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15 records found for search term Nkx6-3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15118197CV779287single nucleotide variantNM_001364841.2(NKX6-3):c.553-7A>Tnot provided [RCV000962333]benign84164670141646701Humanname
405707180CV3362311single nucleotide variantNM_001364841.2(NKX6-3):c.553-585C>Tnot specified [RCV004493299]uncertain significance84164727941647279Humanname
407497557CV3458666single nucleotide variantNM_001364841.2(NKX6-3):c.553-619G>Anot specified [RCV004643778]uncertain significance84164731341647313Humanname
15118203CV711526single nucleotide variantNM_001364841.2(NKX6-3):c.553-589G>Tnot provided [RCV000962334]benign84164728341647283Humanname
155925286CV2258501single nucleotide variantNM_001364841.2(NKX6-3):c.662G>C (p.Arg221Pro)not specified [RCV004115993]uncertain significance84164658541646585Humanname
156179366CV2288003single nucleotide variantNM_001364841.2(NKX6-3):c.607T>A (p.Ser203Thr)not specified [RCV004147767]uncertain significance84164664041646640Humanname
156081771CV2301111single nucleotide variantNM_001364841.2(NKX6-3):c.746G>T (p.Arg249Leu)not specified [RCV004160031]uncertain significance84164650141646501Humanname
155957737CV2304191single nucleotide variantNM_001364841.2(NKX6-3):c.752A>C (p.His251Pro)not specified [RCV004170215]uncertain significance84164649541646495Humanname
401880649CV2766203single nucleotide variantNM_001364841.2(NKX6-3):c.628C>A (p.Pro210Thr)not specified [RCV004340645]uncertain significance84164661941646619Humanname
407508912CV3458664single nucleotide variantNM_001364841.2(NKX6-3):c.755G>T (p.Arg252Leu)not specified [RCV004647269]uncertain significance84164649241646492Humanname
407508916CV3458665single nucleotide variantNM_001364841.2(NKX6-3):c.580T>C (p.Trp194Arg)not specified [RCV004647270]uncertain significance84164666741646667Humanname
597651438CV3556389single nucleotide variantNM_001364841.2(NKX6-3):c.778C>A (p.Leu260Met)not specified [RCV004826887]uncertain significance84164646941646469Humanname
597651445CV3556390single nucleotide variantNM_001364841.2(NKX6-3):c.631G>T (p.Gly211Cys)not specified [RCV004826888]uncertain significance84164661641646616Humanname
597651454CV3556391single nucleotide variantNM_001364841.2(NKX6-3):c.587A>G (p.Lys196Arg)not specified [RCV004826889]uncertain significance84164666041646660Humanname
597651466CV3556392single nucleotide variantNM_001364841.2(NKX6-3):c.692A>C (p.Tyr231Ser)not specified [RCV004826890]uncertain significance84164655541646555Humanname