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Variants search result for Homo sapiens
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48 records found for search term Fam91a1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15198165CV777675single nucleotide variantNM_144963.4(FAM91A1):c.1278+6T>Cnot provided [RCV000956671]benign8123787756123787756Humanname
597750938CV3675499single nucleotide variantNM_144963.4(FAM91A1):c.93A>T (p.Arg31Ser)not specified [RCV004923633]uncertain significance8123774100123774100Humanname
598238894CV3958614single nucleotide variantNM_144963.4(FAM91A1):c.95A>G (p.Glu32Gly)not specified [RCV005343887]uncertain significance8123774102123774102Humanname
156011626CV2362273single nucleotide variantNM_144963.4(FAM91A1):c.191A>G (p.Tyr64Cys)not specified [RCV004210062]uncertain significance8123775180123775180Humanname
401890590CV2778915single nucleotide variantNM_144963.4(FAM91A1):c.182G>A (p.Arg61His)not specified [RCV004346792]uncertain significance8123775171123775171Humanname
405761826CV3252915single nucleotide variantNM_144963.4(FAM91A1):c.128G>A (p.Arg43His)not specified [RCV004383631]uncertain significance8123774135123774135Humanname
405761836CV3252917single nucleotide variantNM_144963.4(FAM91A1):c.140G>A (p.Arg47Gln)not specified [RCV004383633]uncertain significance8123774147123774147Humanname
405761866CV3252922single nucleotide variantNM_144963.4(FAM91A1):c.275T>C (p.Ile92Thr)not specified [RCV004383638]uncertain significance8123775264123775264Humanname
597750906CV3675493single nucleotide variantNM_144963.4(FAM91A1):c.175G>T (p.Asp59Tyr)not specified [RCV004923627]uncertain significance8123775164123775164Humanname
597750922CV3675496single nucleotide variantNM_144963.4(FAM91A1):c.218A>T (p.Asp73Val)not specified [RCV004923630]uncertain significance8123775207123775207Humanname
156059409CV2343700single nucleotide variantNM_144963.4(FAM91A1):c.872G>A (p.Arg291Gln)not specified [RCV004190724]uncertain significance8123785651123785651Humanname
329398092CV2466691single nucleotide variantNM_144963.4(FAM91A1):c.606A>T (p.Gln202His)not specified [RCV004276197]uncertain significance8123780041123780041Humanname
401861148CV2758774single nucleotide variantNM_144963.4(FAM91A1):c.503C>T (p.Ala168Val)not specified [RCV004337831]uncertain significance8123778726123778726Humanname
405761872CV3252923single nucleotide variantNM_144963.4(FAM91A1):c.856G>A (p.Val286Ile)not specified [RCV004383639]uncertain significance8123785635123785635Humanname
597750901CV3675492single nucleotide variantNM_144963.4(FAM91A1):c.460C>G (p.Arg154Gly)not specified [RCV004923626]uncertain significance8123778683123778683Humanname
597750916CV3675495single nucleotide variantNM_144963.4(FAM91A1):c.841C>A (p.Leu281Met)not specified [RCV004923629]uncertain significance8123785111123785111Humanname
597750927CV3675497single nucleotide variantNM_144963.4(FAM91A1):c.556A>G (p.Thr186Ala)not specified [RCV004923631]uncertain significance8123779991123779991Humanname
597750949CV3675501single nucleotide variantNM_144963.4(FAM91A1):c.385A>C (p.Ile129Leu)not specified [RCV004923635]uncertain significance8123778042123778042Humanname
156370052CV2204100single nucleotide variantNM_144963.4(FAM91A1):c.1534C>T (p.Arg512Trp)not specified [RCV004076913]uncertain significance8123798212123798212Humanname
156069675CV2237145single nucleotide variantNM_144963.4(FAM91A1):c.1766C>T (p.Thr589Met)not specified [RCV004114893]uncertain significance8123799842123799842Humanname
155969129CV2244451single nucleotide variantNM_144963.4(FAM91A1):c.1010A>C (p.Glu337Ala)not specified [RCV004100416]uncertain significance8123786542123786542Humanname
156303574CV2258874single nucleotide variantNM_144963.4(FAM91A1):c.2167C>G (p.Leu723Val)not specified [RCV004118083]uncertain significance8123808922123808922Humanname
155973515CV2271649single nucleotide variantNM_144963.4(FAM91A1):c.1526A>G (p.Asn509Ser)not specified [RCV004130505]uncertain significance8123798204123798204Humanname
156063388CV2277422single nucleotide variantNM_144963.4(FAM91A1):c.1364A>G (p.Asn455Ser)not specified [RCV004144833]uncertain significance8123789698123789698Humanname
156037694CV2278861single nucleotide variantNM_144963.4(FAM91A1):c.1813C>T (p.His605Tyr)not specified [RCV004145568]uncertain significance8123805270123805270Humanname
155930563CV2296970single nucleotide variantNM_144963.4(FAM91A1):c.1697G>A (p.Ser566Asn)not specified [RCV004150902]uncertain significance8123799773123799773Humanname
156208053CV2298093single nucleotide variantNM_144963.4(FAM91A1):c.1706G>A (p.Arg569Gln)not specified [RCV004157980]uncertain significance8123799782123799782Humanname
156080121CV2351243single nucleotide variantNM_144963.4(FAM91A1):c.2213G>A (p.Arg738Gln)not specified [RCV004214090]likely benign8123808968123808968Humanname
155909772CV2359987single nucleotide variantNM_144963.4(FAM91A1):c.2017G>T (p.Ala673Ser)not specified [RCV004212828]uncertain significance8123806214123806214Humanname
401734627CV2688578single nucleotide variantNM_144963.4(FAM91A1):c.1289C>T (p.Thr430Ile)not specified [RCV004301535]uncertain significance8123789623123789623Humanname
401736805CV2699603single nucleotide variantNM_144963.4(FAM91A1):c.1423G>A (p.Asp475Asn)not specified [RCV004299792]uncertain significance8123798101123798101Humanname
401887432CV2771935single nucleotide variantNM_144963.4(FAM91A1):c.2233G>C (p.Ala745Pro)not specified [RCV004344634]uncertain significance8123808988123808988Humanname
401930648CV2828487single nucleotide variantNM_144963.4(FAM91A1):c.2364G>T (p.Glu788Asp)not provided [RCV003440622]likely benign8123812551123812551Humanname
405761829CV3252916single nucleotide variantNM_144963.4(FAM91A1):c.1327C>T (p.Leu443Phe)not specified [RCV004383632]uncertain significance8123789661123789661Humanname
405761843CV3252918single nucleotide variantNM_144963.4(FAM91A1):c.1579C>G (p.Pro527Ala)not specified [RCV004383634]uncertain significance8123799538123799538Humanname
405761847CV3252919single nucleotide variantNM_144963.4(FAM91A1):c.1891C>T (p.Arg631Cys)not specified [RCV004383635]uncertain significance8123806088123806088Humanname
405761856CV3252920single nucleotide variantNM_144963.4(FAM91A1):c.2321A>G (p.His774Arg)not specified [RCV004383636]uncertain significance8123810341123810341Humanname
405761861CV3252921single nucleotide variantNM_144963.4(FAM91A1):c.2473C>T (p.Arg825Trp)not specified [RCV004383637]uncertain significance8123812660123812660Humanname
407492129CV3431982single nucleotide variantNM_144963.4(FAM91A1):c.1877A>C (p.Gln626Pro)not specified [RCV004620680]uncertain significance8123805334123805334Humanname
407492134CV3431983single nucleotide variantNM_144963.4(FAM91A1):c.2111T>C (p.Ile704Thr)not specified [RCV004620681]uncertain significance8123808350123808350Humanname
597750911CV3675494single nucleotide variantNM_144963.4(FAM91A1):c.2067T>A (p.Asn689Lys)not specified [RCV004923628]uncertain significance8123808306123808306Humanname
597750933CV3675498single nucleotide variantNM_144963.4(FAM91A1):c.1136C>T (p.Ala379Val)not specified [RCV004923632]uncertain significance8123787318123787318Humanname
598238905CV3958616single nucleotide variantNM_144963.4(FAM91A1):c.1996G>T (p.Ala666Ser)not specified [RCV005343889]uncertain significance8123806193123806193Humanname
598238910CV3958617single nucleotide variantNM_144963.4(FAM91A1):c.2090T>C (p.Met697Thr)not specified [RCV005343890]uncertain significance8123808329123808329Humanname
598238916CV3958618single nucleotide variantNM_144963.4(FAM91A1):c.1689A>G (p.Ile563Met)not specified [RCV005343891]uncertain significance8123799648123799648Humanname
598238921CV3958619single nucleotide variantNM_144963.4(FAM91A1):c.2096T>C (p.Ile699Thr)not specified [RCV005343892]uncertain significance8123808335123808335Humanname
598238927CV3958620single nucleotide variantNM_144963.4(FAM91A1):c.2170G>A (p.Glu724Lys)not specified [RCV005343893]uncertain significance8123808925123808925Humanname
15134197CV711275single nucleotide variantNM_144963.4(FAM91A1):c.2110A>G (p.Ile704Val)not provided [RCV000965085]benign8123808349123808349Humanname