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Variants search result for All species
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54 records found for search term Fam114a2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580450CV114880single nucleotide variantNM_018691.2(FAM114A2):c.993+2455G>CLung cancer [RCV000095403]uncertain significance5154008786154008786Humanname
597719210CV3671883single nucleotide variantNM_018691.4(FAM114A2):c.17A>T (p.Asp6Val)not specified [RCV004918614]uncertain significance5154034937154034937Humanname
155999174CV2396378single nucleotide variantNM_018691.4(FAM114A2):c.84G>T (p.Lys28Asn)not specified [RCV004242100]uncertain significance5154034870154034870Humanname
401720007CV2705614single nucleotide variantNM_018691.4(FAM114A2):c.73G>A (p.Glu25Lys)not specified [RCV004318476]uncertain significance5154034881154034881Humanname
598223900CV3965748single nucleotide variantNM_018691.4(FAM114A2):c.76C>A (p.Pro26Thr)not specified [RCV005341225]uncertain significance5154034878154034878Humanname
155970769CV2262275single nucleotide variantNM_018691.4(FAM114A2):c.181C>G (p.Leu61Val)not specified [RCV004128478]uncertain significance5154034773154034773Humanname
155993667CV2379444single nucleotide variantNM_018691.4(FAM114A2):c.149G>A (p.Arg50Gln)not specified [RCV004223893]uncertain significance5154034805154034805Humanname
156391759CV2382549single nucleotide variantNM_018691.4(FAM114A2):c.290C>T (p.Ser97Leu)not specified [RCV004232879]uncertain significance5154034298154034298Humanname
401890501CV2768021single nucleotide variantNM_018691.4(FAM114A2):c.281C>T (p.Ser94Phe)not specified [RCV004348265]uncertain significance5154034307154034307Humanname
405725512CV3249728single nucleotide variantNM_018691.4(FAM114A2):c.193A>G (p.Lys65Glu)not specified [RCV004378548]likely benign5154034761154034761Humanname
405725521CV3249729single nucleotide variantNM_018691.4(FAM114A2):c.213T>G (p.Asp71Glu)not specified [RCV004378549]likely benign5154034375154034375Humanname
598223908CV3965750single nucleotide variantNM_018691.4(FAM114A2):c.131A>G (p.Glu44Gly)not specified [RCV005341226]uncertain significance5154034823154034823Humanname
150456110CV1278454single nucleotide variantNM_018691.4(FAM114A2):c.364G>A (p.Gly122Ser)not provided [RCV001709069]benign5154033830154033830Human4name
156380936CV2218413single nucleotide variantNM_018691.4(FAM114A2):c.970T>G (p.Ser324Ala)not specified [RCV004090704]uncertain significance5154011264154011264Humanname
156380484CV2218771single nucleotide variantNM_018691.4(FAM114A2):c.515G>A (p.Gly172Glu)not specified [RCV004085023]uncertain significance5154028264154028264Humanname
155979548CV2243816single nucleotide variantNM_018691.4(FAM114A2):c.302C>T (p.Ala101Val)not specified [RCV004114776]uncertain significance5154034286154034286Humanname
156311865CV2256779single nucleotide variantNM_018691.4(FAM114A2):c.566C>T (p.Ala189Val)not specified [RCV004121003]uncertain significance5154028213154028213Humanname
156003343CV2258058single nucleotide variantNM_018691.4(FAM114A2):c.989C>T (p.Ala330Val)not specified [RCV004129853]uncertain significance5154011245154011245Humanname
156176092CV2299753single nucleotide variantNM_018691.4(FAM114A2):c.508A>G (p.Ile170Val)not specified [RCV004148913]uncertain significance5154028271154028271Humanname
155925516CV2365594single nucleotide variantNM_018691.4(FAM114A2):c.685G>A (p.Val229Met)not specified [RCV004212114]likely benign5154027280154027280Humanname
155996772CV2398605single nucleotide variantNM_018691.4(FAM114A2):c.940A>G (p.Thr314Ala)not specified [RCV004237915]uncertain significance5154011294154011294Humanname
329366506CV2445788single nucleotide variantNM_018691.4(FAM114A2):c.832A>T (p.Thr278Ser)not specified [RCV004259846]uncertain significance5154026480154026480Humanname
401739405CV2722122single nucleotide variantNM_018691.4(FAM114A2):c.958C>G (p.Leu320Val)not specified [RCV004328381]uncertain significance5154011276154011276Humanname
401889082CV2761748single nucleotide variantNM_018691.4(FAM114A2):c.937A>G (p.Ile313Val)not specified [RCV004337356]uncertain significance5154011297154011297Humanname
405725527CV3249730single nucleotide variantNM_018691.4(FAM114A2):c.304A>G (p.Thr102Ala)not specified [RCV004378550]uncertain significance5154034284154034284Humanname
405725539CV3249731single nucleotide variantNM_018691.4(FAM114A2):c.416C>T (p.Ala139Val)not specified [RCV004378551]uncertain significance5154029568154029568Humanname
405725547CV3249732single nucleotide variantNM_018691.4(FAM114A2):c.553A>G (p.Met185Val)not specified [RCV004378552]uncertain significance5154028226154028226Humanname
405725557CV3249733single nucleotide variantNM_018691.4(FAM114A2):c.619A>G (p.Thr207Ala)not specified [RCV004378553]uncertain significance5154028160154028160Humanname
405725567CV3249734single nucleotide variantNM_018691.4(FAM114A2):c.646A>G (p.Lys216Glu)not specified [RCV004378554]uncertain significance5154027319154027319Humanname
405725578CV3249735single nucleotide variantNM_018691.4(FAM114A2):c.952T>C (p.Ser318Pro)not specified [RCV004378555]uncertain significance5154011282154011282Humanname
597719129CV3671873single nucleotide variantNM_018691.4(FAM114A2):c.616G>A (p.Ala206Thr)not specified [RCV004918604]uncertain significance5154028163154028163Humanname
597719138CV3671874single nucleotide variantNM_018691.4(FAM114A2):c.445G>A (p.Ala149Thr)not specified [RCV004918605]uncertain significance5154029539154029539Humanname
597719146CV3671875single nucleotide variantNM_018691.4(FAM114A2):c.674A>G (p.Asn225Ser)not specified [RCV004918606]uncertain significance5154027291154027291Humanname
597719181CV3671879single nucleotide variantNM_018691.4(FAM114A2):c.836T>C (p.Leu279Pro)not specified [RCV004918610]uncertain significance5154026476154026476Humanname
597719188CV3671880single nucleotide variantNM_018691.4(FAM114A2):c.311G>T (p.Gly104Val)not specified [RCV004918611]uncertain significance5154033883154033883Humanname
597719195CV3671881single nucleotide variantNM_018691.4(FAM114A2):c.593C>G (p.Thr198Ser)not specified [RCV004918612]uncertain significance5154028186154028186Humanname
597719204CV3671882single nucleotide variantNM_018691.4(FAM114A2):c.727G>A (p.Glu243Lys)not specified [RCV004918613]uncertain significance5154027238154027238Humanname
598223887CV3965746single nucleotide variantNM_018691.4(FAM114A2):c.920A>C (p.Glu307Ala)not specified [RCV005341223]uncertain significance5154011314154011314Humanname
598223895CV3965747single nucleotide variantNM_018691.4(FAM114A2):c.644C>T (p.Ala215Val)not specified [RCV005341224]uncertain significance5154027321154027321Humanname
598194893CV3965749single nucleotide variantNM_018691.4(FAM114A2):c.704C>T (p.Thr235Ile)not specified [RCV005335482]uncertain significance5154027261154027261Humanname
598223929CV3965753single nucleotide variantNM_018691.4(FAM114A2):c.754G>T (p.Ala252Ser)not specified [RCV005341229]uncertain significance5154027211154027211Humanname
8631498CV86702single nucleotide variantNM_018691.2(FAM114A2):c.968C>T (p.Ser323Phe)Malignant melanoma [RCV000066793]not provided5154011266154011266Humanname
156243779CV2283301single nucleotide variantNM_018691.4(FAM114A2):c.1392C>G (p.Asn464Lys)not specified [RCV004145963]uncertain significance5153993102153993102Humanname
156115673CV2349319single nucleotide variantNM_018691.4(FAM114A2):c.1127C>T (p.Ala376Val)not specified [RCV004199263]uncertain significance5154002380154002380Humanname
329377292CV2435872single nucleotide variantNM_018691.4(FAM114A2):c.1508T>C (p.Leu503Ser)not specified [RCV004255106]likely benign5153992986153992986Humanname
401746666CV2678892single nucleotide variantNM_018691.4(FAM114A2):c.1138C>T (p.Arg380Trp)not specified [RCV004292865]uncertain significance5154002369154002369Humanname
405725485CV3249725single nucleotide variantNM_018691.4(FAM114A2):c.1249C>T (p.Leu417Phe)not specified [RCV004378545]uncertain significance5154002258154002258Humanname
405725494CV3249726single nucleotide variantNM_018691.4(FAM114A2):c.1346A>G (p.Asp449Gly)not specified [RCV004378546]uncertain significance5153994956153994956Humanname
405725504CV3249727single nucleotide variantNM_018691.4(FAM114A2):c.1493G>T (p.Gly498Val)not specified [RCV004378547]likely benign5153993001153993001Humanname
407507805CV3435404single nucleotide variantNM_018691.4(FAM114A2):c.1244A>G (p.Gln415Arg)not specified [RCV004625209]likely benign5154002263154002263Humanname
407507810CV3435406single nucleotide variantNM_018691.4(FAM114A2):c.1489C>G (p.Gln497Glu)not specified [RCV004625211]uncertain significance5153993005153993005Humanname
597719154CV3671876single nucleotide variantNM_018691.4(FAM114A2):c.1280A>C (p.Glu427Ala)not specified [RCV004918607]uncertain significance5153997852153997852Humanname
597719171CV3671878single nucleotide variantNM_018691.4(FAM114A2):c.1237A>G (p.Arg413Gly)not specified [RCV004918609]uncertain significance5154002270154002270Humanname
598223922CV3965752single nucleotide variantNM_018691.4(FAM114A2):c.1286C>T (p.Ser429Phe)not specified [RCV005341228]uncertain significance5153997846153997846Humanname