Fhdc1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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140 records found for search term Fhdc1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156070543	CV2204022	single nucleotide variant	NM_001371116.1(FHDC1):c.286C>T (p.Arg96Trp)	not specified [RCV004070060]	uncertain significance	4	152943343	152943343	Human		name
156000152	CV2287349	single nucleotide variant	NM_001371116.1(FHDC1):c.250C>T (p.His84Tyr)	not specified [RCV004146968]	uncertain significance	4	152943307	152943307	Human		name
401774180	CV2691545	single nucleotide variant	NM_001371116.1(FHDC1):c.125C>T (p.Pro42Leu)	not specified [RCV004305379]	uncertain significance	4	152943182	152943182	Human		name
401893316	CV2765102	single nucleotide variant	NM_001371116.1(FHDC1):c.202G>A (p.Gly68Arg)	not specified [RCV004337598]	uncertain significance	4	152943259	152943259	Human		name
407502207	CV3435765	single nucleotide variant	NM_001371116.1(FHDC1):c.124C>G (p.Pro42Ala)	not specified [RCV004623409]	uncertain significance	4	152943181	152943181	Human		name
407502227	CV3435769	single nucleotide variant	NM_001371116.1(FHDC1):c.2109G>A (p.Pro703=)	not specified [RCV004623413]	likely benign	4	152975400	152975400	Human		name
407502237	CV3435771	single nucleotide variant	NM_001371116.1(FHDC1):c.214A>T (p.Ile72Phe)	not specified [RCV004623415]	uncertain significance	4	152943271	152943271	Human		name
15099440	CV698392	single nucleotide variant	NM_001371116.1(FHDC1):c.1260A>G (p.Gln420=)	not provided [RCV000958762]	benign	4	152972418	152972418	Human		name
15184190	CV709196	single nucleotide variant	NM_001371116.1(FHDC1):c.1077G>A (p.Leu359=)	not provided [RCV000975053]	benign	4	152964952	152964952	Human		name
15137792	CV709198	single nucleotide variant	NM_001371116.1(FHDC1):c.1872C>T (p.Ala624=)	not provided [RCV000965680]	benign	4	152975163	152975163	Human		name
15103273	CV720793	single nucleotide variant	NM_001371116.1(FHDC1):c.1995A>T (p.Pro665=)	not provided [RCV000892639]	benign	4	152975286	152975286	Human		name
15186053	CV734491	single nucleotide variant	NM_001371116.1(FHDC1):c.1995A>G (p.Pro665=)	not provided [RCV000908701]\|not specified [RCV004028592]	likely benign	4	152975286	152975286	Human		name
156048935	CV2304466	single nucleotide variant	NM_001371116.1(FHDC1):c.752A>G (p.Tyr251Cys)	not specified [RCV004164558]	uncertain significance	4	152960746	152960746	Human		name
156060336	CV2343769	single nucleotide variant	NM_001371116.1(FHDC1):c.613G>A (p.Gly205Arg)	not specified [RCV004190788]	uncertain significance	4	152954269	152954269	Human		name
329374795	CV2470728	single nucleotide variant	NM_001371116.1(FHDC1):c.938A>G (p.Asn313Ser)	not specified [RCV004275968]	uncertain significance	4	152963039	152963039	Human		name
401878808	CV2754834	single nucleotide variant	NM_001371116.1(FHDC1):c.694G>A (p.Val232Met)	not specified [RCV004341311]	uncertain significance	4	152960595	152960595	Human		name
401893581	CV2765356	single nucleotide variant	NM_001371116.1(FHDC1):c.800C>T (p.Ser267Phe)	not specified [RCV004339863]	uncertain significance	4	152960794	152960794	Human		name
401880262	CV2770015	single nucleotide variant	NM_001371116.1(FHDC1):c.631G>A (p.Glu211Lys)	not specified [RCV004353843]	uncertain significance	4	152954287	152954287	Human		name
401897702	CV2772825	single nucleotide variant	NM_001371116.1(FHDC1):c.590A>G (p.His197Arg)	not specified [RCV004357612]	uncertain significance	4	152954246	152954246	Human		name
405760983	CV3250361	single nucleotide variant	NM_001371116.1(FHDC1):c.521G>A (p.Arg174Gln)	not specified [RCV004394253]	uncertain significance	4	152953521	152953521	Human		name
405760988	CV3250362	single nucleotide variant	NM_001371116.1(FHDC1):c.569G>A (p.Arg190Gln)	not specified [RCV004394254]	likely benign	4	152954225	152954225	Human		name
405760997	CV3250364	single nucleotide variant	NM_001371116.1(FHDC1):c.761G>A (p.Arg254Gln)	not specified [RCV004394256]	uncertain significance	4	152960755	152960755	Human		name
405761002	CV3250365	single nucleotide variant	NM_001371116.1(FHDC1):c.866A>G (p.Glu289Gly)	not specified [RCV004394257]	uncertain significance	4	152962829	152962829	Human		name
407502217	CV3435767	single nucleotide variant	NM_001371116.1(FHDC1):c.689G>A (p.Gly230Asp)	not specified [RCV004623411]	uncertain significance	4	152960590	152960590	Human		name
597752484	CV3669384	single nucleotide variant	NM_001371116.1(FHDC1):c.662A>C (p.Glu221Ala)	not specified [RCV004923933]	uncertain significance	4	152954318	152954318	Human		name
597752494	CV3669386	single nucleotide variant	NM_001371116.1(FHDC1):c.934G>A (p.Gly312Ser)	not specified [RCV004923935]	uncertain significance	4	152963035	152963035	Human		name
597752508	CV3669389	single nucleotide variant	NM_001371116.1(FHDC1):c.503C>A (p.Thr168Asn)	not specified [RCV004923938]	uncertain significance	4	152953503	152953503	Human		name
597752531	CV3669394	single nucleotide variant	NM_001371116.1(FHDC1):c.871C>A (p.Leu291Ile)	not specified [RCV004923943]	uncertain significance	4	152962834	152962834	Human		name
597752543	CV3669397	single nucleotide variant	NM_001371116.1(FHDC1):c.317C>A (p.Pro106Gln)	not specified [RCV004923946]	uncertain significance	4	152943374	152943374	Human		name
597752552	CV3669399	single nucleotide variant	NM_001371116.1(FHDC1):c.962C>T (p.Ser321Phe)	not specified [RCV004923948]	uncertain significance	4	152963063	152963063	Human		name
597752557	CV3669400	single nucleotide variant	NM_001371116.1(FHDC1):c.695T>C (p.Val232Ala)	not specified [RCV004923949]	uncertain significance	4	152960596	152960596	Human		name
597752565	CV3669402	single nucleotide variant	NM_001371116.1(FHDC1):c.574A>T (p.Ile192Phe)	not specified [RCV004923951]	uncertain significance	4	152954230	152954230	Human		name
598242296	CV3955667	single nucleotide variant	NM_001371116.1(FHDC1):c.358G>A (p.Ala120Thr)	not specified [RCV005344501]	uncertain significance	4	152943415	152943415	Human		name
156185141	CV2195541	single nucleotide variant	NM_001371116.1(FHDC1):c.2006G>T (p.Gly669Val)	not specified [RCV004082756]	uncertain significance	4	152975297	152975297	Human		name
155919200	CV2202427	single nucleotide variant	NM_001371116.1(FHDC1):c.2108C>T (p.Pro703Leu)	not provided [RCV004695358]\|not specified [RCV004080736]	uncertain significance	4	152975399	152975399	Human		name
156046665	CV2216101	single nucleotide variant	NM_001371116.1(FHDC1):c.2626A>C (p.Lys876Gln)	not specified [RCV004097115]	uncertain significance	4	152975917	152975917	Human		name
156331967	CV2220604	single nucleotide variant	NM_001371116.1(FHDC1):c.2306C>T (p.Pro769Leu)	not specified [RCV004097790]	uncertain significance	4	152975597	152975597	Human		name
156384226	CV2231025	single nucleotide variant	NM_001371116.1(FHDC1):c.1816G>A (p.Gly606Arg)	not specified [RCV004092475]	uncertain significance	4	152975107	152975107	Human		name
155974881	CV2235785	single nucleotide variant	NM_001371116.1(FHDC1):c.1370A>G (p.Asn457Ser)	not specified [RCV004111910]	uncertain significance	4	152972528	152972528	Human		name
155951551	CV2238810	single nucleotide variant	NM_001371116.1(FHDC1):c.2635A>C (p.Ser879Arg)	not specified [RCV004109729]	uncertain significance	4	152975926	152975926	Human		name
156233754	CV2245288	single nucleotide variant	NM_001371116.1(FHDC1):c.2621C>G (p.Ala874Gly)	not specified [RCV004107050]	uncertain significance	4	152975912	152975912	Human		name
156153317	CV2245513	single nucleotide variant	NM_001371116.1(FHDC1):c.1697A>G (p.Asn566Ser)	not specified [RCV004109285]	uncertain significance	4	152974988	152974988	Human		name
156139363	CV2246845	single nucleotide variant	NM_001371116.1(FHDC1):c.2198G>T (p.Gly733Val)	not specified [RCV004112657]	uncertain significance	4	152975489	152975489	Human		name
156170233	CV2276908	single nucleotide variant	NM_001371116.1(FHDC1):c.2393C>T (p.Pro798Leu)	not specified [RCV004140249]	uncertain significance	4	152975684	152975684	Human		name
156187246	CV2292451	single nucleotide variant	NM_001371116.1(FHDC1):c.1991C>T (p.Ser664Leu)	not specified [RCV004150242]	uncertain significance	4	152975282	152975282	Human		name
156195182	CV2297203	single nucleotide variant	NM_001371116.1(FHDC1):c.1613G>A (p.Arg538His)	not specified [RCV004151090]	uncertain significance	4	152974904	152974904	Human		name
156049433	CV2304503	single nucleotide variant	NM_001371116.1(FHDC1):c.2697C>G (p.Asn899Lys)	not specified [RCV004164586]	uncertain significance	4	152975988	152975988	Human		name
156207664	CV2307996	single nucleotide variant	NM_001371116.1(FHDC1):c.2410G>A (p.Gly804Arg)	not specified [RCV004170428]	uncertain significance	4	152975701	152975701	Human		name
156059335	CV2316973	single nucleotide variant	NM_001371116.1(FHDC1):c.2153G>A (p.Ser718Asn)	not specified [RCV004174473]	uncertain significance	4	152975444	152975444	Human		name
156072040	CV2328679	single nucleotide variant	NM_001371116.1(FHDC1):c.2197G>A (p.Gly733Arg)	not specified [RCV004177919]	uncertain significance	4	152975488	152975488	Human		name
156073996	CV2331625	single nucleotide variant	NM_001371116.1(FHDC1):c.1393G>A (p.Asp465Asn)	not specified [RCV004184260]	uncertain significance	4	152974684	152974684	Human		name
156279076	CV2348299	single nucleotide variant	NM_001371116.1(FHDC1):c.2405G>C (p.Gly802Ala)	not specified [RCV004193499]	uncertain significance	4	152975696	152975696	Human		name
155904369	CV2353853	single nucleotide variant	NM_001371116.1(FHDC1):c.1318A>G (p.Met440Val)	not specified [RCV004201853]	uncertain significance	4	152972476	152972476	Human		name
156121854	CV2354286	single nucleotide variant	NM_001371116.1(FHDC1):c.1601C>G (p.Pro534Arg)	not specified [RCV004206707]	uncertain significance	4	152974892	152974892	Human		name
155902368	CV2356446	single nucleotide variant	NM_001371116.1(FHDC1):c.2668T>G (p.Ser890Ala)	not specified [RCV004206245]	uncertain significance	4	152975959	152975959	Human		name
156102547	CV2363163	single nucleotide variant	NM_001371116.1(FHDC1):c.2581G>C (p.Ala861Pro)	not specified [RCV004213733]	uncertain significance	4	152975872	152975872	Human		name
156213568	CV2367103	single nucleotide variant	NM_001371116.1(FHDC1):c.2437G>A (p.Gly813Arg)	not specified [RCV004215546]	uncertain significance	4	152975728	152975728	Human		name
156213652	CV2367111	single nucleotide variant	NM_001371116.1(FHDC1):c.2236C>T (p.Pro746Ser)	not specified [RCV004215554]	uncertain significance	4	152975527	152975527	Human		name
156385289	CV2368238	single nucleotide variant	NM_001371116.1(FHDC1):c.1618C>T (p.Arg540Cys)	not specified [RCV004219032]	uncertain significance	4	152974909	152974909	Human		name
156070404	CV2381310	single nucleotide variant	NM_001371116.1(FHDC1):c.2389G>T (p.Asp797Tyr)	not specified [RCV004227369]	uncertain significance	4	152975680	152975680	Human		name
155959725	CV2390574	single nucleotide variant	NM_001371116.1(FHDC1):c.1453C>T (p.Arg485Cys)	not specified [RCV004239104]	uncertain significance	4	152974744	152974744	Human		name
155927902	CV2391566	single nucleotide variant	NM_001371116.1(FHDC1):c.2623T>G (p.Ser875Ala)	not specified [RCV004239946]	uncertain significance	4	152975914	152975914	Human		name
156196395	CV2400618	single nucleotide variant	NM_001371116.1(FHDC1):c.1831G>A (p.Ala611Thr)	not specified [RCV004242304]	uncertain significance	4	152975122	152975122	Human		name
329358532	CV2425285	single nucleotide variant	NM_001371116.1(FHDC1):c.2239G>A (p.Asp747Asn)	not specified [RCV004250953]	uncertain significance	4	152975530	152975530	Human		name
329365943	CV2441250	single nucleotide variant	NM_001371116.1(FHDC1):c.1967G>A (p.Gly656Asp)	not specified [RCV004263633]	uncertain significance	4	152975258	152975258	Human		name
329363781	CV2469345	single nucleotide variant	NM_001371116.1(FHDC1):c.2951C>G (p.Pro984Arg)	not specified [RCV004280984]	uncertain significance	4	152976242	152976242	Human		name
329393790	CV2472125	single nucleotide variant	NM_001371116.1(FHDC1):c.1473G>T (p.Glu491Asp)	not specified [RCV004283258]	uncertain significance	4	152974764	152974764	Human		name
401740503	CV2684373	single nucleotide variant	NM_001371116.1(FHDC1):c.1955C>T (p.Pro652Leu)	not specified [RCV004289018]	uncertain significance	4	152975246	152975246	Human		name
401774842	CV2688306	single nucleotide variant	NM_001371116.1(FHDC1):c.2774G>C (p.Arg925Pro)	not specified [RCV004299314]	uncertain significance	4	152976065	152976065	Human		name
401764061	CV2700388	single nucleotide variant	NM_001371116.1(FHDC1):c.2809A>G (p.Thr937Ala)	not specified [RCV004311037]	uncertain significance	4	152976100	152976100	Human		name
401769784	CV2731631	single nucleotide variant	NM_001371116.1(FHDC1):c.2678C>A (p.Thr893Asn)	not specified [RCV004330973]	uncertain significance	4	152975969	152975969	Human		name
401889487	CV2758144	single nucleotide variant	NM_001371116.1(FHDC1):c.2632G>C (p.Gly878Arg)	not specified [RCV004341520]	uncertain significance	4	152975923	152975923	Human		name
401890407	CV2768190	single nucleotide variant	NM_001371116.1(FHDC1):c.2645G>A (p.Arg882Gln)	not specified [RCV004350193]	uncertain significance	4	152975936	152975936	Human		name
401896314	CV2773976	single nucleotide variant	NM_001371116.1(FHDC1):c.2675G>A (p.Arg892Gln)	not specified [RCV004358389]	uncertain significance	4	152975966	152975966	Human		name
401894922	CV2782130	single nucleotide variant	NM_001371116.1(FHDC1):c.1562C>T (p.Pro521Leu)	not specified [RCV004359118]	uncertain significance	4	152974853	152974853	Human		name
401895288	CV2786328	single nucleotide variant	NM_001371116.1(FHDC1):c.2849C>A (p.Thr950Lys)	not specified [RCV004361934]	uncertain significance	4	152976140	152976140	Human		name
405760869	CV3250342	single nucleotide variant	NM_001371116.1(FHDC1):c.1193G>A (p.Cys398Tyr)	not specified [RCV004394234]	uncertain significance	4	152968072	152968072	Human		name
405760875	CV3250343	single nucleotide variant	NM_001371116.1(FHDC1):c.1397G>A (p.Arg466Gln)	not specified [RCV004394235]	uncertain significance	4	152974688	152974688	Human		name
405760881	CV3250344	single nucleotide variant	NM_001371116.1(FHDC1):c.1601C>T (p.Pro534Leu)	not specified [RCV004394236]	uncertain significance	4	152974892	152974892	Human		name
405760887	CV3250345	single nucleotide variant	NM_001371116.1(FHDC1):c.1627C>A (p.Leu543Met)	not specified [RCV004394237]	uncertain significance	4	152974918	152974918	Human		name
405760894	CV3250346	single nucleotide variant	NM_001371116.1(FHDC1):c.1637C>T (p.Ser546Phe)	not specified [RCV004394238]	uncertain significance	4	152974928	152974928	Human		name
405760905	CV3250348	single nucleotide variant	NM_001371116.1(FHDC1):c.1877A>T (p.Gln626Leu)	not specified [RCV004394240]	uncertain significance	4	152975168	152975168	Human		name
405760911	CV3250349	single nucleotide variant	NM_001371116.1(FHDC1):c.1973C>G (p.Ala658Gly)	not specified [RCV004394241]	uncertain significance	4	152975264	152975264	Human		name
405760917	CV3250350	single nucleotide variant	NM_001371116.1(FHDC1):c.2056G>T (p.Gly686Cys)	not specified [RCV004394242]	uncertain significance	4	152975347	152975347	Human		name
405760923	CV3250351	single nucleotide variant	NM_001371116.1(FHDC1):c.2181G>A (p.Met727Ile)	not specified [RCV004394243]	uncertain significance	4	152975472	152975472	Human		name
405760929	CV3250352	single nucleotide variant	NM_001371116.1(FHDC1):c.2336G>A (p.Cys779Tyr)	not specified [RCV004394244]	uncertain significance	4	152975627	152975627	Human		name
407502197	CV3435763	single nucleotide variant	NM_001371116.1(FHDC1):c.2974C>A (p.Leu992Ile)	not specified [RCV004623407]	uncertain significance	4	152976265	152976265	Human		name
407502203	CV3435764	single nucleotide variant	NM_001371116.1(FHDC1):c.1658C>T (p.Thr553Ile)	not specified [RCV004623408]	uncertain significance	4	152974949	152974949	Human		name
407502213	CV3435766	single nucleotide variant	NM_001371116.1(FHDC1):c.1457C>G (p.Ser486Cys)	not specified [RCV004623410]	uncertain significance	4	152974748	152974748	Human		name
407502223	CV3435768	single nucleotide variant	NM_001371116.1(FHDC1):c.1532G>C (p.Gly511Ala)	not specified [RCV004623412]	uncertain significance	4	152974823	152974823	Human		name
407502232	CV3435770	single nucleotide variant	NM_001371116.1(FHDC1):c.2260T>A (p.Leu754Met)	not specified [RCV004623414]	uncertain significance	4	152975551	152975551	Human		name
407502242	CV3435772	single nucleotide variant	NM_001371116.1(FHDC1):c.2284C>T (p.Pro762Ser)	not specified [RCV004623416]	uncertain significance	4	152975575	152975575	Human		name
597752468	CV3669381	single nucleotide variant	NM_001371116.1(FHDC1):c.1747A>G (p.Ile583Val)	not specified [RCV004923930]	likely benign	4	152975038	152975038	Human		name
597752474	CV3669382	single nucleotide variant	NM_001371116.1(FHDC1):c.2718G>A (p.Met906Ile)	not specified [RCV004923931]	uncertain significance	4	152976009	152976009	Human		name
597752479	CV3669383	single nucleotide variant	NM_001371116.1(FHDC1):c.1863G>T (p.Gln621His)	not specified [RCV004923932]	uncertain significance	4	152975154	152975154	Human		name
597752503	CV3669388	single nucleotide variant	NM_001371116.1(FHDC1):c.2384G>A (p.Gly795Asp)	not specified [RCV004923937]	uncertain significance	4	152975675	152975675	Human		name
597752512	CV3669390	single nucleotide variant	NM_001371116.1(FHDC1):c.2012A>T (p.Lys671Met)	not specified [RCV004923939]	uncertain significance	4	152975303	152975303	Human		name
597752516	CV3669391	single nucleotide variant	NM_001371116.1(FHDC1):c.1739G>A (p.Arg580Gln)	not specified [RCV004923940]	uncertain significance	4	152975030	152975030	Human		name
597752521	CV3669392	single nucleotide variant	NM_001371116.1(FHDC1):c.2281G>A (p.Asp761Asn)	not specified [RCV004923941]	uncertain significance	4	152975572	152975572	Human		name
597752525	CV3669393	single nucleotide variant	NM_001371116.1(FHDC1):c.2071G>A (p.Glu691Lys)	not specified [RCV004923942]	uncertain significance	4	152975362	152975362	Human		name
597752537	CV3669395	single nucleotide variant	NM_001371116.1(FHDC1):c.1766C>A (p.Ala589Glu)	not specified [RCV004923944]	likely benign	4	152975057	152975057	Human		name
597752562	CV3669401	single nucleotide variant	NM_001371116.1(FHDC1):c.1594C>T (p.Arg532Trp)	not specified [RCV004923950]	uncertain significance	4	152974885	152974885	Human		name
597752570	CV3669403	single nucleotide variant	NM_001371116.1(FHDC1):c.2321C>G (p.Ser774Trp)	not specified [RCV004923952]	uncertain significance	4	152975612	152975612	Human		name
597752574	CV3669404	single nucleotide variant	NM_001371116.1(FHDC1):c.1223C>T (p.Ala408Val)	not specified [RCV004923953]	uncertain significance	4	152972381	152972381	Human		name
597752579	CV3669405	single nucleotide variant	NM_001371116.1(FHDC1):c.2308C>G (p.Leu770Val)	not specified [RCV004923954]	uncertain significance	4	152975599	152975599	Human		name
597752584	CV3669406	single nucleotide variant	NM_001371116.1(FHDC1):c.2978C>G (p.Pro993Arg)	not specified [RCV004923955]	uncertain significance	4	152976269	152976269	Human		name
598242249	CV3955658	single nucleotide variant	NM_001371116.1(FHDC1):c.1916G>A (p.Arg639His)	not specified [RCV005344493]	likely benign	4	152975207	152975207	Human		name
598242255	CV3955659	single nucleotide variant	NM_001371116.1(FHDC1):c.2003T>C (p.Leu668Pro)	not specified [RCV005344494]	uncertain significance	4	152975294	152975294	Human		name
598242261	CV3955660	single nucleotide variant	NM_001371116.1(FHDC1):c.2857G>A (p.Glu953Lys)	not specified [RCV005344495]	uncertain significance	4	152976148	152976148	Human		name
598242266	CV3955662	single nucleotide variant	NM_001371116.1(FHDC1):c.1873G>A (p.Ala625Thr)	not specified [RCV005344496]	uncertain significance	4	152975164	152975164	Human		name
598242279	CV3955664	single nucleotide variant	NM_001371116.1(FHDC1):c.1290A>G (p.Ile430Met)	not specified [RCV005344498]	uncertain significance	4	152972448	152972448	Human		name
598242285	CV3955665	single nucleotide variant	NM_001371116.1(FHDC1):c.2773C>G (p.Arg925Gly)	not specified [RCV005344499]	uncertain significance	4	152976064	152976064	Human		name
598242291	CV3955666	single nucleotide variant	NM_001371116.1(FHDC1):c.1979C>A (p.Ser660Tyr)	not specified [RCV005344500]	uncertain significance	4	152975270	152975270	Human		name
598242301	CV3955668	single nucleotide variant	NM_001371116.1(FHDC1):c.2667G>T (p.Lys889Asn)	not specified [RCV005344502]	uncertain significance	4	152975958	152975958	Human		name
598242307	CV3955669	single nucleotide variant	NM_001371116.1(FHDC1):c.2552A>G (p.Asp851Gly)	not specified [RCV005344503]	uncertain significance	4	152975843	152975843	Human		name
598242312	CV3955670	single nucleotide variant	NM_001371116.1(FHDC1):c.2817G>T (p.Trp939Cys)	not specified [RCV005344504]	uncertain significance	4	152976108	152976108	Human		name
598272104	CV3955671	single nucleotide variant	NM_001371116.1(FHDC1):c.2663C>T (p.Ala888Val)	not specified [RCV005327890]	uncertain significance	4	152975954	152975954	Human		name
15186205	CV698393	single nucleotide variant	NM_001371116.1(FHDC1):c.2539G>A (p.Gly847Ser)	not provided [RCV000953214]	benign	4	152975830	152975830	Human		name
15133556	CV709197	single nucleotide variant	NM_001371116.1(FHDC1):c.1543C>A (p.Leu515Met)	not provided [RCV000964972]	benign	4	152974834	152974834	Human		name
15155511	CV720792	single nucleotide variant	NM_001371116.1(FHDC1):c.1856C>A (p.Ala619Glu)	not provided [RCV000880432]	benign	4	152975147	152975147	Human		name
15155516	CV720794	single nucleotide variant	NM_001371116.1(FHDC1):c.2200A>T (p.Ser734Cys)	not provided [RCV000880433]	benign	4	152975491	152975491	Human		name
15129383	CV748771	single nucleotide variant	NM_001371116.1(FHDC1):c.2248G>A (p.Gly750Arg)	not provided [RCV000919820]	likely benign	4	152975539	152975539	Human		name
156234078	CV2271066	single nucleotide variant	NM_001371116.1(FHDC1):c.3041A>C (p.Lys1014Thr)	not specified [RCV004134457]	uncertain significance	4	152976332	152976332	Human		name
155900775	CV2275260	single nucleotide variant	NM_001371116.1(FHDC1):c.3355G>A (p.Gly1119Arg)	not specified [RCV004137042]	uncertain significance	4	152976646	152976646	Human		name
155931180	CV2362483	single nucleotide variant	NM_001371116.1(FHDC1):c.3073G>A (p.Val1025Ile)	not specified [RCV004213104]	likely benign	4	152976364	152976364	Human		name
155936180	CV2380321	single nucleotide variant	NM_001371116.1(FHDC1):c.3374G>A (p.Arg1125His)	not specified [RCV004224668]	uncertain significance	4	152976665	152976665	Human		name
329386289	CV2428241	single nucleotide variant	NM_001371116.1(FHDC1):c.3245A>T (p.Asp1082Val)	not specified [RCV004251272]	uncertain significance	4	152976536	152976536	Human		name
401867018	CV2759072	single nucleotide variant	NM_001371116.1(FHDC1):c.3376C>G (p.Arg1126Gly)	not specified [RCV004342376]	uncertain significance	4	152976667	152976667	Human		name
405760946	CV3250355	single nucleotide variant	NM_001371116.1(FHDC1):c.3068C>G (p.Pro1023Arg)	not specified [RCV004394247]	uncertain significance	4	152976359	152976359	Human		name
405760952	CV3250356	single nucleotide variant	NM_001371116.1(FHDC1):c.3200G>A (p.Arg1067Gln)	not specified [RCV004394248]	uncertain significance	4	152976491	152976491	Human		name
405760958	CV3250357	single nucleotide variant	NM_001371116.1(FHDC1):c.3352G>A (p.Ala1118Thr)	not specified [RCV004394249]	uncertain significance	4	152976643	152976643	Human		name
405760964	CV3250358	single nucleotide variant	NM_001371116.1(FHDC1):c.3353C>G (p.Ala1118Gly)	not specified [RCV004394250]	uncertain significance	4	152976644	152976644	Human		name
405760975	CV3250360	single nucleotide variant	NM_001371116.1(FHDC1):c.3416A>G (p.Asn1139Ser)	not specified [RCV004394252]	uncertain significance	4	152976707	152976707	Human		name
597752463	CV3669380	single nucleotide variant	NM_001371116.1(FHDC1):c.3263G>T (p.Arg1088Leu)	not specified [RCV004923929]	uncertain significance	4	152976554	152976554	Human		name
597752489	CV3669385	single nucleotide variant	NM_001371116.1(FHDC1):c.3218G>A (p.Gly1073Glu)	not specified [RCV004923934]	uncertain significance	4	152976509	152976509	Human		name
597752539	CV3669396	single nucleotide variant	NM_001371116.1(FHDC1):c.3045A>C (p.Glu1015Asp)	not specified [RCV004923945]	uncertain significance	4	152976336	152976336	Human		name
598242232	CV3955655	single nucleotide variant	NM_001371116.1(FHDC1):c.3082G>C (p.Glu1028Gln)	not specified [RCV005344490]	uncertain significance	4	152976373	152976373	Human		name
598242244	CV3955657	single nucleotide variant	NM_001371116.1(FHDC1):c.3277C>T (p.Arg1093Trp)	not specified [RCV005344492]	uncertain significance	4	152976568	152976568	Human		name
598272099	CV3955661	single nucleotide variant	NM_001371116.1(FHDC1):c.3007T>G (p.Cys1003Gly)	not specified [RCV005327889]	uncertain significance	4	152976298	152976298	Human		name
15099448	CV698394	single nucleotide variant	NM_001371116.1(FHDC1):c.3247A>G (p.Ser1083Gly)	not provided [RCV000958763]	benign	4	152976538	152976538	Human		name

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