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Variants search result for Homo sapiens
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46 records found for search term Hsf1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15184793CV711402single nucleotide variantNM_005526.4(HSF1):c.72C>A (p.Thr24=)not provided [RCV000975199]benign8144291829144291829Humanname
156368854CV2267099single nucleotide variantNM_005526.4(HSF1):c.94G>A (p.Asp32Asn)not specified [RCV004131720]uncertain significance8144291851144291851Humanname
401909310CV2828672single nucleotide variantNM_005526.4(HSF1):c.960C>T (p.Ser320=)not provided [RCV003423994]likely benign8144312062144312062Humanname
597774172CV3689721single nucleotide variantNM_005526.4(HSF1):c.39C>G (p.Ser13Arg)not specified [RCV004929045]uncertain significance8144291796144291796Humanname
15143980CV736533single nucleotide variantNM_005526.4(HSF1):c.429C>T (p.Asp143=)not provided [RCV000899927]benign8144309837144309837Humanname
15114297CV766633single nucleotide variantNM_005526.4(HSF1):c.711G>A (p.Ser237=)not provided [RCV000939290]likely benign8144311589144311589Humanname
405803632CV3274241single nucleotide variantNM_005526.4(HSF1):c.104T>C (p.Ile35Thr)not specified [RCV004404548]uncertain significance8144291861144291861Humanname
597774176CV3689722single nucleotide variantNM_005526.4(HSF1):c.185A>G (p.Lys62Arg)not specified [RCV004929046]uncertain significance8144308973144308973Humanname
598255817CV3968184single nucleotide variantNM_005526.4(HSF1):c.129C>A (p.Ser43Arg)not specified [RCV005346639]uncertain significance8144308917144308917Humanname
598255833CV3968187single nucleotide variantNM_005526.4(HSF1):c.200C>T (p.Ala67Val)not specified [RCV005346642]uncertain significance8144308988144308988Humanname
156037843CV2218690single nucleotide variantNM_005526.4(HSF1):c.936G>T (p.Glu312Asp)not specified [RCV004090939]uncertain significance8144312038144312038Humanname
156078188CV2248468single nucleotide variantNM_005526.4(HSF1):c.517G>A (p.Ala173Thr)not specified [RCV004119600]uncertain significance8144311202144311202Humanname
155925976CV2258663single nucleotide variantNM_005526.4(HSF1):c.478G>A (p.Ala160Thr)not specified [RCV004117911]uncertain significance8144309886144309886Humanname
156366860CV2269779single nucleotide variantNM_005526.4(HSF1):c.926G>A (p.Arg309Gln)not specified [RCV004127025]uncertain significance8144312028144312028Humanname
329356205CV2442514single nucleotide variantNM_005526.4(HSF1):c.556G>A (p.Val186Ile)not specified [RCV004266748]uncertain significance8144311241144311241Humanname
329375418CV2444821single nucleotide variantNM_005526.4(HSF1):c.317G>A (p.Arg106His)not specified [RCV004259062]uncertain significance8144309545144309545Humanname
329369311CV2450600single nucleotide variantNM_005526.4(HSF1):c.745A>G (p.Ser249Gly)not specified [RCV004265495]likely benign8144311721144311721Humanname
401781956CV2722356single nucleotide variantNM_005526.4(HSF1):c.677G>T (p.Ser226Ile)not specified [RCV004322766]uncertain significance8144311555144311555Humanname
401892638CV2782287single nucleotide variantNM_005526.4(HSF1):c.356T>G (p.Val119Gly)not specified [RCV004359251]uncertain significance8144309584144309584Humanname
405803640CV3274245single nucleotide variantNM_005526.4(HSF1):c.461T>C (p.Met154Thr)not specified [RCV004404552]uncertain significance8144309869144309869Humanname
405803641CV3274246single nucleotide variantNM_005526.4(HSF1):c.481A>G (p.Met161Val)not specified [RCV004404553]uncertain significance8144309889144309889Humanname
405803643CV3274247single nucleotide variantNM_005526.4(HSF1):c.751A>G (p.Ser251Gly)not specified [RCV004404554]uncertain significance8144311727144311727Humanname
405803645CV3274248single nucleotide variantNM_005526.4(HSF1):c.911C>T (p.Pro304Leu)not specified [RCV004404555]uncertain significance8144312013144312013Humanname
405803647CV3274249single nucleotide variantNM_005526.4(HSF1):c.979C>T (p.Pro327Ser)not specified [RCV004404556]uncertain significance8144312081144312081Humanname
407464869CV3444065single nucleotide variantNM_005526.4(HSF1):c.946G>A (p.Gly316Arg)not specified [RCV004635189]uncertain significance8144312048144312048Humanname
597774163CV3689719single nucleotide variantNM_005526.4(HSF1):c.953C>T (p.Pro318Leu)not specified [RCV004929043]uncertain significance8144312055144312055Humanname
598255828CV3968186single nucleotide variantNM_005526.4(HSF1):c.886C>T (p.Arg296Cys)not specified [RCV005346641]uncertain significance8144311988144311988Humanname
598255836CV3968188single nucleotide variantNM_005526.4(HSF1):c.905C>T (p.Pro302Leu)not specified [RCV005346643]uncertain significance8144312007144312007Humanname
156130529CV2235167single nucleotide variantNM_005526.4(HSF1):c.1488G>C (p.Glu496Asp)not specified [RCV004107226]uncertain significance8144314228144314228Humanname
155917830CV2236667single nucleotide variantNM_005526.4(HSF1):c.1297G>A (p.Asp433Asn)not specified [RCV004110631]uncertain significance8144313894144313894Humanname
155981837CV2244123single nucleotide variantNM_005526.4(HSF1):c.1436G>C (p.Gly479Ala)not specified [RCV004108584]uncertain significance8144314176144314176Humanname
156205686CV2297902single nucleotide variantNM_005526.4(HSF1):c.1235G>A (p.Ser412Asn)not specified [RCV004157835]uncertain significance8144313603144313603Humanname
156402770CV2371582single nucleotide variantNM_005526.4(HSF1):c.1331C>T (p.Ser444Phe)not specified [RCV004216829]uncertain significance8144314001144314001Humanname
329374427CV2434812single nucleotide variantNM_005526.4(HSF1):c.1027G>A (p.Ala343Thr)not specified [RCV004248501]uncertain significance8144312129144312129Humanname
401761034CV2706192single nucleotide variantNM_005526.4(HSF1):c.1432C>G (p.Pro478Ala)not specified [RCV004314870]uncertain significance8144314172144314172Humanname
401882271CV2793429single nucleotide variantNM_005526.4(HSF1):c.1365G>T (p.Glu455Asp)not specified [RCV004362521]uncertain significance8144314035144314035Humanname
405803634CV3274242single nucleotide variantNM_005526.4(HSF1):c.1209C>A (p.Ser403Arg)not specified [RCV004404549]uncertain significance8144313577144313577Humanname
405803636CV3274243single nucleotide variantNM_005526.4(HSF1):c.1450G>A (p.Gly484Arg)not specified [RCV004404550]uncertain significance8144314190144314190Humanname
405803638CV3274244single nucleotide variantNM_005526.4(HSF1):c.1522G>A (p.Glu508Lys)not specified [RCV004404551]uncertain significance8144314262144314262Humanname
597774167CV3689720single nucleotide variantNM_005526.4(HSF1):c.1019C>T (p.Pro340Leu)not specified [RCV004929044]uncertain significance8144312121144312121Humanname
597774181CV3689723single nucleotide variantNM_005526.4(HSF1):c.1373G>A (p.Ser458Asn)not specified [RCV004929047]uncertain significance8144314043144314043Humanname
597774186CV3689724single nucleotide variantNM_005526.4(HSF1):c.1463T>C (p.Leu488Pro)not specified [RCV004929048]uncertain significance8144314203144314203Humanname
597774189CV3689725single nucleotide variantNM_005526.4(HSF1):c.1444G>C (p.Asp482His)not specified [RCV004929049]uncertain significance8144314184144314184Humanname
597774193CV3689726single nucleotide variantNM_005526.4(HSF1):c.1109C>G (p.Pro370Arg)not specified [RCV004929050]uncertain significance8144312211144312211Humanname
597774198CV3689727single nucleotide variantNM_005526.4(HSF1):c.1267A>T (p.Thr423Ser)not specified [RCV004929051]uncertain significance8144313864144313864Humanname
598255823CV3968185single nucleotide variantNM_005526.4(HSF1):c.1064C>T (p.Thr355Met)not specified [RCV005346640]uncertain significance8144312166144312166Humanname