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Variants search result for Homo sapiens
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12 records found for search term Tial1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156338227CV2224908single nucleotide variantNM_003252.4(TIAL1):c.130-48C>Tnot specified [RCV004092985]uncertain significance10119582605119582605Humanname
597795118CV3613255single nucleotide variantNM_003252.4(TIAL1):c.250A>G (p.Thr84Ala)not specified [RCV004878081]uncertain significance10119582202119582202Humanname
156054481CV2308673single nucleotide variantNM_003252.4(TIAL1):c.873T>G (p.Ser291Arg)not specified [RCV004167221]uncertain significance10119576739119576739Humanname
156357751CV2318357single nucleotide variantNM_003252.4(TIAL1):c.775T>G (p.Ser259Ala)not specified [RCV004179519]uncertain significance10119577166119577166Humanname
405751263CV3335718single nucleotide variantNM_003252.4(TIAL1):c.791C>T (p.Thr264Met)not specified [RCV004467136]uncertain significance10119577150119577150Humanname
407520228CV3479067single nucleotide variantNM_003252.4(TIAL1):c.563C>T (p.Thr188Ile)not specified [RCV004676884]uncertain significance10119577730119577730Humanname
597763800CV3613254single nucleotide variantNM_003252.4(TIAL1):c.842T>C (p.Met281Thr)not specified [RCV004869947]uncertain significance10119577099119577099Humanname
598185754CV3913722single nucleotide variantNM_003252.4(TIAL1):c.841A>G (p.Met281Val)not specified [RCV005287485]uncertain significance10119577100119577100Humanname
598185760CV3913723single nucleotide variantNM_003252.4(TIAL1):c.833C>G (p.Ser278Cys)not specified [RCV005287486]uncertain significance10119577108119577108Humanname
598185766CV3913724single nucleotide variantNM_003252.4(TIAL1):c.806T>C (p.Val269Ala)not specified [RCV005287487]uncertain significance10119577135119577135Humanname
156129456CV2279678single nucleotide variantNM_003252.4(TIAL1):c.1066C>T (p.Pro356Ser)not specified [RCV004144301]uncertain significance10119575727119575727Humanname
597763796CV3613253single nucleotide variantNM_003252.4(TIAL1):c.1009C>T (p.Pro337Ser)not specified [RCV004869946]uncertain significance10119575784119575784Humanname