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Variants search result for Homo sapiens
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12 records found for search term Tcte1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407451316CV3485974single nucleotide variantNM_182539.4(TCTE1):c.185G>A (p.Arg62His)not specified [RCV004675682]uncertain significance64428764144287641Humanname
597773017CV3615967single nucleotide variantNM_182539.4(TCTE1):c.902G>A (p.Arg301Gln)not specified [RCV004871970]uncertain significance64428250444282504Humanname
597773032CV3615970single nucleotide variantNM_182539.4(TCTE1):c.446G>A (p.Gly149Asp)not specified [RCV004871973]uncertain significance64428636444286364Humanname
597773038CV3615971single nucleotide variantNM_182539.4(TCTE1):c.899T>A (p.Ile300Asn)not specified [RCV004871974]uncertain significance64428250744282507Humanname
407451320CV3485975single nucleotide variantNM_182539.4(TCTE1):c.1174C>T (p.Leu392Phe)not specified [RCV004675683]uncertain significance64428223244282232Humanname
407451325CV3485976single nucleotide variantNM_182539.4(TCTE1):c.1262C>A (p.Thr421Asn)not specified [RCV004675684]uncertain significance64428214444282144Humanname
597773027CV3615969single nucleotide variantNM_182539.4(TCTE1):c.1004G>A (p.Arg335His)not specified [RCV004871972]uncertain significance64428240244282402Humanname
597773043CV3615972single nucleotide variantNM_182539.4(TCTE1):c.1090C>T (p.Leu364Phe)not specified [RCV004871975]uncertain significance64428231644282316Humanname
8626218CV81362single nucleotide variantNM_182539.3(TCTE1):c.1451C>T (p.Pro484Leu)Malignant melanoma [RCV000061440]not provided64428023644280236Humanname
8626219CV81363single nucleotide variantNM_182539.3(TCTE1):c.1097C>T (p.Ser366Phe)Malignant melanoma [RCV000061441]not provided64428230944282309Humanname
405280143CV3206502single nucleotide variantNM_182539.4(DRC5):c.547C>T (p.Leu183Phe)TCTE1-related disorder [RCV003981214]likely benign64428626344286263Humantrait , alternate_id
405275077CV3214862single nucleotide variantNM_182539.4(DRC5):c.928G>A (p.Glu310Lys)TCTE1-related disorder [RCV003934269]likely benign64428247844282478Humantrait , alternate_id