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44 records found for search term Epyc
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15119096CV744940single nucleotide variantNM_004950.5(EPYC):c.702+1G>Cnot provided [RCV000895663]likely benign129097179990971799Humanname
15160408CV778133deletionNM_004950.5(EPYC):c.166-4delnot provided [RCV000947478]benign129097826690978266Humanname
155982353CV2351596single nucleotide variantNM_004950.5(EPYC):c.4A>C (p.Lys2Gln)not specified [RCV004195313]uncertain significance129100256291002562Humanname
401763469CV2714564single nucleotide variantNM_004950.5(EPYC):c.23T>C (p.Val8Ala)not specified [RCV004318076]uncertain significance129100254391002543Humanname
155943762CV2241742single nucleotide variantNM_004950.5(EPYC):c.35T>A (p.Val12Asp)not specified [RCV004106682]uncertain significance129100253191002531Humanname
405740754CV3249351single nucleotide variantNM_004950.5(EPYC):c.31C>T (p.Leu11Phe)not specified [RCV004380430]uncertain significance129100253591002535Humanname
405740012CV3249355single nucleotide variantNM_004950.5(EPYC):c.46G>A (p.Ala16Thr)not specified [RCV004380434]uncertain significance129100252091002520Humanname
405740022CV3249356single nucleotide variantNM_004950.5(EPYC):c.47C>A (p.Ala16Asp)not specified [RCV004380435]uncertain significance129100251991002519Humanname
156335777CV2228438single nucleotide variantNM_004950.5(EPYC):c.240G>C (p.Gln80His)not specified [RCV004098410]uncertain significance129097818890978188Humanname
155995115CV2250312single nucleotide variantNM_004950.5(EPYC):c.125A>G (p.Asn42Ser)not specified [RCV004127209]uncertain significance129100244191002441Humanname
155982048CV2337120single nucleotide variantNM_004950.5(EPYC):c.152T>C (p.Val51Ala)not specified [RCV004192880]uncertain significance129100241491002414Humanname
156239690CV2356366single nucleotide variantNM_004950.5(EPYC):c.149C>A (p.Pro50His)not specified [RCV004206169]uncertain significance129100241791002417Humanname
401872740CV2779984single nucleotide variantNM_004950.5(EPYC):c.254A>C (p.Glu85Ala)not specified [RCV004353575]uncertain significance129097817490978174Humanname
405740763CV3249350single nucleotide variantNM_004950.5(EPYC):c.103G>C (p.Ala35Pro)not specified [RCV004380429]uncertain significance129100246391002463Humanname
407479474CV3441907single nucleotide variantNM_004950.5(EPYC):c.268C>G (p.Pro90Ala)not specified [RCV004617783]uncertain significance129097816090978160Humanname
597748222CV3671394single nucleotide variantNM_004950.5(EPYC):c.287C>G (p.Ser96Cys)not specified [RCV004923055]uncertain significance129097814190978141Humanname
156146586CV2212767single nucleotide variantNM_004950.5(EPYC):c.410C>T (p.Ala137Val)not specified [RCV004091460]uncertain significance129097291190972911Humanname
156315499CV2250776single nucleotide variantNM_004950.5(EPYC):c.706A>T (p.Met236Leu)not specified [RCV004129645]uncertain significance129097013690970136Humanname
156188304CV2292533single nucleotide variantNM_004950.5(EPYC):c.706A>G (p.Met236Val)not specified [RCV004150307]uncertain significance129097013690970136Humanname
156087200CV2295401single nucleotide variantNM_004950.5(EPYC):c.902T>C (p.Ile301Thr)not specified [RCV004158744]uncertain significance129096422390964223Humanname
156014889CV2301623single nucleotide variantNM_004950.5(EPYC):c.362G>A (p.Cys121Tyr)not specified [RCV004162528]uncertain significance129097295990972959Humanname
156201012CV2313115single nucleotide variantNM_004950.5(EPYC):c.749A>C (p.Asp250Ala)not specified [RCV004161384]uncertain significance129097009390970093Humanname
156272545CV2323360single nucleotide variantNM_004950.5(EPYC):c.913A>G (p.Lys305Glu)not specified [RCV004171763]uncertain significance129096421290964212Humanname
156179132CV2327638single nucleotide variantNM_004950.5(EPYC):c.386A>G (p.Tyr129Cys)not specified [RCV004177221]uncertain significance129097293590972935Humanname
156215042CV2347811single nucleotide variantNM_004950.5(EPYC):c.852G>C (p.Leu284Phe)not specified [RCV004195467]uncertain significance129096427390964273Humanname
156175716CV2355713single nucleotide variantNM_004950.5(EPYC):c.656G>A (p.Ser219Asn)not specified [RCV004199075]uncertain significance129097184690971846Humanname
156149271CV2359478single nucleotide variantNM_004950.5(EPYC):c.425C>T (p.Pro142Leu)not specified [RCV004214792]uncertain significance129097289690972896Humanname
156260342CV2381129single nucleotide variantNM_004950.5(EPYC):c.863G>A (p.Arg288His)not specified [RCV004225159]uncertain significance129096426290964262Humanname
329358999CV2425321single nucleotide variantNM_004950.5(EPYC):c.595C>T (p.Arg199Cys)not specified [RCV004250986]uncertain significance129097190790971907Humanname
329353986CV2436730single nucleotide variantNM_004950.5(EPYC):c.943C>T (p.Arg315Cys)not specified [RCV004258098]uncertain significance129096418290964182Humanname
401762023CV2713984single nucleotide variantNM_004950.5(EPYC):c.960C>A (p.Ser320Arg)not specified [RCV004315396]uncertain significance129096416590964165Humanname
401874036CV2757807single nucleotide variantNM_004950.5(EPYC):c.822C>G (p.His274Gln)not specified [RCV004336954]uncertain significance129096430390964303Humanname
401898990CV2785920single nucleotide variantNM_004950.5(EPYC):c.336T>A (p.Asn112Lys)not specified [RCV004365435]uncertain significance129097809290978092Humanname
405740520CV3249352single nucleotide variantNM_004950.5(EPYC):c.342C>G (p.Asp114Glu)not specified [RCV004380431]uncertain significance129097297990972979Humanname
405740325CV3249353single nucleotide variantNM_004950.5(EPYC):c.382G>A (p.Val128Met)not specified [RCV004380432]uncertain significance129097293990972939Humanname
405740026CV3249357single nucleotide variantNM_004950.5(EPYC):c.596G>A (p.Arg199His)not specified [RCV004380436]uncertain significance129097190690971906Humanname
407479459CV3441903single nucleotide variantNM_004950.5(EPYC):c.581G>A (p.Arg194Gln)not specified [RCV004617779]uncertain significance129097192190971921Humanname
407479465CV3441905single nucleotide variantNM_004950.5(EPYC):c.652A>G (p.Ile218Val)not specified [RCV004617781]uncertain significance129097185090971850Humanname
407479469CV3441906single nucleotide variantNM_004950.5(EPYC):c.880A>G (p.Ile294Val)not specified [RCV004617782]uncertain significance129096424590964245Humanname
597804085CV3671390single nucleotide variantNM_004950.5(EPYC):c.419C>T (p.Pro140Leu)not specified [RCV004907516]uncertain significance129097290290972902Humanname
597804087CV3671391single nucleotide variantNM_004950.5(EPYC):c.656G>C (p.Ser219Thr)not specified [RCV004907517]uncertain significance129097184690971846Humanname
597804091CV3671393single nucleotide variantNM_004950.5(EPYC):c.538T>C (p.Ser180Pro)not specified [RCV004907519]uncertain significance129097196490971964Humanname
15200845CV725313single nucleotide variantNM_004950.5(EPYC):c.562C>T (p.Arg188Ter)not provided [RCV000891024]likely benign129097194090971940Humanname
8627395CV82539single nucleotide variantNM_004950.4(EPYC):c.823G>A (p.Glu275Lys)Malignant melanoma [RCV000062618]not provided129096430290964302Humanname