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14 records found for search term Hat1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597781223CV3682158single nucleotide variantNM_003642.4(HAT1):c.94G>A (p.Ala32Thr)not specified [RCV004930840]uncertain significance2171925623171925623Humanname
155924298CV2212710single nucleotide variantNM_003642.4(HAT1):c.383C>T (p.Ser128Phe)not specified [RCV004085215]uncertain significance2171965411171965411Humanname
156038745CV2260079single nucleotide variantNM_003642.4(HAT1):c.524A>G (p.His175Arg)not specified [RCV004119084]uncertain significance2171965821171965821Humanname
156000364CV2296301single nucleotide variantNM_003642.4(HAT1):c.450T>G (p.Ser150Arg)not specified [RCV004154200]uncertain significance2171965478171965478Humanname
156236213CV2346422single nucleotide variantNM_003642.4(HAT1):c.841A>T (p.Ser281Cys)not specified [RCV004203900]uncertain significance2171976174171976174Humanname
329363217CV2445979single nucleotide variantNM_003642.4(HAT1):c.483A>G (p.Ile161Met)not specified [RCV004270567]uncertain significance2171965511171965511Humanname
597709613CV3682159single nucleotide variantNM_003642.4(HAT1):c.691C>T (p.Pro231Ser)not specified [RCV004917338]uncertain significance2171966488171966488Humanname
597781230CV3682161single nucleotide variantNM_003642.4(HAT1):c.448A>G (p.Ser150Gly)not specified [RCV004930842]uncertain significance2171965476171965476Humanname
156102557CV2313593single nucleotide variantNM_003642.4(HAT1):c.1202G>C (p.Ser401Thr)not specified [RCV004157530]uncertain significance2171983294171983294Humanname
156146484CV2381788single nucleotide variantNM_003642.4(HAT1):c.1063A>G (p.Ile355Val)not specified [RCV004232237]uncertain significance2171979334171979334Humanname
405789255CV3270012single nucleotide variantNM_003642.4(HAT1):c.1052A>G (p.Tyr351Cys)not specified [RCV004399188]uncertain significance2171979323171979323Humanname
405789259CV3270013single nucleotide variantNM_003642.4(HAT1):c.1231C>T (p.Arg411Cys)not specified [RCV004399189]uncertain significance2171983323171983323Humanname
597781226CV3682160single nucleotide variantNM_003642.4(HAT1):c.1237A>G (p.Ile413Val)not specified [RCV004930841]uncertain significance2171983329171983329Humanname
598265476CV3971409single nucleotide variantNM_003642.4(HAT1):c.1028G>A (p.Ser343Asn)not specified [RCV005349066]uncertain significance2171979299171979299Humanname