Setdb2 Variant Search Result - Rat Genome Database

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42 records found for search term Setdb2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582865	CV117421	single nucleotide variant	NM_001160308.1(SETDB2):c.16+237C>G	Lung cancer [RCV000097942]	uncertain significance	13	49452146	49452146	Human		name
15192114	CV778083	single nucleotide variant	NM_001160308.3(SETDB2):c.2006+6A>C	not provided [RCV000954973]	benign	13	49490916	49490916	Human		name
15160655	CV702715	single nucleotide variant	NM_001160308.3(SETDB2):c.261C>T (p.Pro87=)	not provided [RCV000947527]	benign	13	49467916	49467916	Human		name
401929802	CV2813902	single nucleotide variant	NM_001160308.3(SETDB2):c.372A>C (p.Ser124=)	not provided [RCV003390373]	likely benign	13	49476542	49476542	Human		name
597671478	CV3595409	single nucleotide variant	NM_001160308.3(SETDB2):c.89A>G (p.Asn30Ser)	not specified [RCV004856413]	uncertain significance	13	49460179	49460179	Human		name
597671514	CV3595414	single nucleotide variant	NM_001160308.3(SETDB2):c.37A>T (p.Met13Leu)	not specified [RCV004856417]	uncertain significance	13	49460127	49460127	Human		name
156232687	CV2199760	single nucleotide variant	NM_001160308.3(SETDB2):c.184A>T (p.Ile62Phe)	not specified [RCV004072482]	uncertain significance	13	49461138	49461138	Human		name
405762681	CV3321299	single nucleotide variant	NM_001160308.3(SETDB2):c.260C>T (p.Pro87Leu)	not specified [RCV004455591]	uncertain significance	13	49467915	49467915	Human		name
156175886	CV2205283	single nucleotide variant	NM_001160308.3(SETDB2):c.970A>G (p.Arg324Gly)	not specified [RCV004079903]	uncertain significance	13	49480319	49480319	Human		name
156017786	CV2222982	single nucleotide variant	NM_001160308.3(SETDB2):c.454C>A (p.Pro152Thr)	not specified [RCV004103574]	uncertain significance	13	49476624	49476624	Human		name
155985433	CV2368108	single nucleotide variant	NM_001160308.3(SETDB2):c.568G>A (p.Val190Met)	not specified [RCV004216457]	likely benign	13	49476738	49476738	Human		name
329351764	CV2455274	single nucleotide variant	NM_001160308.3(SETDB2):c.694G>T (p.Val232Leu)	not specified [RCV004274787]	uncertain significance	13	49476864	49476864	Human		name
401781286	CV2681953	single nucleotide variant	NM_001160308.3(SETDB2):c.608A>G (p.Asn203Ser)	not specified [RCV004296938]	uncertain significance	13	49476778	49476778	Human		name
401759787	CV2707148	single nucleotide variant	NM_001160308.3(SETDB2):c.332C>T (p.Ser111Phe)	not specified [RCV004315512]	uncertain significance	13	49476502	49476502	Human		name
401776872	CV2711462	single nucleotide variant	NM_001160308.3(SETDB2):c.717A>T (p.Glu239Asp)	not specified [RCV004306785]	uncertain significance	13	49476887	49476887	Human		name
405762688	CV3321300	single nucleotide variant	NM_001160308.3(SETDB2):c.831T>G (p.Phe277Leu)	not specified [RCV004455592]	uncertain significance	13	49477001	49477001	Human		name
597671463	CV3595407	single nucleotide variant	NM_001160308.3(SETDB2):c.353A>T (p.Asp118Val)	not specified [RCV004856411]	uncertain significance	13	49476523	49476523	Human		name
597671495	CV3595412	single nucleotide variant	NM_001160308.3(SETDB2):c.664T>C (p.Tyr222His)	not specified [RCV004856415]	uncertain significance	13	49476834	49476834	Human		name
597671505	CV3595413	single nucleotide variant	NM_001160308.3(SETDB2):c.724C>G (p.Pro242Ala)	not specified [RCV004856416]	uncertain significance	13	49476894	49476894	Human		name
598197541	CV3900693	single nucleotide variant	NM_001160308.3(SETDB2):c.650A>G (p.Gln217Arg)	not specified [RCV005268129]	uncertain significance	13	49476820	49476820	Human		name
156232700	CV2199761	single nucleotide variant	NM_001160308.3(SETDB2):c.1975A>G (p.Asn659Asp)	not specified [RCV004072483]	uncertain significance	13	49490879	49490879	Human		name
156219121	CV2254015	single nucleotide variant	NM_001160308.3(SETDB2):c.1359T>G (p.Ser453Arg)	not specified [RCV004129471]	uncertain significance	13	49482939	49482939	Human		name
156361673	CV2269288	single nucleotide variant	NM_001160308.3(SETDB2):c.1007T>C (p.Leu336Ser)	not specified [RCV004130435]	uncertain significance	13	49480967	49480967	Human		name
155945142	CV2291987	single nucleotide variant	NM_001160308.3(SETDB2):c.1501T>A (p.Ser501Thr)	not specified [RCV004158491]	uncertain significance	13	49485648	49485648	Human		name
156209583	CV2304524	single nucleotide variant	NM_001160308.3(SETDB2):c.1502C>G (p.Ser501Cys)	not specified [RCV004164604]	uncertain significance	13	49485649	49485649	Human		name
401720689	CV2673432	single nucleotide variant	NM_001160308.3(SETDB2):c.1564A>G (p.Lys522Glu)	not specified [RCV004288406]	uncertain significance	13	49485711	49485711	Human		name
401890346	CV2768114	single nucleotide variant	NM_001160308.3(SETDB2):c.1828A>G (p.Thr610Ala)	not specified [RCV004348343]	uncertain significance	13	49488541	49488541	Human		name
405762663	CV3321296	single nucleotide variant	NM_001160308.3(SETDB2):c.1052A>G (p.His351Arg)	not specified [RCV004455588]	uncertain significance	13	49481012	49481012	Human		name
405762672	CV3321297	single nucleotide variant	NM_001160308.3(SETDB2):c.1474A>G (p.Lys492Glu)	not specified [RCV004455589]	uncertain significance	13	49483555	49483555	Human		name
407486354	CV3483918	single nucleotide variant	NM_001160308.3(SETDB2):c.2105G>A (p.Cys702Tyr)	not specified [RCV004666111]	uncertain significance	13	49491830	49491830	Human		name
407486361	CV3483919	single nucleotide variant	NM_001160308.3(SETDB2):c.1592A>G (p.Asn531Ser)	not specified [RCV004666112]	uncertain significance	13	49488305	49488305	Human		name
407486367	CV3483920	single nucleotide variant	NM_001160308.3(SETDB2):c.1341A>T (p.Lys447Asn)	not specified [RCV004666113]	uncertain significance	13	49482921	49482921	Human		name
407486458	CV3483921	single nucleotide variant	NM_001160308.3(SETDB2):c.1973G>C (p.Arg658Thr)	not specified [RCV004667176]	uncertain significance	13	49490877	49490877	Human		name
597671454	CV3595406	single nucleotide variant	NM_001160308.3(SETDB2):c.1796G>A (p.Cys599Tyr)	not specified [RCV004856410]	uncertain significance	13	49488509	49488509	Human		name
597671470	CV3595408	single nucleotide variant	NM_001160308.3(SETDB2):c.1286T>C (p.Val429Ala)	not specified [RCV004856412]	uncertain significance	13	49482866	49482866	Human		name
597671487	CV3595411	single nucleotide variant	NM_001160308.3(SETDB2):c.1562C>T (p.Thr521Ile)	not specified [RCV004856414]	uncertain significance	13	49485709	49485709	Human		name
598197517	CV3900690	single nucleotide variant	NM_001160308.3(SETDB2):c.1109G>A (p.Arg370His)	not specified [RCV005268126]	uncertain significance	13	49481069	49481069	Human		name
598197527	CV3900691	single nucleotide variant	NM_001160308.3(SETDB2):c.1309G>A (p.Glu437Lys)	not specified [RCV005268127]	uncertain significance	13	49482889	49482889	Human		name
598197548	CV3900694	single nucleotide variant	NM_001160308.3(SETDB2):c.1865A>G (p.Asn622Ser)	not specified [RCV005268130]	uncertain significance	13	49488578	49488578	Human		name
598197555	CV3900695	single nucleotide variant	NM_001160308.3(SETDB2):c.1831T>C (p.Ser611Pro)	not specified [RCV005268131]	uncertain significance	13	49488544	49488544	Human		name
15152025	CV713950	single nucleotide variant	NM_001160308.3(SETDB2):c.1187A>T (p.Lys396Ile)	not provided [RCV000968266]	benign	13	49482767	49482767	Human		name
15179584	CV713951	single nucleotide variant	NM_001160308.3(SETDB2):c.1210G>A (p.Gly404Arg)	not provided [RCV000973945]	benign	13	49482790	49482790	Human		name

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