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36 records found for search term Stbd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329361905CV2468435single nucleotide variantNM_003943.5(STBD1):c.4G>A (p.Gly2Ser)not specified [RCV004277742]uncertain significance47630677376306773Humanname
156072221CV2240407single nucleotide variantNM_003943.5(STBD1):c.15G>C (p.Trp5Cys)not specified [RCV004117302]uncertain significance47630678476306784Humanname
156397395CV2200423single nucleotide variantNM_003943.5(STBD1):c.71G>C (p.Arg24Pro)not specified [RCV004076741]uncertain significance47630684076306840Humanname
405739896CV3334334single nucleotide variantNM_003943.5(STBD1):c.52C>A (p.Leu18Ile)not specified [RCV004465547]uncertain significance47630682176306821Humanname
407486558CV3485415single nucleotide variantNM_003943.5(STBD1):c.44C>T (p.Ala15Val)not specified [RCV004668043]uncertain significance47630681376306813Humanname
407486566CV3485416single nucleotide variantNM_003943.5(STBD1):c.70C>T (p.Arg24Trp)not specified [RCV004668044]uncertain significance47630683976306839Humanname
156081412CV2249058single nucleotide variantNM_003943.5(STBD1):c.239A>G (p.Asn80Ser)not specified [RCV004116336]uncertain significance47630916276309162Humanname
156153877CV2266033single nucleotide variantNM_003943.5(STBD1):c.154G>T (p.Gly52Cys)not specified [RCV004126852]uncertain significance47630692376306923Humanname
329370568CV2461765single nucleotide variantNM_003943.5(STBD1):c.290C>T (p.Ser97Leu)not specified [RCV004269910]uncertain significance47630921376309213Humanname
405740414CV3334331single nucleotide variantNM_003943.5(STBD1):c.101G>C (p.Gly34Ala)not specified [RCV004465544]uncertain significance47630687076306870Humanname
405739880CV3334332single nucleotide variantNM_003943.5(STBD1):c.284C>T (p.Ala95Val)not specified [RCV004465545]uncertain significance47630920776309207Humanname
407486572CV3485417single nucleotide variantNM_003943.5(STBD1):c.161A>G (p.Gln54Arg)not specified [RCV004668045]uncertain significance47630693076306930Humanname
598251161CV3919548single nucleotide variantNM_003943.5(STBD1):c.130C>T (p.Leu44Phe)not specified [RCV005277834]uncertain significance47630689976306899Humanname
156080354CV2198462single nucleotide variantNM_003943.5(STBD1):c.763G>A (p.Ala255Thr)not specified [RCV004081988]uncertain significance47630968676309686Humanname
156333667CV2220867single nucleotide variantNM_003943.5(STBD1):c.335G>A (p.Arg112Lys)not specified [RCV004092295]uncertain significance47630925876309258Humanname
156084610CV2249274single nucleotide variantNM_003943.5(STBD1):c.341A>G (p.His114Arg)not specified [RCV004118303]uncertain significance47630926476309264Humanname
156360097CV2254205single nucleotide variantNM_003943.5(STBD1):c.790G>C (p.Val264Leu)not specified [RCV004129884]uncertain significance47630971376309713Humanname
156024386CV2273863single nucleotide variantNM_003943.5(STBD1):c.365A>G (p.Asp122Gly)not specified [RCV004132488]uncertain significance47630928876309288Humanname
156101960CV2291436single nucleotide variantNM_003943.5(STBD1):c.880A>G (p.Asn294Asp)not specified [RCV004155765]uncertain significance47630980376309803Humanname
156269723CV2293325single nucleotide variantNM_003943.5(STBD1):c.538A>C (p.Lys180Gln)not specified [RCV004150809]uncertain significance47630946176309461Humanname
156282565CV2363137single nucleotide variantNM_003943.5(STBD1):c.532C>G (p.Leu178Val)not specified [RCV004211260]uncertain significance47630945576309455Humanname
155958794CV2390421single nucleotide variantNM_003943.5(STBD1):c.590G>A (p.Arg197Gln)not specified [RCV004238967]uncertain significance47630951376309513Humanname
329353299CV2469119single nucleotide variantNM_003943.5(STBD1):c.356A>G (p.Gln119Arg)not specified [RCV004274349]uncertain significance47630927976309279Humanname
401738618CV2721930single nucleotide variantNM_003943.5(STBD1):c.586G>T (p.Asp196Tyr)not specified [RCV004326429]uncertain significance47630950976309509Humanname
401872175CV2793002single nucleotide variantNM_003943.5(STBD1):c.971T>C (p.Val324Ala)not specified [RCV004360340]uncertain significance47630989476309894Humanname
405739890CV3334333single nucleotide variantNM_003943.5(STBD1):c.500C>A (p.Thr167Lys)not specified [RCV004465546]uncertain significance47630942376309423Humanname
405739905CV3334335single nucleotide variantNM_003943.5(STBD1):c.708A>C (p.Arg236Ser)not specified [RCV004465548]uncertain significance47630963176309631Humanname
597747215CV3618559single nucleotide variantNM_003943.5(STBD1):c.649G>A (p.Val217Met)not specified [RCV004866022]uncertain significance47630957276309572Humanname
597747220CV3618560single nucleotide variantNM_003943.5(STBD1):c.961T>C (p.Trp321Arg)not specified [RCV004866023]uncertain significance47630988476309884Humanname
597703571CV3618561single nucleotide variantNM_003943.5(STBD1):c.662T>C (p.Leu221Pro)not specified [RCV004860207]uncertain significance47630958576309585Humanname
597703581CV3618562single nucleotide variantNM_003943.5(STBD1):c.724G>T (p.Ala242Ser)not specified [RCV004860208]uncertain significance47630964776309647Humanname
598251166CV3919549single nucleotide variantNM_003943.5(STBD1):c.600C>G (p.His200Gln)not specified [RCV005277835]uncertain significance47630952376309523Humanname
156330207CV2210571single nucleotide variantNM_003943.5(STBD1):c.1057G>A (p.Ala353Thr)not specified [RCV004083726]uncertain significance47630998076309980Humanname
156245272CV2283413single nucleotide variantNM_003943.5(STBD1):c.1025T>C (p.Leu342Pro)not specified [RCV004139640]uncertain significance47630994876309948Humanname
156270525CV2315552single nucleotide variantNM_003943.5(STBD1):c.1060T>C (p.Trp354Arg)not specified [RCV004169598]uncertain significance47630998376309983Humanname
156244323CV2347140single nucleotide variantNM_003943.5(STBD1):c.1063T>C (p.Trp355Arg)not specified [RCV004204617]uncertain significance47630998676309986Humanname