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54 records found for search term Asap1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15164448CV777750duplicationNM_018482.4(ASAP1):c.1169-8dupnot provided [RCV000948344]benign8130134351130134352Humanname
15164451CV700393single nucleotide variantNM_018482.4(ASAP1):c.789G>A (p.Gln263=)not provided [RCV000948345]benign8130169025130169025Humanname
401930730CV2828511single nucleotide variantNM_018482.4(ASAP1):c.2814C>T (p.Asp938=)not provided [RCV003440644]likely benign8130060957130060957Humanname
329385462CV2451463single nucleotide variantNM_018482.4(ASAP1):c.626A>G (p.Lys209Arg)not specified [RCV004272133]uncertain significance8130180785130180785Humanname
401876263CV2774429single nucleotide variantNM_018482.4(ASAP1):c.635G>A (p.Arg212His)not specified [RCV004347768]uncertain significance8130180776130180776Humanname
401867098CV2792604single nucleotide variantNM_018482.4(ASAP1):c.400A>T (p.Asn134Tyr)not specified [RCV004363628]uncertain significance8130214561130214561Humanname
401930731CV2828510single nucleotide variantNM_018482.4(ASAP1):c.3162G>A (p.Thr1054=)not provided [RCV003440643]likely benign8130060609130060609Humanname
407491936CV3476555single nucleotide variantNM_018482.4(ASAP1):c.722T>C (p.Ile241Thr)not specified [RCV004666983]uncertain significance8130179288130179288Humanname
597777137CV3583549single nucleotide variantNM_018482.4(ASAP1):c.518A>T (p.Tyr173Phe)not specified [RCV004852676]uncertain significance8130187248130187248Humanname
597789299CV3583625single nucleotide variantNM_018482.4(ASAP1):c.734A>G (p.His245Arg)not specified [RCV004855718]uncertain significance8130179276130179276Humanname
597777374CV3583638single nucleotide variantNM_018482.4(ASAP1):c.503A>G (p.Lys168Arg)not specified [RCV004852730]uncertain significance8130187263130187263Humanname
598166446CV3909157single nucleotide variantNM_018482.4(ASAP1):c.938G>A (p.Ser313Asn)not specified [RCV005262063]uncertain significance8130159936130159936Humanname
598166522CV3909171single nucleotide variantNM_018482.4(ASAP1):c.337G>A (p.Asp113Asn)not specified [RCV005262077]uncertain significance8130214624130214624Humanname
156185409CV2222611single nucleotide variantNM_018482.4(ASAP1):c.1055G>A (p.Gly352Glu)not specified [RCV004099438]uncertain significance8130152761130152761Humanname
156199121CV2331233single nucleotide variantNM_018482.4(ASAP1):c.1825G>A (p.Val609Ile)not specified [RCV004181836]uncertain significance8130118216130118216Humanname
156080827CV2368738single nucleotide variantNM_018482.4(ASAP1):c.2362A>G (p.Thr788Ala)not specified [RCV004214621]likely benign8130112133130112133Humanname
156150575CV2394662single nucleotide variantNM_018482.4(ASAP1):c.1858G>A (p.Val620Ile)not specified [RCV004240999]uncertain significance8130118183130118183Humanname
329363577CV2442315single nucleotide variantNM_018482.4(ASAP1):c.2619T>G (p.Phe873Leu)not specified [RCV004264789]uncertain significance8130079925130079925Humanname
329362389CV2444665single nucleotide variantNM_018482.4(ASAP1):c.1748A>G (p.Tyr583Cys)not specified [RCV004258927]uncertain significance8130118535130118535Humanname
401729032CV2673129single nucleotide variantNM_018482.4(ASAP1):c.2249A>G (p.Lys750Arg)not specified [RCV004284112]uncertain significance8130112246130112246Humanname
401776199CV2692632single nucleotide variantNM_018482.4(ASAP1):c.2452G>A (p.Gly818Ser)not specified [RCV004312362]uncertain significance8130092093130092093Humanname
401760717CV2706063single nucleotide variantNM_018482.4(ASAP1):c.1741C>A (p.Gln581Lys)not specified [RCV004314758]uncertain significance8130118542130118542Humanname
401767427CV2727160single nucleotide variantNM_018482.4(ASAP1):c.1298G>A (p.Ser433Asn)not specified [RCV004325514]uncertain significance8130128010130128010Humanname
401876353CV2770535single nucleotide variantNM_018482.4(ASAP1):c.2237C>T (p.Ser746Phe)not specified [RCV004347815]uncertain significance8130112258130112258Humanname
401871765CV2783594single nucleotide variantNM_018482.4(ASAP1):c.2431C>A (p.Leu811Ile)not specified [RCV004365916]uncertain significance8130092114130092114Humanname
401898573CV2784686single nucleotide variantNM_018482.4(ASAP1):c.1649A>G (p.His550Arg)not specified [RCV004352501]uncertain significance8130118634130118634Humanname
405675356CV3286635single nucleotide variantNM_018482.4(ASAP1):c.1295A>G (p.Asn432Ser)not specified [RCV004420443]uncertain significance8130128013130128013Humanname
405675352CV3286636single nucleotide variantNM_018482.4(ASAP1):c.2048C>G (p.Thr683Ser)not specified [RCV004420444]uncertain significance8130116694130116694Humanname
405675347CV3286637single nucleotide variantNM_018482.4(ASAP1):c.2363C>T (p.Thr788Met)not specified [RCV004420445]uncertain significance8130112132130112132Humanname
405675342CV3286638single nucleotide variantNM_018482.4(ASAP1):c.2429C>T (p.Pro810Leu)not specified [RCV004420446]uncertain significance8130092116130092116Humanname
405675190CV3286639single nucleotide variantNM_018482.4(ASAP1):c.2867C>T (p.Pro956Leu)not specified [RCV004420447]uncertain significance8130060904130060904Humanname
407476610CV3476544single nucleotide variantNM_018482.4(ASAP1):c.2497G>A (p.Gly833Arg)not specified [RCV004663518]uncertain significance8130092048130092048Humanname
597777110CV3583539single nucleotide variantNM_018482.4(ASAP1):c.2968C>G (p.Pro990Ala)not specified [RCV004852670]uncertain significance8130060803130060803Humanname
597777172CV3583560single nucleotide variantNM_018482.4(ASAP1):c.1289G>A (p.Gly430Glu)not specified [RCV004852684]uncertain significance8130128019130128019Humanname
597777202CV3583571single nucleotide variantNM_018482.4(ASAP1):c.1715A>G (p.Lys572Arg)not specified [RCV004852691]uncertain significance8130118568130118568Humanname
597777228CV3583582single nucleotide variantNM_018482.4(ASAP1):c.2944C>T (p.Pro982Ser)not specified [RCV004852697]uncertain significance8130060827130060827Humanname
597789254CV3583593single nucleotide variantNM_018482.4(ASAP1):c.1894A>G (p.Lys632Glu)not specified [RCV004855706]uncertain significance8130116982130116982Humanname
597777274CV3583603single nucleotide variantNM_018482.4(ASAP1):c.1201G>A (p.Glu401Lys)not specified [RCV004852707]uncertain significance8130134312130134312Humanname
597789284CV3583614single nucleotide variantNM_018482.4(ASAP1):c.1172A>G (p.Asn391Ser)not specified [RCV004855714]uncertain significance8130134341130134341Humanname
597777357CV3583631single nucleotide variantNM_018482.4(ASAP1):c.1391G>T (p.Trp464Leu)not specified [RCV004852726]uncertain significance8130126080130126080Humanname
597777400CV3583649single nucleotide variantNM_018482.4(ASAP1):c.1879T>C (p.Cys627Arg)not specified [RCV004852736]uncertain significance8130118162130118162Humanname
598166458CV3909159single nucleotide variantNM_018482.4(ASAP1):c.2326G>A (p.Val776Ile)not specified [RCV005262065]uncertain significance8130112169130112169Humanname
598166489CV3909165single nucleotide variantNM_018482.4(ASAP1):c.1883G>A (p.Gly628Glu)not specified [RCV005262071]uncertain significance8130116993130116993Humanname
598166501CV3909167single nucleotide variantNM_018482.4(ASAP1):c.2407A>C (p.Thr803Pro)not specified [RCV005262073]uncertain significance8130092138130092138Humanname
598166557CV3909178single nucleotide variantNM_018482.4(ASAP1):c.2233A>G (p.Ile745Val)not specified [RCV005262084]uncertain significance8130112262130112262Humanname
598166573CV3909181single nucleotide variantNM_018482.4(ASAP1):c.2354C>T (p.Ser785Leu)not specified [RCV005262087]uncertain significance8130112141130112141Humanname
155953207CV2306379single nucleotide variantNM_018482.4(ASAP1):c.3104C>G (p.Ala1035Gly)not specified [RCV004163076]uncertain significance8130060667130060667Humanname
156143440CV2358578single nucleotide variantNM_018482.4(ASAP1):c.3136G>A (p.Asp1046Asn)not specified [RCV004207459]uncertain significance8130060635130060635Humanname
401762419CV2723434single nucleotide variantNM_018482.4(ASAP1):c.3191C>T (p.Thr1064Met)not specified [RCV004323509]uncertain significance8130060580130060580Humanname
401887242CV2773259single nucleotide variantNM_018482.4(ASAP1):c.3325A>G (p.Ile1109Val)not specified [RCV004353931]uncertain significance8130054796130054796Humanname
405675103CV3286640single nucleotide variantNM_018482.4(ASAP1):c.3068C>T (p.Pro1023Leu)not specified [RCV004420448]uncertain significance8130060703130060703Humanname
405675023CV3286641single nucleotide variantNM_018482.4(ASAP1):c.3371T>C (p.Val1124Ala)not specified [RCV004420449]uncertain significance8130054750130054750Humanname
598166472CV3909162single nucleotide variantNM_018482.4(ASAP1):c.3064C>T (p.His1022Tyr)not specified [RCV005262068]uncertain significance8130060707130060707Humanname
598166532CV3909173single nucleotide variantNM_018482.4(ASAP1):c.3286G>A (p.Val1096Ile)not specified [RCV005262079]uncertain significance8130057983130057983Humanname