Itgad Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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124 records found for search term Itgad

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598171057	CV3972692	single nucleotide variant	NM_005353.3(ITGAD):c.26T>C (p.Leu9Pro)	not specified [RCV005370496]	uncertain significance	16	31393386	31393386	Human		name
405805731	CV3267990	single nucleotide variant	NM_005353.3(ITGAD):c.77C>T (p.Thr26Met)	not specified [RCV004405695]	uncertain significance	16	31394281	31394281	Human		name
8635784	CV91007	single nucleotide variant	NM_005353.2(ITGAD):c.88G>A (p.Glu30Lys)	Malignant melanoma [RCV000071105]	not provided	16	31394292	31394292	Human		name
155968983	CV2309018	single nucleotide variant	NM_005353.3(ITGAD):c.114C>A (p.Ser38Arg)	not specified [RCV004171390]	uncertain significance	16	31394318	31394318	Human		name
329385665	CV2432126	single nucleotide variant	NM_005353.3(ITGAD):c.127G>A (p.Gly43Ser)	not specified [RCV004249273]	uncertain significance	16	31394331	31394331	Human		name
401781564	CV2726563	single nucleotide variant	NM_005353.3(ITGAD):c.154C>A (p.Pro52Thr)	not specified [RCV004328738]	uncertain significance	16	31397375	31397375	Human		name
401769558	CV2731411	single nucleotide variant	NM_005353.3(ITGAD):c.182C>T (p.Thr61Met)	not specified [RCV004330774]	uncertain significance	16	31397403	31397403	Human		name
401896546	CV2780926	single nucleotide variant	NM_005353.3(ITGAD):c.151G>A (p.Ala51Thr)	not specified [RCV004354467]	uncertain significance	16	31397372	31397372	Human		name
401911648	CV2807893	single nucleotide variant	NM_005353.3(ITGAD):c.2925C>T (p.Asn975=)	not provided [RCV003426683]	likely benign	16	31423417	31423417	Human		name
405805705	CV3267976	single nucleotide variant	NM_005353.3(ITGAD):c.188G>A (p.Arg63Gln)	not specified [RCV004405681]	uncertain significance	16	31397409	31397409	Human		name
407458740	CV3451629	single nucleotide variant	NM_005353.3(ITGAD):c.296A>G (p.Asn99Ser)	not specified [RCV004633394]	uncertain significance	16	31397650	31397650	Human		name
407458755	CV3451634	single nucleotide variant	NM_005353.3(ITGAD):c.233C>T (p.Pro78Leu)	not specified [RCV004633399]	uncertain significance	16	31397454	31397454	Human		name
597793452	CV3686879	single nucleotide variant	NM_005353.3(ITGAD):c.286G>A (p.Ala96Thr)	not specified [RCV004934184]	uncertain significance	16	31397640	31397640	Human		name
597793457	CV3686880	single nucleotide variant	NM_005353.3(ITGAD):c.133T>C (p.Ser45Pro)	not specified [RCV004934185]	uncertain significance	16	31394337	31394337	Human		name
8635785	CV91008	single nucleotide variant	NM_005353.2(ITGAD):c.1095C>T (p.Phe365=)	Malignant melanoma [RCV000071106]	not provided	16	31410406	31410406	Human		name
155918209	CV2195794	single nucleotide variant	NM_005353.3(ITGAD):c.737G>A (p.Arg246Gln)	not specified [RCV004076144]	uncertain significance	16	31407547	31407547	Human		name
155985859	CV2247910	single nucleotide variant	NM_005353.3(ITGAD):c.386C>T (p.Ser129Leu)	not specified [RCV004121351]	uncertain significance	16	31397868	31397868	Human		name
156053973	CV2269546	single nucleotide variant	NM_005353.3(ITGAD):c.449A>C (p.Asp150Ala)	not specified [RCV004124650]	uncertain significance	16	31402136	31402136	Human		name
156066029	CV2270749	single nucleotide variant	NM_005353.3(ITGAD):c.644T>C (p.Val215Ala)	not specified [RCV004131809]	uncertain significance	16	31403585	31403585	Human		name
156006982	CV2357836	single nucleotide variant	NM_005353.3(ITGAD):c.923C>T (p.Pro308Leu)	not specified [RCV004205120]	uncertain significance	16	31407830	31407830	Human		name
156001735	CV2378847	single nucleotide variant	NM_005353.3(ITGAD):c.529A>G (p.Met177Val)	not specified [RCV004231289]	uncertain significance	16	31402216	31402216	Human		name
156112192	CV2387892	single nucleotide variant	NM_005353.3(ITGAD):c.761T>C (p.Ile254Thr)	not specified [RCV004236443]	uncertain significance	16	31407571	31407571	Human		name
156108074	CV2390202	single nucleotide variant	NM_005353.3(ITGAD):c.418G>A (p.Ala140Thr)	not specified [RCV004240584]	uncertain significance	16	31397900	31397900	Human		name
329400343	CV2441543	single nucleotide variant	NM_005353.3(ITGAD):c.363G>C (p.Lys121Asn)	not specified [RCV004257328]	uncertain significance	16	31397845	31397845	Human		name
329393917	CV2449956	single nucleotide variant	NM_005353.3(ITGAD):c.305G>A (p.Arg102Gln)	not specified [RCV004269023]	uncertain significance	16	31397659	31397659	Human		name
401768381	CV2735285	single nucleotide variant	NM_005353.3(ITGAD):c.934G>A (p.Val312Met)	not specified [RCV004333954]	uncertain significance	16	31407841	31407841	Human		name
405805725	CV3267987	single nucleotide variant	NM_005353.3(ITGAD):c.370T>G (p.Cys124Gly)	not specified [RCV004405692]	uncertain significance	16	31397852	31397852	Human		name
405805727	CV3267988	single nucleotide variant	NM_005353.3(ITGAD):c.424C>T (p.Pro142Ser)	not specified [RCV004405693]	uncertain significance	16	31397906	31397906	Human		name
405805729	CV3267989	single nucleotide variant	NM_005353.3(ITGAD):c.686C>T (p.Thr229Met)	not specified [RCV004405694]	uncertain significance	16	31403627	31403627	Human		name
405805733	CV3267991	single nucleotide variant	NM_005353.3(ITGAD):c.913T>C (p.Ser305Pro)	not specified [RCV004405696]	uncertain significance	16	31407820	31407820	Human		name
405805735	CV3267992	single nucleotide variant	NM_005353.3(ITGAD):c.992A>G (p.Lys331Arg)	not specified [RCV004405697]	uncertain significance	16	31407899	31407899	Human		name
597793420	CV3686869	single nucleotide variant	NM_005353.3(ITGAD):c.908T>C (p.Ile303Thr)	not specified [RCV004934174]	uncertain significance	16	31407815	31407815	Human		name
597793436	CV3686874	single nucleotide variant	NM_005353.3(ITGAD):c.674C>T (p.Thr225Met)	not specified [RCV004934179]	uncertain significance	16	31403615	31403615	Human		name
598195737	CV3972691	single nucleotide variant	NM_005353.3(ITGAD):c.722A>G (p.His241Arg)	not specified [RCV005355052]	uncertain significance	16	31407532	31407532	Human		name
598211299	CV3972693	single nucleotide variant	NM_005353.3(ITGAD):c.388C>T (p.Arg130Cys)	not specified [RCV005358659]	uncertain significance	16	31397870	31397870	Human		name
9686948	CV171572	single nucleotide variant	NM_005353.3(ITGAD):c.2836A>C (p.Lys946Gln)	Prostate cancer [RCV000149167]	uncertain significance	16	31423169	31423169	Human	2	name
156183690	CV2198530	single nucleotide variant	NM_005353.3(ITGAD):c.1267G>C (p.Ala423Pro)	not specified [RCV004075557]	uncertain significance	16	31410789	31410789	Human		name
156166267	CV2200901	single nucleotide variant	NM_005353.3(ITGAD):c.1951G>A (p.Ala651Thr)	not specified [RCV004081519]	uncertain significance	16	31413201	31413201	Human		name
155981657	CV2208475	single nucleotide variant	NM_005353.3(ITGAD):c.2375T>C (p.Val792Ala)	not specified [RCV004091012]	uncertain significance	16	31416522	31416522	Human		name
155972730	CV2214362	single nucleotide variant	NM_005353.3(ITGAD):c.1119C>A (p.Ser373Arg)	not specified [RCV004088137]	uncertain significance	16	31410430	31410430	Human		name
156381677	CV2215139	single nucleotide variant	NM_005353.3(ITGAD):c.2635T>C (p.Phe879Leu)	not specified [RCV004086860]	uncertain significance	16	31418319	31418319	Human		name
156330899	CV2224335	single nucleotide variant	NM_005353.3(ITGAD):c.2749G>T (p.Val917Leu)	not specified [RCV004097683]	uncertain significance	16	31418533	31418533	Human		name
155952385	CV2238950	single nucleotide variant	NM_005353.3(ITGAD):c.1229T>C (p.Leu410Pro)	not specified [RCV004109847]	uncertain significance	16	31410751	31410751	Human		name
156231993	CV2245125	single nucleotide variant	NM_005353.3(ITGAD):c.1171A>C (p.Asn391His)	not specified [RCV004106919]	uncertain significance	16	31410482	31410482	Human		name
156100054	CV2306589	single nucleotide variant	NM_005353.3(ITGAD):c.2474C>T (p.Ser825Leu)	not specified [RCV004157193]	uncertain significance	16	31416621	31416621	Human		name
156247734	CV2307013	single nucleotide variant	NM_005353.3(ITGAD):c.2845G>A (p.Glu949Lys)	not specified [RCV004159518]	uncertain significance	16	31423178	31423178	Human		name
156290260	CV2309805	single nucleotide variant	NM_005353.3(ITGAD):c.2792C>A (p.Ser931Tyr)	not specified [RCV004160924]	uncertain significance	16	31423125	31423125	Human		name
155960966	CV2314086	single nucleotide variant	NM_005353.3(ITGAD):c.1254C>G (p.Asn418Lys)	not specified [RCV004164358]	uncertain significance	16	31410776	31410776	Human		name
156162478	CV2323536	single nucleotide variant	NM_005353.3(ITGAD):c.2770A>G (p.Met924Val)	not specified [RCV004165737]	likely benign	16	31418554	31418554	Human		name
156285910	CV2327186	single nucleotide variant	NM_005353.3(ITGAD):c.2474C>G (p.Ser825Trp)	not specified [RCV004174653]	uncertain significance	16	31416621	31416621	Human		name
156200598	CV2338229	single nucleotide variant	NM_005353.3(ITGAD):c.1673C>T (p.Ala558Val)	not specified [RCV004599553]	uncertain significance	16	31411483	31411483	Human		name
156182832	CV2338230	single nucleotide variant	NM_005353.3(ITGAD):c.1676C>T (p.Ser559Leu)	not specified [RCV004599554]	uncertain significance	16	31411486	31411486	Human		name
156182850	CV2338231	single nucleotide variant	NM_005353.3(ITGAD):c.1679A>G (p.Glu560Gly)	not specified [RCV004186294]	likely benign	16	31411489	31411489	Human		name
156182868	CV2338232	single nucleotide variant	NM_005353.3(ITGAD):c.1681T>C (p.Ser561Pro)	not specified [RCV004599555]	uncertain significance	16	31411491	31411491	Human		name
156200617	CV2338234	single nucleotide variant	NM_005353.3(ITGAD):c.1684G>A (p.Gly562Ser)	not specified [RCV004186295]	likely benign	16	31411494	31411494	Human		name
156337466	CV2343055	single nucleotide variant	NM_005353.3(ITGAD):c.2687G>T (p.Ser896Ile)	not specified [RCV004192652]	uncertain significance	16	31418371	31418371	Human		name
155936614	CV2375951	single nucleotide variant	NM_005353.3(ITGAD):c.1273C>T (p.Arg425Cys)	not specified [RCV004218159]	uncertain significance	16	31410795	31410795	Human		name
156344711	CV2381892	single nucleotide variant	NM_005353.3(ITGAD):c.1189G>A (p.Val397Met)	not specified [RCV004225833]	uncertain significance	16	31410500	31410500	Human		name
156001481	CV2391914	single nucleotide variant	NM_005353.3(ITGAD):c.1359C>G (p.Ile453Met)	not specified [RCV004235781]	uncertain significance	16	31411078	31411078	Human		name
156145295	CV2393776	single nucleotide variant	NM_005353.3(ITGAD):c.1494G>T (p.Arg498Ser)	not specified [RCV004233611]	uncertain significance	16	31411213	31411213	Human		name
156223968	CV2395059	single nucleotide variant	NM_005353.3(ITGAD):c.1075C>T (p.Leu359Phe)	not specified [RCV004236745]	uncertain significance	16	31408490	31408490	Human		name
156247925	CV2396952	single nucleotide variant	NM_005353.3(ITGAD):c.2239C>T (p.Arg747Cys)	not specified [RCV004234064]	uncertain significance	16	31414947	31414947	Human		name
329357318	CV2431336	single nucleotide variant	NM_005353.3(ITGAD):c.1073C>A (p.Ala358Asp)	not specified [RCV004252456]	uncertain significance	16	31408488	31408488	Human		name
329384885	CV2435222	single nucleotide variant	NM_005353.3(ITGAD):c.2959C>T (p.Pro987Ser)	not specified [RCV004252859]	uncertain significance	16	31423451	31423451	Human		name
329376513	CV2438260	single nucleotide variant	NM_005353.3(ITGAD):c.2254G>A (p.Val752Met)	not specified [RCV004257021]	likely benign	16	31414962	31414962	Human		name
329392666	CV2439104	single nucleotide variant	NM_005353.3(ITGAD):c.1957G>A (p.Val653Ile)	not specified [RCV004266392]	likely benign	16	31413207	31413207	Human		name
329399456	CV2447084	single nucleotide variant	NM_005353.3(ITGAD):c.1417G>A (p.Asp473Asn)	not specified [RCV004259958]	uncertain significance	16	31411136	31411136	Human		name
329388898	CV2448477	single nucleotide variant	NM_005353.3(ITGAD):c.1628C>T (p.Pro543Leu)	not specified [RCV004259168]	uncertain significance	16	31411438	31411438	Human		name
329371833	CV2454911	single nucleotide variant	NM_005353.3(ITGAD):c.1289G>T (p.Gly430Val)	not specified [RCV004270404]	uncertain significance	16	31410811	31410811	Human		name
329387711	CV2470916	single nucleotide variant	NM_005353.3(ITGAD):c.1646G>A (p.Arg549Gln)	not specified [RCV004276110]	likely benign	16	31411456	31411456	Human		name
401780364	CV2673991	single nucleotide variant	NM_005353.3(ITGAD):c.1979G>T (p.Ser660Ile)	not specified [RCV004293359]	uncertain significance	16	31413229	31413229	Human		name
401732933	CV2691153	single nucleotide variant	NM_005353.3(ITGAD):c.1813G>A (p.Ala605Thr)	not specified [RCV004302934]	uncertain significance	16	31412943	31412943	Human		name
401737505	CV2695819	single nucleotide variant	NM_005353.3(ITGAD):c.1099G>A (p.Gly367Arg)	not specified [RCV004308103]	uncertain significance	16	31410410	31410410	Human		name
401752376	CV2723213	single nucleotide variant	NM_005353.3(ITGAD):c.2833A>G (p.Met945Val)	not specified [RCV004329449]	uncertain significance	16	31423166	31423166	Human		name
401890118	CV2763508	single nucleotide variant	NM_005353.3(ITGAD):c.2576G>A (p.Arg859His)	not specified [RCV004343035]	uncertain significance	16	31418151	31418151	Human		name
401856526	CV2764843	single nucleotide variant	NM_005353.3(ITGAD):c.2971C>T (p.Leu991Phe)	not specified [RCV004334940]	uncertain significance	16	31423574	31423574	Human		name
401873386	CV2776564	single nucleotide variant	NM_005353.3(ITGAD):c.2275A>T (p.Thr759Ser)	not specified [RCV004355659]	uncertain significance	16	31414983	31414983	Human		name
405805693	CV3267969	single nucleotide variant	NM_005353.3(ITGAD):c.1436C>A (p.Ala479Asp)	not specified [RCV004405674]	uncertain significance	16	31411155	31411155	Human		name
405805698	CV3267972	single nucleotide variant	NM_005353.3(ITGAD):c.1528C>T (p.Arg510Cys)	not specified [RCV004405677]	likely benign	16	31411338	31411338	Human		name
405805699	CV3267973	single nucleotide variant	NM_005353.3(ITGAD):c.1534G>A (p.Glu512Lys)	not specified [RCV004405678]	uncertain significance	16	31411344	31411344	Human		name
405805701	CV3267974	single nucleotide variant	NM_005353.3(ITGAD):c.1619T>C (p.Ile540Thr)	not specified [RCV004405679]	uncertain significance	16	31411429	31411429	Human		name
405805703	CV3267975	single nucleotide variant	NM_005353.3(ITGAD):c.1816C>T (p.Arg606Trp)	not specified [RCV004405680]	uncertain significance	16	31412946	31412946	Human		name
405805707	CV3267977	single nucleotide variant	NM_005353.3(ITGAD):c.2033T>C (p.Leu678Pro)	not specified [RCV004405682]	uncertain significance	16	31414487	31414487	Human		name
405805709	CV3267978	single nucleotide variant	NM_005353.3(ITGAD):c.2516G>T (p.Ser839Ile)	not specified [RCV004405683]	uncertain significance	16	31418091	31418091	Human		name
405805710	CV3267979	single nucleotide variant	NM_005353.3(ITGAD):c.2525G>A (p.Arg842His)	not specified [RCV004405684]	likely benign	16	31418100	31418100	Human		name
405805712	CV3267980	single nucleotide variant	NM_005353.3(ITGAD):c.2753A>C (p.Lys918Thr)	not specified [RCV004405685]	uncertain significance	16	31418537	31418537	Human		name
405805714	CV3267981	single nucleotide variant	NM_005353.3(ITGAD):c.2791T>A (p.Ser931Thr)	not specified [RCV004405686]	uncertain significance	16	31423124	31423124	Human		name
405805716	CV3267982	single nucleotide variant	NM_005353.3(ITGAD):c.2852G>A (p.Arg951Gln)	not specified [RCV004405687]	uncertain significance	16	31423185	31423185	Human		name
405805870	CV3267983	single nucleotide variant	NM_005353.3(ITGAD):c.2858G>A (p.Arg953His)	not specified [RCV004405688]	uncertain significance	16	31423191	31423191	Human		name
407458752	CV3451633	single nucleotide variant	NM_005353.3(ITGAD):c.1243G>C (p.Gly415Arg)	not specified [RCV004633398]	uncertain significance	16	31410765	31410765	Human		name
407458758	CV3451635	single nucleotide variant	NM_005353.3(ITGAD):c.2868C>A (p.Asn956Lys)	not specified [RCV004633400]	uncertain significance	16	31423360	31423360	Human		name
407458763	CV3451638	single nucleotide variant	NM_005353.3(ITGAD):c.1242G>C (p.Lys414Asn)	not specified [RCV004633402]	uncertain significance	16	31410764	31410764	Human		name
407458766	CV3451639	single nucleotide variant	NM_005353.3(ITGAD):c.2533T>C (p.Cys845Arg)	not specified [RCV004633403]	uncertain significance	16	31418108	31418108	Human		name
407458769	CV3451640	single nucleotide variant	NM_005353.3(ITGAD):c.2447T>C (p.Val816Ala)	not specified [RCV004633404]	uncertain significance	16	31416594	31416594	Human		name
407458772	CV3451641	single nucleotide variant	NM_005353.3(ITGAD):c.2951T>C (p.Met984Thr)	not specified [RCV004633405]	uncertain significance	16	31423443	31423443	Human		name
597793409	CV3686866	single nucleotide variant	NM_005353.3(ITGAD):c.2557G>A (p.Glu853Lys)	not specified [RCV004934171]	uncertain significance	16	31418132	31418132	Human		name
597793413	CV3686867	single nucleotide variant	NM_005353.3(ITGAD):c.2435A>G (p.Tyr812Cys)	not specified [RCV004934172]	uncertain significance	16	31416582	31416582	Human		name
597793423	CV3686870	single nucleotide variant	NM_005353.3(ITGAD):c.2905T>C (p.Trp969Arg)	not specified [RCV004934175]	uncertain significance	16	31423397	31423397	Human		name
597793426	CV3686871	single nucleotide variant	NM_005353.3(ITGAD):c.1162A>G (p.Thr388Ala)	not specified [RCV004934176]	uncertain significance	16	31410473	31410473	Human		name
597793429	CV3686872	single nucleotide variant	NM_005353.3(ITGAD):c.2251G>A (p.Ala751Thr)	not specified [RCV004934177]	uncertain significance	16	31414959	31414959	Human		name
597793432	CV3686873	single nucleotide variant	NM_005353.3(ITGAD):c.1477G>A (p.Val493Met)	not specified [RCV004934178]	uncertain significance	16	31411196	31411196	Human		name
597793440	CV3686875	single nucleotide variant	NM_005353.3(ITGAD):c.2926G>A (p.Gly976Arg)	not specified [RCV004934180]	uncertain significance	16	31423418	31423418	Human		name
597793443	CV3686876	single nucleotide variant	NM_005353.3(ITGAD):c.1796T>G (p.Met599Arg)	not specified [RCV004934181]	uncertain significance	16	31412926	31412926	Human		name
597793446	CV3686877	single nucleotide variant	NM_005353.3(ITGAD):c.1124C>A (p.Ser375Tyr)	not specified [RCV004934182]	uncertain significance	16	31410435	31410435	Human		name
597793449	CV3686878	single nucleotide variant	NM_005353.3(ITGAD):c.2306G>A (p.Gly769Glu)	not specified [RCV004934183]	uncertain significance	16	31416235	31416235	Human		name
597793459	CV3686881	single nucleotide variant	NM_005353.3(ITGAD):c.2561G>A (p.Gly854Asp)	not specified [RCV004934186]	uncertain significance	16	31418136	31418136	Human		name
598171061	CV3972694	single nucleotide variant	NM_005353.3(ITGAD):c.1564G>A (p.Ala522Thr)	not specified [RCV005370497]	uncertain significance	16	31411374	31411374	Human		name
598171066	CV3972695	single nucleotide variant	NM_005353.3(ITGAD):c.2009G>C (p.Ser670Thr)	not specified [RCV005370498]	uncertain significance	16	31414463	31414463	Human		name
598195747	CV3972698	single nucleotide variant	NM_005353.3(ITGAD):c.2539A>T (p.Thr847Ser)	not specified [RCV005355054]	uncertain significance	16	31418114	31418114	Human		name
598195752	CV3972699	single nucleotide variant	NM_005353.3(ITGAD):c.1197G>A (p.Met399Ile)	not specified [RCV005355055]	uncertain significance	16	31410508	31410508	Human		name
156175348	CV2278200	single nucleotide variant	NM_005353.3(ITGAD):c.3217G>A (p.Val1073Met)	not specified [RCV004141392]	uncertain significance	16	31424159	31424159	Human		name
156005710	CV2281655	single nucleotide variant	NM_005353.3(ITGAD):c.3155G>A (p.Arg1052His)	not specified [RCV004153943]	uncertain significance	16	31423954	31423954	Human		name
155918532	CV2333021	single nucleotide variant	NM_005353.3(ITGAD):c.3389G>A (p.Arg1130His)	not specified [RCV004194320]	uncertain significance	16	31426031	31426031	Human		name
329389853	CV2441373	single nucleotide variant	NM_005353.3(ITGAD):c.3373C>G (p.Leu1125Val)	not specified [RCV004257178]	uncertain significance	16	31426015	31426015	Human		name
401753236	CV2720680	single nucleotide variant	NM_005353.3(ITGAD):c.3260A>G (p.Gln1087Arg)	not specified [RCV004328041]	uncertain significance	16	31424202	31424202	Human		name
401886331	CV2771177	single nucleotide variant	NM_005353.3(ITGAD):c.3434C>T (p.Thr1145Ile)	not specified [RCV004346171]	uncertain significance	16	31426076	31426076	Human		name
405805720	CV3267984	single nucleotide variant	NM_005353.3(ITGAD):c.3104A>G (p.Gln1035Arg)	not specified [RCV004405689]	uncertain significance	16	31423903	31423903	Human		name
405805722	CV3267985	single nucleotide variant	NM_005353.3(ITGAD):c.3271G>A (p.Val1091Met)	not specified [RCV004405690]	uncertain significance	16	31424476	31424476	Human		name
405805724	CV3267986	single nucleotide variant	NM_005353.3(ITGAD):c.3458G>C (p.Cys1153Ser)	not specified [RCV004405691]	uncertain significance	16	31426100	31426100	Human		name
407458746	CV3451631	single nucleotide variant	NM_005353.3(ITGAD):c.3179T>C (p.Leu1060Ser)	not specified [RCV004633396]	likely benign	16	31424121	31424121	Human		name
407458749	CV3451632	single nucleotide variant	NM_005353.3(ITGAD):c.3076C>T (p.Arg1026Cys)	not specified [RCV004633397]	uncertain significance	16	31423875	31423875	Human		name
407458761	CV3451636	single nucleotide variant	NM_005353.3(ITGAD):c.3347C>T (p.Ala1116Val)	not specified [RCV004633401]	uncertain significance	16	31424552	31424552	Human		name
597793416	CV3686868	single nucleotide variant	NM_005353.3(ITGAD):c.3064T>G (p.Cys1022Gly)	not specified [RCV004934173]	uncertain significance	16	31423863	31423863	Human		name
598171071	CV3972696	single nucleotide variant	NM_005353.3(ITGAD):c.3056T>C (p.Ile1019Thr)	not specified [RCV005370499]	uncertain significance	16	31423855	31423855	Human		name

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