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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


38 records found for search term Serbp1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155990960CV2255595single nucleotide variantNM_001018069.2(SERBP1):c.696-8A>Gnot specified [RCV004120012]uncertain significance16742428567424285Humanname
597737647CV3598415single nucleotide variantNM_001018069.2(SERBP1):c.696-10A>Gnot specified [RCV004864082]uncertain significance16742428767424287Humanname
407488712CV3473592single nucleotide variantNM_001018069.2(SERBP1):c.4C>T (p.Pro2Ser)not specified [RCV004665918]uncertain significance16743029767430297Humanname
155978614CV2318102single nucleotide variantNM_001018069.2(SERBP1):c.52G>C (p.Asp18His)not specified [RCV004177519]uncertain significance16743024967430249Humanname
8625043CV80162single nucleotide variantNM_001018067.1(SERBP1):c.447C>T (p.Gly149=)Malignant melanoma [RCV000060238]not provided16742615267426152Humanname
156014075CV2300507single nucleotide variantNM_001018069.2(SERBP1):c.203A>G (p.Lys68Arg)not specified [RCV004153691]uncertain significance16743009867430098Humanname
405746347CV3310818single nucleotide variantNM_001018069.2(SERBP1):c.108C>A (p.Asn36Lys)not specified [RCV004453118]uncertain significance16743019367430193Humanname
405746365CV3310820single nucleotide variantNM_001018069.2(SERBP1):c.185A>C (p.Asn62Thr)not specified [RCV004453120]uncertain significance16743011667430116Humanname
405746371CV3310821single nucleotide variantNM_001018069.2(SERBP1):c.284C>T (p.Thr95Met)not specified [RCV004453121]uncertain significance16743001767430017Humanname
407488718CV3473596single nucleotide variantNM_001018069.2(SERBP1):c.247C>A (p.Pro83Thr)not specified [RCV004665919]uncertain significance16743005467430054Humanname
598225237CV3900352single nucleotide variantNM_001018069.2(SERBP1):c.247C>T (p.Pro83Ser)not specified [RCV005273319]uncertain significance16743005467430054Humanname
598225250CV3900354single nucleotide variantNM_001018069.2(SERBP1):c.290C>T (p.Pro97Leu)not specified [RCV005273321]uncertain significance16743001167430011Humanname
598225268CV3900357single nucleotide variantNM_001018069.2(SERBP1):c.274A>C (p.Lys92Gln)not specified [RCV005273324]uncertain significance16743002767430027Humanname
156387375CV2221489single nucleotide variantNM_001018069.2(SERBP1):c.745C>G (p.His249Asp)not specified [RCV004096767]uncertain significance16742422867424228Humanname
156356673CV2257485single nucleotide variantNM_001018069.2(SERBP1):c.953C>T (p.Ala318Val)not specified [RCV004125554]uncertain significance16741533867415338Humanname
156360141CV2268988single nucleotide variantNM_001018069.2(SERBP1):c.789A>C (p.Glu263Asp)not specified [RCV004128386]uncertain significance16742017167420171Humanname
156234537CV2271183single nucleotide variantNM_001018069.2(SERBP1):c.392G>A (p.Arg131Gln)not specified [RCV004134546]uncertain significance16742620767426207Humanname
155998913CV2287208single nucleotide variantNM_001018069.2(SERBP1):c.764C>A (p.Thr255Asn)not specified [RCV004146858]uncertain significance16742420967424209Humanname
156149358CV2321955single nucleotide variantNM_001018069.2(SERBP1):c.679G>A (p.Val227Ile)not specified [RCV004173411]uncertain significance16742490467424904Humanname
155958539CV2395203single nucleotide variantNM_001018069.2(SERBP1):c.775G>A (p.Glu259Lys)not specified [RCV004236871]uncertain significance16742018567420185Humanname
329374895CV2431085single nucleotide variantNM_001018069.2(SERBP1):c.731C>A (p.Pro244His)not specified [RCV004250449]uncertain significance16742424267424242Humanname
329353293CV2469109single nucleotide variantNM_001018069.2(SERBP1):c.841A>C (p.Ile281Leu)not specified [RCV004274341]uncertain significance16742011967420119Humanname
401758680CV2700693single nucleotide variantNM_001018069.2(SERBP1):c.542G>T (p.Arg181Leu)not specified [RCV004313406]uncertain significance16742514667425146Humanname
401857150CV2759986single nucleotide variantNM_001018069.2(SERBP1):c.467C>T (p.Pro156Leu)not specified [RCV004345404]uncertain significance16742522167425221Humanname
405746379CV3310822single nucleotide variantNM_001018069.2(SERBP1):c.569A>G (p.Lys190Arg)not specified [RCV004453122]uncertain significance16742511967425119Humanname
405746386CV3310823single nucleotide variantNM_001018069.2(SERBP1):c.710C>T (p.Ser237Leu)not specified [RCV004453123]uncertain significance16742426367424263Humanname
407492421CV3473593single nucleotide variantNM_001018069.2(SERBP1):c.793G>A (p.Val265Ile)not specified [RCV004667120]uncertain significance16742016767420167Humanname
597737637CV3598413single nucleotide variantNM_001018069.2(SERBP1):c.383C>T (p.Pro128Leu)not specified [RCV004864080]uncertain significance16742621667426216Humanname
597737642CV3598414single nucleotide variantNM_001018069.2(SERBP1):c.511G>A (p.Gly171Ser)not specified [RCV004864081]uncertain significance16742517767425177Humanname
598225244CV3900353single nucleotide variantNM_001018069.2(SERBP1):c.354G>C (p.Gln118His)not specified [RCV005273320]uncertain significance16742624567426245Humanname
598225257CV3900355single nucleotide variantNM_001018069.2(SERBP1):c.723G>C (p.Glu241Asp)not specified [RCV005273322]uncertain significance16742425067424250Humanname
598225263CV3900356single nucleotide variantNM_001018069.2(SERBP1):c.326T>C (p.Val109Ala)not specified [RCV005273323]uncertain significance16742627367426273Humanname
598225273CV3900358single nucleotide variantNM_001018069.2(SERBP1):c.394C>A (p.Pro132Thr)not specified [RCV005273325]uncertain significance16742620567426205Humanname
155903297CV2274854single nucleotide variantNM_001018069.2(SERBP1):c.1028A>G (p.Asn343Ser)not specified [RCV004133052]uncertain significance16741526367415263Humanname
405746357CV3310819single nucleotide variantNM_001018069.2(SERBP1):c.1121A>G (p.Asp374Gly)not specified [RCV004453119]uncertain significance16741517067415170Humanname
407492424CV3473594single nucleotide variantNM_001018069.2(SERBP1):c.1045C>T (p.Arg349Cys)not specified [RCV004667121]uncertain significance16741524667415246Humanname
597737627CV3598410single nucleotide variantNM_001018069.2(SERBP1):c.1120G>A (p.Asp374Asn)not specified [RCV004864078]uncertain significance16741517167415171Humanname
597737632CV3598411single nucleotide variantNM_001018069.2(SERBP1):c.1109G>T (p.Gly370Val)not specified [RCV004864079]uncertain significance16741518267415182Humanname