Stard13 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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123 records found for search term Stard13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582779	CV117335	single nucleotide variant	NM_178006.3(STARD13):c.170-35549G>A	Lung cancer [RCV000097856]	uncertain significance	13	33203171	33203171	Human		name
8582780	CV117336	single nucleotide variant	NM_178006.3(STARD13):c.169+48719C>T	Lung cancer [RCV000097857]	uncertain significance	13	33236751	33236751	Human		name
8582782	CV117338	single nucleotide variant	NM_001243476.2(STARD13):c.-421+706C>G	Lung cancer [RCV000097859]	uncertain significance	13	33675972	33675972	Human		name
8582781	CV117337	single nucleotide variant	NM_001243476.2(STARD13):c.-105-61478C>A	Lung cancer [RCV000097858]	uncertain significance	13	33585850	33585850	Human		name
15197689	CV725472	single nucleotide variant	NM_178006.4(STARD13):c.237T>C (p.Tyr79=)	not provided [RCV000890134]	benign	13	33167555	33167555	Human		name
156014988	CV2269741	single nucleotide variant	NM_178006.4(STARD13):c.47T>A (p.Leu16Gln)	not specified [RCV004126991]	uncertain significance	13	33285592	33285592	Human		name
156048812	CV2336472	single nucleotide variant	NM_178006.4(STARD13):c.56T>C (p.Met19Thr)	not specified [RCV004194684]	uncertain significance	13	33285583	33285583	Human		name
155939504	CV2385685	single nucleotide variant	NM_178006.4(STARD13):c.77T>C (p.Met26Thr)	not specified [RCV004233312]	uncertain significance	13	33285562	33285562	Human		name
329363226	CV2464977	single nucleotide variant	NM_178006.4(STARD13):c.71A>G (p.Gln24Arg)	not specified [RCV004284893]	uncertain significance	13	33285568	33285568	Human		name
401901821	CV2813822	single nucleotide variant	NM_178006.4(STARD13):c.750G>A (p.Lys250=)	not provided [RCV003393256]	likely benign	13	33129927	33129927	Human		name
598213884	CV3919407	single nucleotide variant	NM_178006.4(STARD13):c.83T>C (p.Leu28Ser)	not specified [RCV005271089]	uncertain significance	13	33285556	33285556	Human		name
15199885	CV702674	single nucleotide variant	NM_178006.4(STARD13):c.495A>T (p.Arg165=)	not provided [RCV000957171]	benign	13	33130182	33130182	Human		name
15193817	CV702675	single nucleotide variant	NM_178006.4(STARD13):c.468G>A (p.Val156=)	not provided [RCV000955478]	benign	13	33130209	33130209	Human		name
8627440	CV82584	single nucleotide variant	NM_178006.4(STARD13):c.696C>T (p.Leu232=)	not provided [RCV000926747]	likely benign\|not provided	13	33129981	33129981	Human		name
156256736	CV2204529	single nucleotide variant	NM_178006.4(STARD13):c.142C>A (p.His48Asn)	not specified [RCV004081648]	uncertain significance	13	33285497	33285497	Human		name
401901820	CV2813821	single nucleotide variant	NM_178006.4(STARD13):c.1344G>A (p.Ala448=)	not provided [RCV003393255]	likely benign	13	33129333	33129333	Human		name
405722559	CV3323752	single nucleotide variant	NM_178006.4(STARD13):c.106C>T (p.Arg36Cys)	not specified [RCV004463353]	uncertain significance	13	33285533	33285533	Human		name
407530077	CV3485304	single nucleotide variant	NM_178006.4(STARD13):c.179C>T (p.Ala60Val)	not specified [RCV004681618]	uncertain significance	13	33167613	33167613	Human		name
407530079	CV3485307	single nucleotide variant	NM_178006.4(STARD13):c.1875G>A (p.Thr625=)	not specified [RCV004681620]	likely benign	13	33127420	33127420	Human		name
597682656	CV3618386	single nucleotide variant	NM_178006.4(STARD13):c.226G>A (p.Ala76Thr)	not specified [RCV004857669]	uncertain significance	13	33167566	33167566	Human		name
597746743	CV3618388	single nucleotide variant	NM_178006.4(STARD13):c.263T>C (p.Ile88Thr)	not specified [RCV004865934]	uncertain significance	13	33165397	33165397	Human		name
598250437	CV3919409	single nucleotide variant	NM_178006.4(STARD13):c.104G>A (p.Arg35Lys)	not specified [RCV005277715]	uncertain significance	13	33285535	33285535	Human		name
15199881	CV702672	single nucleotide variant	NM_178006.4(STARD13):c.1275T>C (p.Asn425=)	not provided [RCV000957170]	benign	13	33129402	33129402	Human		name
15193813	CV702673	single nucleotide variant	NM_178006.4(STARD13):c.1116G>T (p.Gly372=)	not provided [RCV000955477]	benign	13	33129561	33129561	Human		name
15152019	CV713911	single nucleotide variant	NM_178006.4(STARD13):c.2790G>A (p.Thr930=)	not provided [RCV000968265]	benign	13	33110725	33110725	Human		name
15154188	CV739033	single nucleotide variant	NM_178006.4(STARD13):c.2889C>T (p.Pro963=)	not provided [RCV000901906]	benign	13	33110031	33110031	Human		name
15150605	CV739034	single nucleotide variant	NM_178006.4(STARD13):c.2310C>T (p.Ala770=)	not provided [RCV000901190]	benign	13	33112903	33112903	Human		name
15183147	CV739035	single nucleotide variant	NM_178006.4(STARD13):c.1062C>T (p.His354=)	not provided [RCV000907995]	benign	13	33129615	33129615	Human		name
15124814	CV753818	single nucleotide variant	NM_178006.4(STARD13):c.1113G>A (p.Ala371=)	not provided [RCV000919045]	likely benign	13	33129564	33129564	Human		name
156244722	CV2243182	single nucleotide variant	NM_178006.4(STARD13):c.469G>T (p.Asp157Tyr)	not specified [RCV004110077]	uncertain significance	13	33130208	33130208	Human		name
155995433	CV2250347	single nucleotide variant	NM_178006.4(STARD13):c.408A>T (p.Glu136Asp)	not specified [RCV004127237]	uncertain significance	13	33130269	33130269	Human		name
156071455	CV2251413	single nucleotide variant	NM_178006.4(STARD13):c.602A>G (p.Glu201Gly)	not specified [RCV004117395]	uncertain significance	13	33130075	33130075	Human		name
156278201	CV2284912	single nucleotide variant	NM_178006.4(STARD13):c.539C>T (p.Thr180Met)	not specified [RCV004143360]	uncertain significance	13	33130138	33130138	Human		name
156286876	CV2288345	single nucleotide variant	NM_178006.4(STARD13):c.734A>G (p.His245Arg)	not specified [RCV004150114]	uncertain significance	13	33129943	33129943	Human		name
156085738	CV2295276	single nucleotide variant	NM_178006.4(STARD13):c.827A>G (p.Lys276Arg)	not specified [RCV004158649]	uncertain significance	13	33129850	33129850	Human		name
156146548	CV2357942	single nucleotide variant	NM_178006.4(STARD13):c.622A>T (p.Ser208Cys)	not specified [RCV004209725]	uncertain significance	13	33130055	33130055	Human		name
156402777	CV2371595	single nucleotide variant	NM_178006.4(STARD13):c.659C>T (p.Pro220Leu)	not specified [RCV004216842]	uncertain significance	13	33130018	33130018	Human		name
155903707	CV2386588	single nucleotide variant	NM_178006.4(STARD13):c.482C>T (p.Thr161Met)	not specified [RCV004230938]	uncertain significance	13	33130195	33130195	Human		name
329371560	CV2432012	single nucleotide variant	NM_178006.4(STARD13):c.784C>T (p.Arg262Cys)	not specified [RCV004249164]	uncertain significance	13	33129893	33129893	Human		name
329398321	CV2464445	single nucleotide variant	NM_178006.4(STARD13):c.400G>A (p.Asp134Asn)	not specified [RCV004276368]	uncertain significance	13	33130277	33130277	Human		name
401739014	CV2722033	single nucleotide variant	NM_178006.4(STARD13):c.869T>C (p.Met290Thr)	not specified [RCV004326518]	uncertain significance	13	33129808	33129808	Human		name
401743943	CV2722187	single nucleotide variant	NM_178006.4(STARD13):c.989G>A (p.Ser330Asn)	not specified [RCV004328754]	uncertain significance	13	33129688	33129688	Human		name
597746728	CV3618382	single nucleotide variant	NM_178006.4(STARD13):c.656A>G (p.Asn219Ser)	not specified [RCV004865931]	likely benign	13	33130021	33130021	Human		name
597746733	CV3618383	single nucleotide variant	NM_178006.4(STARD13):c.884C>T (p.Pro295Leu)	not specified [RCV004865932]	uncertain significance	13	33129793	33129793	Human		name
597746738	CV3618385	single nucleotide variant	NM_178006.4(STARD13):c.800G>A (p.Arg267Gln)	not specified [RCV004865933]	uncertain significance	13	33129877	33129877	Human		name
597682678	CV3618389	single nucleotide variant	NM_178006.4(STARD13):c.439C>G (p.Gln147Glu)	not specified [RCV004857671]	uncertain significance	13	33130238	33130238	Human		name
597682699	CV3618391	single nucleotide variant	NM_178006.4(STARD13):c.816C>A (p.His272Gln)	not specified [RCV004857673]	uncertain significance	13	33129861	33129861	Human		name
598250424	CV3919406	single nucleotide variant	NM_178006.4(STARD13):c.394G>T (p.Asp132Tyr)	not specified [RCV005277713]	uncertain significance	13	33130283	33130283	Human		name
15182200	CV713909	single nucleotide variant	NM_178006.4(STARD13):c.3174G>A (p.Pro1058=)	not provided [RCV000974575]	benign\|likely benign	13	33106808	33106808	Human		name
15114082	CV753819	single nucleotide variant	NM_178006.4(STARD13):c.466G>A (p.Val156Met)	not provided [RCV000917210]	likely benign	13	33130211	33130211	Human		name
8635022	CV90244	single nucleotide variant	NM_178006.3(STARD13):c.3099C>G (p.Ser1033=)	Malignant melanoma [RCV000070342]	not provided	13	33106883	33106883	Human		name
156319587	CV2200552	single nucleotide variant	NM_178006.4(STARD13):c.1076G>A (p.Arg359His)	not specified [RCV004078900]	uncertain significance	13	33129601	33129601	Human		name
156139897	CV2202937	single nucleotide variant	NM_178006.4(STARD13):c.1634G>A (p.Arg545Gln)	not specified [RCV004069204]	uncertain significance	13	33129043	33129043	Human		name
155927365	CV2230774	single nucleotide variant	NM_178006.4(STARD13):c.1759T>C (p.Trp587Arg)	not specified [RCV004091993]	uncertain significance	13	33127536	33127536	Human		name
155952659	CV2264254	single nucleotide variant	NM_178006.4(STARD13):c.1874C>T (p.Thr625Met)	not specified [RCV004138182]	uncertain significance	13	33127421	33127421	Human		name
155906717	CV2279384	single nucleotide variant	NM_178006.4(STARD13):c.1985G>C (p.Gly662Ala)	not specified [RCV004141937]	uncertain significance	13	33126178	33126178	Human		name
156279910	CV2285129	single nucleotide variant	NM_178006.4(STARD13):c.1793C>G (p.Pro598Arg)	not specified [RCV004145351]	uncertain significance	13	33127502	33127502	Human		name
156252113	CV2286929	single nucleotide variant	NM_178006.4(STARD13):c.2419C>T (p.Pro807Ser)	not specified [RCV004144536]	uncertain significance	13	33112794	33112794	Human		name
156396590	CV2322463	single nucleotide variant	NM_178006.4(STARD13):c.1844T>C (p.Leu615Pro)	not specified [RCV004180584]	uncertain significance	13	33127451	33127451	Human		name
156300920	CV2322617	single nucleotide variant	NM_178006.4(STARD13):c.2762C>T (p.Ala921Val)	not specified [RCV004182754]	uncertain significance	13	33110753	33110753	Human		name
156352904	CV2324069	single nucleotide variant	NM_178006.4(STARD13):c.1405G>T (p.Ala469Ser)	not specified [RCV004178364]	uncertain significance	13	33129272	33129272	Human		name
156395885	CV2325980	single nucleotide variant	NM_178006.4(STARD13):c.1574C>T (p.Thr525Ile)	not specified [RCV004176192]	uncertain significance	13	33129103	33129103	Human		name
156174680	CV2326980	single nucleotide variant	NM_178006.4(STARD13):c.1757G>A (p.Arg586Gln)	not specified [RCV004176787]	uncertain significance	13	33127538	33127538	Human		name
156059491	CV2343710	single nucleotide variant	NM_178006.4(STARD13):c.1846C>T (p.Leu616Phe)	not specified [RCV004190734]	uncertain significance	13	33127449	33127449	Human		name
156062261	CV2353749	single nucleotide variant	NM_178006.4(STARD13):c.1342G>A (p.Ala448Thr)	not specified [RCV004201758]	uncertain significance	13	33129335	33129335	Human		name
156131446	CV2358265	single nucleotide variant	NM_178006.4(STARD13):c.1789C>T (p.Arg597Trp)	not specified [RCV004212053]	uncertain significance	13	33127506	33127506	Human		name
155928743	CV2369557	single nucleotide variant	NM_178006.4(STARD13):c.1012C>A (p.His338Asn)	not specified [RCV004214976]	likely benign	13	33129665	33129665	Human		name
156184072	CV2377686	single nucleotide variant	NM_178006.4(STARD13):c.1940T>C (p.Met647Thr)	not specified [RCV004228232]	uncertain significance	13	33126223	33126223	Human		name
156391840	CV2382642	single nucleotide variant	NM_178006.4(STARD13):c.1867C>T (p.Arg623Cys)	not specified [RCV004232964]	uncertain significance	13	33127428	33127428	Human		name
156039193	CV2384244	single nucleotide variant	NM_178006.4(STARD13):c.1751G>A (p.Arg584Gln)	not specified [RCV004227634]	uncertain significance	13	33127544	33127544	Human		name
155930291	CV2398367	single nucleotide variant	NM_178006.4(STARD13):c.2423T>C (p.Met808Thr)	not specified [RCV004237705]	uncertain significance	13	33112790	33112790	Human		name
156003199	CV2399636	single nucleotide variant	NM_178006.4(STARD13):c.1633C>T (p.Arg545Trp)	not specified [RCV004244152]	uncertain significance	13	33129044	33129044	Human		name
156103425	CV2400209	single nucleotide variant	NM_178006.4(STARD13):c.2095C>T (p.Arg699Cys)	not specified [RCV004243003]	uncertain significance	13	33118251	33118251	Human		name
329389746	CV2445358	single nucleotide variant	NM_178006.4(STARD13):c.1624T>G (p.Ser542Ala)	not specified [RCV004263973]	uncertain significance	13	33129053	33129053	Human		name
329401627	CV2457235	single nucleotide variant	NM_178006.4(STARD13):c.1930C>T (p.Pro644Ser)	not specified [RCV004265305]	uncertain significance	13	33126233	33126233	Human		name
329395398	CV2458327	single nucleotide variant	NM_178006.4(STARD13):c.1146C>A (p.Ser382Arg)	not specified [RCV004265970]	uncertain significance	13	33129531	33129531	Human		name
329353211	CV2468939	single nucleotide variant	NM_178006.4(STARD13):c.2219G>A (p.Arg740Gln)	not specified [RCV004274206]	uncertain significance	13	33118127	33118127	Human		name
401769437	CV2689744	single nucleotide variant	NM_178006.4(STARD13):c.2195C>T (p.Ala732Val)	not specified [RCV004297655]	uncertain significance	13	33118151	33118151	Human		name
401758726	CV2694246	single nucleotide variant	NM_178006.4(STARD13):c.1594A>G (p.Ile532Val)	not specified [RCV004302660]	uncertain significance	13	33129083	33129083	Human		name
401742942	CV2697974	single nucleotide variant	NM_178006.4(STARD13):c.1007C>T (p.Ser336Leu)	not specified [RCV004302461]	uncertain significance	13	33129670	33129670	Human		name
401717759	CV2704004	single nucleotide variant	NM_178006.4(STARD13):c.1675A>G (p.Asn559Asp)	not specified [RCV004308896]	uncertain significance	13	33129002	33129002	Human		name
401757583	CV2707861	single nucleotide variant	NM_178006.4(STARD13):c.1004C>T (p.Pro335Leu)	not specified [RCV004309139]	uncertain significance	13	33129673	33129673	Human		name
401781051	CV2726409	single nucleotide variant	NM_178006.4(STARD13):c.2975G>A (p.Arg992Lys)	not specified [RCV004328621]	likely benign	13	33109945	33109945	Human		name
401764941	CV2728152	single nucleotide variant	NM_178006.4(STARD13):c.1577T>C (p.Phe526Ser)	not specified [RCV004324201]	uncertain significance	13	33129100	33129100	Human		name
401856145	CV2764411	single nucleotide variant	NM_178006.4(STARD13):c.2968C>G (p.Leu990Val)	not specified [RCV004338981]	uncertain significance	13	33109952	33109952	Human		name
401878006	CV2786933	single nucleotide variant	NM_178006.4(STARD13):c.1580C>T (p.Pro527Leu)	not specified [RCV004366070]	uncertain significance	13	33129097	33129097	Human		name
405722569	CV3323753	single nucleotide variant	NM_178006.4(STARD13):c.1313T>C (p.Val438Ala)	not specified [RCV004463354]	uncertain significance	13	33129364	33129364	Human		name
405722580	CV3323754	single nucleotide variant	NM_178006.4(STARD13):c.1333C>T (p.Arg445Trp)	not specified [RCV004463355]	uncertain significance	13	33129344	33129344	Human		name
405722588	CV3323755	single nucleotide variant	NM_178006.4(STARD13):c.1532T>C (p.Leu511Pro)	not specified [RCV004463356]	uncertain significance	13	33129145	33129145	Human		name
405722594	CV3323756	single nucleotide variant	NM_178006.4(STARD13):c.2293G>C (p.Glu765Gln)	not specified [RCV004463357]	uncertain significance	13	33112920	33112920	Human		name
405722605	CV3323757	single nucleotide variant	NM_178006.4(STARD13):c.2383G>C (p.Asp795His)	not specified [RCV004463358]	uncertain significance	13	33112830	33112830	Human		name
405722617	CV3323759	single nucleotide variant	NM_178006.4(STARD13):c.2489C>T (p.Pro830Leu)	not specified [RCV004463360]	uncertain significance	13	33112724	33112724	Human		name
405722626	CV3323760	single nucleotide variant	NM_178006.4(STARD13):c.2921G>A (p.Arg974His)	not specified [RCV004463361]	uncertain significance	13	33109999	33109999	Human		name
407530078	CV3485305	single nucleotide variant	NM_178006.4(STARD13):c.2789C>T (p.Thr930Met)	not specified [RCV004681619]	uncertain significance	13	33110726	33110726	Human		name
407495781	CV3485306	single nucleotide variant	NM_178006.4(STARD13):c.1561C>T (p.Pro521Ser)	not specified [RCV004667960]	uncertain significance	13	33129116	33129116	Human		name
407530080	CV3485308	single nucleotide variant	NM_178006.4(STARD13):c.2386G>A (p.Val796Ile)	not specified [RCV004681621]	uncertain significance	13	33112827	33112827	Human		name
407530081	CV3485309	single nucleotide variant	NM_178006.4(STARD13):c.2495T>A (p.Val832Asp)	not specified [RCV004681622]	uncertain significance	13	33111890	33111890	Human		name
407495786	CV3485310	single nucleotide variant	NM_178006.4(STARD13):c.1069A>G (p.Asn357Asp)	not specified [RCV004667961]	uncertain significance	13	33129608	33129608	Human		name
597682667	CV3618387	single nucleotide variant	NM_178006.4(STARD13):c.1954G>T (p.Val652Phe)	not specified [RCV004857670]	uncertain significance	13	33126209	33126209	Human		name
597682709	CV3618392	single nucleotide variant	NM_178006.4(STARD13):c.2444C>G (p.Ala815Gly)	not specified [RCV004857674]	uncertain significance	13	33112769	33112769	Human		name
598250399	CV3919402	single nucleotide variant	NM_178006.4(STARD13):c.1019G>A (p.Ser340Asn)	not specified [RCV005277710]	uncertain significance	13	33129658	33129658	Human		name
598250407	CV3919403	single nucleotide variant	NM_178006.4(STARD13):c.2809A>G (p.Thr937Ala)	not specified [RCV005277711]	uncertain significance	13	33110706	33110706	Human		name
598250416	CV3919404	single nucleotide variant	NM_178006.4(STARD13):c.1319G>A (p.Gly440Asp)	not specified [RCV005277712]	uncertain significance	13	33129358	33129358	Human		name
598213889	CV3919405	single nucleotide variant	NM_178006.4(STARD13):c.1772A>C (p.Gln591Pro)	not specified [RCV005271088]	uncertain significance	13	33127523	33127523	Human		name
598213879	CV3919410	single nucleotide variant	NM_178006.4(STARD13):c.2545G>A (p.Glu849Lys)	not specified [RCV005271090]	uncertain significance	13	33111840	33111840	Human		name
598213874	CV3919411	single nucleotide variant	NM_178006.4(STARD13):c.2300G>A (p.Arg767Gln)	not specified [RCV005271091]	uncertain significance	13	33112913	33112913	Human		name
598250445	CV3919412	single nucleotide variant	NM_178006.4(STARD13):c.2153C>G (p.Pro718Arg)	not specified [RCV005277716]	uncertain significance	13	33118193	33118193	Human		name
598250453	CV3919413	single nucleotide variant	NM_178006.4(STARD13):c.1099C>G (p.Leu367Val)	not specified [RCV005277717]	uncertain significance	13	33129578	33129578	Human		name
15185150	CV725471	single nucleotide variant	NM_178006.4(STARD13):c.1112C>T (p.Ala371Val)	not provided [RCV000886617]	likely benign	13	33129565	33129565	Human		name
8635023	CV90245	single nucleotide variant	NM_178006.4(STARD13):c.2935G>A (p.Glu979Lys)	not specified [RCV004463362]	uncertain significance\|not provided	13	33109985	33109985	Human		name
8635024	CV90246	single nucleotide variant	NM_178006.3(STARD13):c.1462G>A (p.Asp488Asn)	Malignant melanoma [RCV000070344]	not provided	13	33129215	33129215	Human		name
156338940	CV2271348	single nucleotide variant	NM_178006.4(STARD13):c.3032A>C (p.Asp1011Ala)	not specified [RCV004136463]	uncertain significance	13	33109888	33109888	Human		name
156248006	CV2357101	single nucleotide variant	NM_178006.4(STARD13):c.3017C>T (p.Pro1006Leu)	not specified [RCV004206900]	uncertain significance	13	33109903	33109903	Human		name
329361564	CV2437647	single nucleotide variant	NM_178006.4(STARD13):c.3158A>G (p.Gln1053Arg)	not specified [RCV004260965]	uncertain significance	13	33106824	33106824	Human		name
401743133	CV2694062	single nucleotide variant	NM_178006.4(STARD13):c.3274G>A (p.Ala1092Thr)	not specified [RCV004302497]	uncertain significance	13	33105661	33105661	Human		name
401740211	CV2705916	single nucleotide variant	NM_178006.4(STARD13):c.3215T>C (p.Ile1072Thr)	not specified [RCV004320844]	uncertain significance	13	33106767	33106767	Human		name
401752374	CV2706988	single nucleotide variant	NM_178006.4(STARD13):c.3120G>C (p.Gln1040His)	not specified [RCV004321586]	uncertain significance	13	33106862	33106862	Human		name
401878565	CV2754693	single nucleotide variant	NM_178006.4(STARD13):c.3017C>A (p.Pro1006His)	not specified [RCV004339362]	uncertain significance	13	33109903	33109903	Human		name
405722640	CV3323761	single nucleotide variant	NM_178006.4(STARD13):c.3019C>T (p.His1007Tyr)	not specified [RCV004463363]	uncertain significance	13	33109901	33109901	Human		name
597682688	CV3618390	single nucleotide variant	NM_178006.4(STARD13):c.3322G>A (p.Gly1108Ser)	not specified [RCV004857672]	uncertain significance	13	33105613	33105613	Human		name
597746749	CV3618393	single nucleotide variant	NM_178006.4(STARD13):c.3160T>C (p.Tyr1054His)	not specified [RCV004865935]	uncertain significance	13	33106822	33106822	Human		name
15147281	CV713910	single nucleotide variant	NM_178006.4(STARD13):c.3022C>T (p.Pro1008Ser)	not provided [RCV000967310]	likely benign	13	33109898	33109898	Human		name
15105720	CV753817	single nucleotide variant	NM_178006.4(STARD13):c.3143T>A (p.Val1048Glu)	not provided [RCV000915605]	likely benign	13	33106839	33106839	Human		name

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