantNM_001638.4(APOF):c.973G>A (p.Glu325Lys)not specified [RCV004417843]uncertain significance125636123356361233Humanname
407481220CV3460729single nucleotide variantNM_001638.4(APOF):c.363G>T (p.Gln121His)not specified [RCV004664550]uncertain significance125636184356361843Humanname
407524822CV3460740single nucleotide variantNM_001638.4(APOF):c.754G>A (p.Gly252Arg)not specified [RCV004653792]uncertain significance125636145256361452Humanname
407481271CV3460747single nucleotide variantNM_001638.4(APOF):c.623G>T (p.Gly208Val)not specified [RCV004664559]uncertain significance125636158356361583Humanname
597679799CV3569183single nucleotide variantNM_001638.4(APOF):c.773A>G (p.Gln258Arg)not specified [RCV004837205]uncertain significance125636143356361433Humanname
597679791CV3569186single nucleotide variantNM_001638.4(APOF):c.457G>T (p.Ala153Ser)not specified [RCV004837206]uncertain significance125636174956361749Humanname
597679783CV3569188single nucleotide variantNM_001638.4(APOF):c.919T>G (p.Trp307Gly)not specified [RCV004837207]uncertain significance125636128756361287Humanname
597679776CV3569193single nucleotide variantNM_001638.4(APOF):c.458C>T (p.Ala153Val)not specified [RCV004837208]uncertain significance125636174856361748Humanname
15111812CV713647single nucleotide variantNM_001638.4(APOF):c.338G>A (p.Arg113His)not provided [RCV000961180]benign125636186856361868Humanname