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54 records found for search term Asnsd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401917369CV2819435single nucleotide variantNM_019048.4(ASNSD1):c.-226C>Tnot provided [RCV003429466]likely benign2189661607189661607Humanname
597734225CV3597751single nucleotide variantNM_019048.4(ASNSD1):c.89G>A (p.Arg30Gln)not specified [RCV004863443]uncertain significance2189666221189666221Humanname
156063742CV2199964single nucleotide variantNM_019048.4(ASNSD1):c.113T>C (p.Leu38Ser)not specified [RCV004074135]uncertain significance2189666245189666245Humanname
329382111CV2424334single nucleotide variantNM_019048.4(ASNSD1):c.157G>A (p.Val53Ile)not specified [RCV004252240]uncertain significance2189666289189666289Humanname
407501254CV3480553single nucleotide variantNM_019048.4(ASNSD1):c.286T>C (p.Phe96Leu)not specified [RCV004669698]uncertain significance2189666418189666418Humanname
598205562CV3909698single nucleotide variantNM_019048.4(ASNSD1):c.243T>A (p.Ser81Arg)not specified [RCV005269717]uncertain significance2189666375189666375Humanname
8630101CV85248single nucleotide variantNM_019048.2(ASNSD1):c.1446C>T (p.Ser482=)Malignant melanoma [RCV000065330]not provided2189667578189667578Humanname
156164565CV2315101single nucleotide variantNM_019048.4(ASNSD1):c.462C>G (p.Phe154Leu)not specified [RCV004165287]uncertain significance2189666594189666594Humanname
329376963CV2455136single nucleotide variantNM_019048.4(ASNSD1):c.361T>C (p.Phe121Leu)not specified [RCV004272380]uncertain significance2189666493189666493Humanname
329398728CV2471318single nucleotide variantNM_019048.4(ASNSD1):c.529G>C (p.Gly177Arg)not specified [RCV004280331]uncertain significance2189666661189666661Humanname
329376621CV2472281single nucleotide variantNM_019048.4(ASNSD1):c.929A>G (p.Asn310Ser)not specified [RCV004285176]likely benign2189667061189667061Humanname
401776202CV2692633single nucleotide variantNM_019048.4(ASNSD1):c.488C>T (p.Thr163Ile)not specified [RCV004312363]uncertain significance2189666620189666620Humanname
405676826CV3283163single nucleotide variantNM_019048.4(ASNSD1):c.520C>G (p.Pro174Ala)not specified [RCV004420824]uncertain significance2189666652189666652Humanname
405676832CV3283164single nucleotide variantNM_019048.4(ASNSD1):c.670G>T (p.Ala224Ser)not specified [RCV004420825]uncertain significance2189666802189666802Humanname
405676837CV3283165single nucleotide variantNM_019048.4(ASNSD1):c.802G>A (p.Glu268Lys)not specified [RCV004420826]uncertain significance2189666934189666934Humanname
407519169CV3480516single nucleotide variantNM_019048.4(ASNSD1):c.585A>T (p.Gln195His)not specified [RCV004676373]uncertain significance2189666717189666717Humanname
407493456CV3480537single nucleotide variantNM_019048.4(ASNSD1):c.637A>G (p.Asn213Asp)not specified [RCV004667388]uncertain significance2189666769189666769Humanname
597734221CV3597750single nucleotide variantNM_019048.4(ASNSD1):c.859A>G (p.Ile287Val)not specified [RCV004863442]uncertain significance2189666991189666991Humanname
597734235CV3597754single nucleotide variantNM_019048.4(ASNSD1):c.419G>A (p.Arg140His)not specified [RCV004863445]uncertain significance2189666551189666551Humanname
597734247CV3597757single nucleotide variantNM_019048.4(ASNSD1):c.418C>T (p.Arg140Cys)not specified [RCV004863447]uncertain significance2189666550189666550Humanname
597734255CV3597762single nucleotide variantNM_019048.4(ASNSD1):c.878C>T (p.Ala293Val)not specified [RCV004863448]uncertain significance2189667010189667010Humanname
598205574CV3909700single nucleotide variantNM_019048.4(ASNSD1):c.592C>A (p.Pro198Thr)not specified [RCV005269719]uncertain significance2189666724189666724Humanname
156397516CV2197175single nucleotide variantNM_019048.4(ASNSD1):c.1178C>G (p.Ala393Gly)not specified [RCV004078966]uncertain significance2189667310189667310Humanname
156031811CV2218128single nucleotide variantNM_019048.4(ASNSD1):c.1348C>T (p.Arg450Trp)not specified [RCV004086556]likely benign2189667480189667480Humanname
156138750CV2250302single nucleotide variantNM_019048.4(ASNSD1):c.1520G>A (p.Arg507His)not specified [RCV004127200]uncertain significance2189667819189667819Humanname
156268845CV2293079single nucleotide variantNM_019048.4(ASNSD1):c.1688C>A (p.Ser563Tyr)not specified [RCV004148822]uncertain significance2189670482189670482Humanname
156290101CV2309787single nucleotide variantNM_019048.4(ASNSD1):c.1583G>A (p.Arg528Gln)not specified [RCV004160907]uncertain significance2189667882189667882Humanname
155974013CV2317799single nucleotide variantNM_019048.4(ASNSD1):c.1846A>G (p.Ile616Val)not specified [RCV004175047]uncertain significance2189670640189670640Humanname
155924259CV2347652single nucleotide variantNM_019048.4(ASNSD1):c.1378A>G (p.Ile460Val)not specified [RCV004200586]uncertain significance2189667510189667510Humanname
156390228CV2373201single nucleotide variantNM_019048.4(ASNSD1):c.1513C>T (p.Arg505Cys)not specified [RCV004217880]uncertain significance2189667812189667812Humanname
156077023CV2375077single nucleotide variantNM_019048.4(ASNSD1):c.1448A>G (p.Tyr483Cys)not specified [RCV004230125]uncertain significance2189667580189667580Humanname
156196378CV2400616single nucleotide variantNM_019048.4(ASNSD1):c.1727G>A (p.Arg576Gln)not specified [RCV004242302]uncertain significance2189670521189670521Humanname
329367098CV2430892single nucleotide variantNM_019048.4(ASNSD1):c.1049A>G (p.Asp350Gly)not specified [RCV004248089]uncertain significance2189667181189667181Humanname
329366111CV2438117single nucleotide variantNM_019048.4(ASNSD1):c.1414G>T (p.Gly472Cys)not specified [RCV004256898]uncertain significance2189667546189667546Humanname
329380623CV2444487single nucleotide variantNM_019048.4(ASNSD1):c.1694C>T (p.Pro565Leu)not specified [RCV004263217]uncertain significance2189670488189670488Humanname
401781709CV2682113single nucleotide variantNM_019048.4(ASNSD1):c.1707A>T (p.Lys569Asn)not specified [RCV004290169]uncertain significance2189670501189670501Humanname
401729446CV2683684single nucleotide variantNM_019048.4(ASNSD1):c.1075G>A (p.Glu359Lys)not specified [RCV004284433]likely benign2189667207189667207Humanname
401758616CV2700640single nucleotide variantNM_019048.4(ASNSD1):c.1625G>T (p.Gly542Val)not specified [RCV004313364]uncertain significance2189667924189667924Humanname
401720058CV2705634single nucleotide variantNM_019048.4(ASNSD1):c.1694C>G (p.Pro565Arg)not specified [RCV004318493]uncertain significance2189670488189670488Humanname
401776768CV2711344single nucleotide variantNM_019048.4(ASNSD1):c.1883A>T (p.Gln628Leu)not specified [RCV004313109]uncertain significance2189670677189670677Humanname
401887358CV2773397single nucleotide variantNM_019048.4(ASNSD1):c.1502C>T (p.Ala501Val)not specified [RCV004354041]uncertain significance2189667801189667801Humanname
405676788CV3283156single nucleotide variantNM_019048.4(ASNSD1):c.1045A>G (p.Ile349Val)not specified [RCV004420817]uncertain significance2189667177189667177Humanname
405676800CV3283158single nucleotide variantNM_019048.4(ASNSD1):c.1159A>G (p.Lys387Glu)not specified [RCV004420819]uncertain significance2189667291189667291Humanname
405676804CV3283159single nucleotide variantNM_019048.4(ASNSD1):c.1517A>G (p.His506Arg)not specified [RCV004420820]uncertain significance2189667816189667816Humanname
405677106CV3283160single nucleotide variantNM_019048.4(ASNSD1):c.1613A>T (p.Asp538Val)not specified [RCV004420821]uncertain significance2189667912189667912Humanname
405676815CV3283161single nucleotide variantNM_019048.4(ASNSD1):c.1822T>A (p.Ser608Thr)not specified [RCV004420822]uncertain significance2189670616189670616Humanname
407493428CV3480526single nucleotide variantNM_019048.4(ASNSD1):c.1022G>A (p.Arg341His)not specified [RCV004667381]uncertain significance2189667154189667154Humanname
407493492CV3480547single nucleotide variantNM_019048.4(ASNSD1):c.1828A>G (p.Ile610Val)not specified [RCV004667396]uncertain significance2189670622189670622Humanname
597734209CV3597748single nucleotide variantNM_019048.4(ASNSD1):c.1268G>A (p.Arg423Gln)not specified [RCV004863440]uncertain significance2189667400189667400Humanname
597734231CV3597752single nucleotide variantNM_019048.4(ASNSD1):c.1480A>G (p.Ile494Val)not specified [RCV004863444]uncertain significance2189667779189667779Humanname
597734241CV3597755single nucleotide variantNM_019048.4(ASNSD1):c.1888A>G (p.Met630Val)not specified [RCV004863446]uncertain significance2189670682189670682Humanname
598205516CV3909692single nucleotide variantNM_019048.4(ASNSD1):c.1271T>A (p.Ile424Asn)not specified [RCV005269711]uncertain significance2189667403189667403Humanname
598205524CV3909693single nucleotide variantNM_019048.4(ASNSD1):c.1370A>C (p.Asp457Ala)not specified [RCV005269712]uncertain significance2189667502189667502Humanname
598205597CV3909703single nucleotide variantNM_019048.4(ASNSD1):c.1230G>T (p.Arg410Ser)not specified [RCV005269722]uncertain significance2189667362189667362Humanname