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Variants search result for Homo sapiens
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34 records found for search term Anxa5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8567853CV38646variationANXA5, M2 HAPLOTYPEPregnancy loss, recurrent, susceptibility to, 3 [RCV000022537]risk factorHumanname
405292082CV3217062single nucleotide variantNM_001154.4(ANXA5):c.-1C>TANXA5-related disorder [RCV003964337]benign4121696590121696590Humanname , trait , alternate_id
597638231CV3555152single nucleotide variantNM_001154.4(ANXA5):c.5C>T (p.Ala2Val)not specified [RCV004831665]uncertain significance4121696585121696585Humanname
401744013CV2722349single nucleotide variantNM_001154.4(ANXA5):c.78G>T (p.Lys26Asn)not specified [RCV004322760]uncertain significance4121686304121686304Humanname
401896630CV2791820single nucleotide variantNM_001154.4(ANXA5):c.28A>G (p.Thr10Ala)not specified [RCV004359271]uncertain significance4121686354121686354Humanname
405696628CV3278833single nucleotide variantNM_001154.4(ANXA5):c.53G>A (p.Arg18Gln)not specified [RCV004424654]uncertain significance4121686329121686329Humanname
407497146CV3451392single nucleotide variantNM_001154.4(ANXA5):c.29C>T (p.Thr10Ile)not specified [RCV004643674]uncertain significance4121686353121686353Humanname
597637968CV3555162single nucleotide variantNM_001154.4(ANXA5):c.46G>C (p.Asp16His)not specified [RCV004831672]uncertain significance4121686336121686336Humanname
598263830CV3982908single nucleotide variantNM_001154.4(ANXA5):c.82A>T (p.Met28Leu)not specified [RCV005387583]uncertain significance4121686300121686300Humanname
15178442CV720736single nucleotide variantNM_001154.4(ANXA5):c.771T>C (p.Tyr257=)not provided [RCV000885063]likely benign4121669963121669963Humanname
15195347CV748704single nucleotide variantNM_001154.4(ANXA5):c.510T>C (p.Ala170=)not provided [RCV000911391]benign4121677915121677915Humanname
156076285CV2198158single nucleotide variantNM_001154.4(ANXA5):c.296C>T (p.Ala99Val)not specified [RCV004079747]uncertain significance4121683371121683371Humanname
156333755CV2220878single nucleotide variantNM_001154.4(ANXA5):c.260C>G (p.Pro87Arg)not specified [RCV004092305]uncertain significance4121683407121683407Humanname
156308717CV2249550single nucleotide variantNM_001154.4(ANXA5):c.119C>T (p.Thr40Ile)not specified [RCV004120578]uncertain significance4121684747121684747Humanname
155963809CV2330371single nucleotide variantNM_001154.4(ANXA5):c.265C>T (p.Arg89Trp)not specified [RCV004180946]uncertain significance4121683402121683402Humanname
405696608CV3278830single nucleotide variantNM_001154.4(ANXA5):c.160T>A (p.Ser54Thr)not specified [RCV004424651]uncertain significance4121684706121684706Humanname
15099421CV698355single nucleotide variantNM_001154.4(ANXA5):c.242T>C (p.Ile81Thr)not provided [RCV000958759]likely benign4121683425121683425Humanname
156246634CV2219120single nucleotide variantNM_001154.4(ANXA5):c.896T>C (p.Met299Thr)not specified [RCV004087278]uncertain significance4121669609121669609Humanname
156133528CV2284586single nucleotide variantNM_001154.4(ANXA5):c.382G>C (p.Val128Leu)not specified [RCV004140753]uncertain significance4121681683121681683Humanname
155972649CV2309430single nucleotide variantNM_001154.4(ANXA5):c.341T>G (p.Ile114Ser)not specified [RCV004165572]uncertain significance4121681724121681724Humanname
156387123CV2372644single nucleotide variantNM_001154.4(ANXA5):c.658C>G (p.Gln220Glu)not specified [RCV004221846]uncertain significance4121671610121671610Humanname
401775812CV2692501single nucleotide variantNM_001154.4(ANXA5):c.575A>G (p.Glu192Gly)not specified [RCV004312252]uncertain significance4121672583121672583Humanname
401747854CV2699935single nucleotide variantNM_001154.4(ANXA5):c.602G>T (p.Arg201Leu)not specified [RCV004310381]uncertain significance4121672556121672556Humanname
405285785CV3209707single nucleotide variantNM_001154.4(ANXA5):c.836T>C (p.Ile279Thr)ANXA5-related disorder [RCV003959274]likely benign4121669669121669669Humanname , trait , alternate_id
405696614CV3278831single nucleotide variantNM_001154.4(ANXA5):c.421G>A (p.Val141Met)not specified [RCV004424652]uncertain significance4121678468121678468Humanname
405696619CV3278832single nucleotide variantNM_001154.4(ANXA5):c.431A>G (p.Asp144Gly)not specified [RCV004424653]uncertain significance4121678458121678458Humanname
405696635CV3278834single nucleotide variantNM_001154.4(ANXA5):c.563G>C (p.Gly188Ala)not specified [RCV004424655]uncertain significance4121672595121672595Humanname
405696645CV3278835single nucleotide variantNM_001154.4(ANXA5):c.710T>A (p.Leu237His)not specified [RCV004424656]uncertain significance4121671558121671558Humanname
405696650CV3278836single nucleotide variantNM_001154.4(ANXA5):c.814G>A (p.Val272Ile)not specified [RCV004424657]uncertain significance4121669691121669691Humanname
405855392CV3394155single nucleotide variantNM_001154.4(ANXA5):c.652G>C (p.Gly218Arg)Pregnancy loss, recurrent, susceptibility to, 3 [RCV004547382]uncertain significance4121671616121671616Human1name
407497131CV3451383single nucleotide variantNM_001154.4(ANXA5):c.679C>T (p.Arg227Cys)not specified [RCV004643671]uncertain significance4121671589121671589Humanname
407508469CV3451401single nucleotide variantNM_001154.4(ANXA5):c.803C>G (p.Thr268Ser)not specified [RCV004647131]uncertain significance4121669702121669702Humanname
597637925CV3555148single nucleotide variantNM_001154.4(ANXA5):c.775A>G (p.Met259Val)not specified [RCV004831664]uncertain significance4121669959121669959Humanname
598229401CV3982909single nucleotide variantNM_001154.4(ANXA5):c.740T>C (p.Ile247Thr)not specified [RCV005381017]uncertain significance4121669994121669994Humanname