Zbtb7c Variant Search Result - Rat Genome Database

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65 records found for search term Zbtb7c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15169242	CV741389	single nucleotide variant	NM_001318841.2(ZBTB7C):c.993C>T (p.Tyr331=)	not provided [RCV000905018]	benign	18	48040115	48040115	Human		name
150481815	CV1258984	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1662A>G (p.Thr554=)	not provided [RCV001686114]	benign	18	48029458	48029458	Human		name
155969362	CV2337946	single nucleotide variant	NM_001318841.2(ZBTB7C):c.220G>A (p.Val74Ile)	not specified [RCV004185995]	uncertain significance	18	48040888	48040888	Human		name
15182508	CV715992	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1743C>T (p.Asn581=)	not provided [RCV000974648]	benign\|likely benign	18	48029377	48029377	Human		name
155918399	CV2236817	single nucleotide variant	NM_001318841.2(ZBTB7C):c.481G>A (p.Glu161Lys)	not specified [RCV004112581]	uncertain significance	18	48040627	48040627	Human		name
155923405	CV2251950	single nucleotide variant	NM_001318841.2(ZBTB7C):c.539C>T (p.Pro180Leu)	not specified [RCV004119916]	uncertain significance	18	48040569	48040569	Human		name
156029270	CV2278610	single nucleotide variant	NM_001318841.2(ZBTB7C):c.994G>A (p.Gly332Ser)	not specified [RCV004133033]	uncertain significance	18	48040114	48040114	Human		name
156197612	CV2293586	single nucleotide variant	NM_001318841.2(ZBTB7C):c.364G>A (p.Val122Met)	not specified [RCV004153108]	uncertain significance	18	48040744	48040744	Human		name
155961182	CV2311878	single nucleotide variant	NM_001318841.2(ZBTB7C):c.808C>A (p.Leu270Met)	not specified [RCV004170715]	uncertain significance	18	48040300	48040300	Human		name
155969411	CV2335464	single nucleotide variant	NM_001318841.2(ZBTB7C):c.483G>T (p.Glu161Asp)	not specified [RCV004191636]	uncertain significance	18	48040625	48040625	Human		name
155994331	CV2379532	single nucleotide variant	NM_001318841.2(ZBTB7C):c.326A>G (p.Asn109Ser)	not specified [RCV004217241]	uncertain significance	18	48040782	48040782	Human		name
329377672	CV2435997	single nucleotide variant	NM_001318841.2(ZBTB7C):c.889C>G (p.Leu297Val)	not specified [RCV004255218]	uncertain significance	18	48040219	48040219	Human		name
329391226	CV2447908	single nucleotide variant	NM_001318841.2(ZBTB7C):c.980C>T (p.Ala327Val)	not specified [RCV004260720]	uncertain significance	18	48040128	48040128	Human		name
329368124	CV2457076	single nucleotide variant	NM_001318841.2(ZBTB7C):c.443A>T (p.Asp148Val)	not specified [RCV004264860]	uncertain significance	18	48040665	48040665	Human		name
401718823	CV2679319	single nucleotide variant	NM_001318841.2(ZBTB7C):c.515C>G (p.Ala172Gly)	not specified [RCV004285859]	uncertain significance	18	48040593	48040593	Human		name
401745384	CV2681254	single nucleotide variant	NM_001318841.2(ZBTB7C):c.493G>A (p.Asp165Asn)	not specified [RCV004289388]	uncertain significance	18	48040615	48040615	Human		name
401724330	CV2681384	single nucleotide variant	NM_001318841.2(ZBTB7C):c.394G>T (p.Asp132Tyr)	not specified [RCV004291929]	uncertain significance	18	48040714	48040714	Human		name
401754090	CV2715543	single nucleotide variant	NM_001318841.2(ZBTB7C):c.622C>T (p.Pro208Ser)	not specified [RCV004326943]	uncertain significance	18	48040486	48040486	Human		name
401774403	CV2727830	single nucleotide variant	NM_001318841.2(ZBTB7C):c.716C>G (p.Ala239Gly)	not specified [RCV004323852]	uncertain significance	18	48040392	48040392	Human		name
401877692	CV2761273	single nucleotide variant	NM_001318841.2(ZBTB7C):c.793G>A (p.Gly265Ser)	not specified [RCV004341144]	uncertain significance	18	48040315	48040315	Human		name
405808313	CV3353116	single nucleotide variant	NM_001318841.2(ZBTB7C):c.944C>T (p.Pro315Leu)	not specified [RCV004481142]	uncertain significance	18	48040164	48040164	Human		name
405808301	CV3357066	single nucleotide variant	NM_001318841.2(ZBTB7C):c.391G>C (p.Gly131Arg)	not specified [RCV004481136]	uncertain significance	18	48040717	48040717	Human		name
405808303	CV3357067	single nucleotide variant	NM_001318841.2(ZBTB7C):c.397G>A (p.Gly133Arg)	not specified [RCV004481137]	uncertain significance	18	48040711	48040711	Human		name
405808305	CV3357068	single nucleotide variant	NM_001318841.2(ZBTB7C):c.412G>C (p.Asp138His)	not specified [RCV004481138]	uncertain significance	18	48040696	48040696	Human		name
405808307	CV3357069	single nucleotide variant	NM_001318841.2(ZBTB7C):c.430G>A (p.Asp144Asn)	not specified [RCV004481139]	uncertain significance	18	48040678	48040678	Human		name
405808309	CV3357070	single nucleotide variant	NM_001318841.2(ZBTB7C):c.553T>A (p.Cys185Ser)	not specified [RCV004481140]	uncertain significance	18	48040555	48040555	Human		name
405808311	CV3357071	single nucleotide variant	NM_001318841.2(ZBTB7C):c.721A>G (p.Ile241Val)	not specified [RCV004481141]	uncertain significance	18	48040387	48040387	Human		name
407466312	CV3491835	single nucleotide variant	NM_001318841.2(ZBTB7C):c.925T>G (p.Phe309Val)	not specified [RCV004688994]	uncertain significance	18	48040183	48040183	Human		name
597694641	CV3624500	single nucleotide variant	NM_001318841.2(ZBTB7C):c.438A>T (p.Glu146Asp)	not specified [RCV004884966]	uncertain significance	18	48040670	48040670	Human		name
597694675	CV3624503	single nucleotide variant	NM_001318841.2(ZBTB7C):c.546C>A (p.Asp182Glu)	not specified [RCV004884969]	uncertain significance	18	48040562	48040562	Human		name
597694696	CV3624505	single nucleotide variant	NM_001318841.2(ZBTB7C):c.850A>C (p.Ile284Leu)	not specified [RCV004884971]	uncertain significance	18	48040258	48040258	Human		name
597753035	CV3624506	single nucleotide variant	NM_001318841.2(ZBTB7C):c.395A>G (p.Asp132Gly)	not specified [RCV004893071]	uncertain significance	18	48040713	48040713	Human		name
597694707	CV3624507	single nucleotide variant	NM_001318841.2(ZBTB7C):c.339G>T (p.Met113Ile)	not specified [RCV004884972]	uncertain significance	18	48040769	48040769	Human		name
597694716	CV3624508	single nucleotide variant	NM_001318841.2(ZBTB7C):c.479A>G (p.Glu160Gly)	not specified [RCV004884973]	uncertain significance	18	48040629	48040629	Human		name
597694726	CV3624509	single nucleotide variant	NM_001318841.2(ZBTB7C):c.503C>T (p.Thr168Met)	not specified [RCV004884974]	uncertain significance	18	48040605	48040605	Human		name
598243752	CV3930499	single nucleotide variant	NM_001318841.2(ZBTB7C):c.857A>C (p.Asn286Thr)	not specified [RCV005297336]	uncertain significance	18	48040251	48040251	Human		name
598196964	CV3930501	single nucleotide variant	NM_001318841.2(ZBTB7C):c.577G>T (p.Asp193Tyr)	not specified [RCV005313597]	uncertain significance	18	48040531	48040531	Human		name
156234730	CV2193330	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1792G>A (p.Gly598Ser)	not specified [RCV004072834]	uncertain significance	18	48029328	48029328	Human		name
155918193	CV2195788	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1351G>A (p.Glu451Lys)	not specified [RCV004076138]	uncertain significance	18	48029769	48029769	Human		name
156254477	CV2203229	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1681C>T (p.Arg561Cys)	not specified [RCV004071267]	uncertain significance	18	48029439	48029439	Human		name
156124016	CV2234157	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1799C>T (p.Ala600Val)	not specified [RCV004106246]	uncertain significance	18	48029321	48029321	Human		name
156361896	CV2322920	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1454C>G (p.Ala485Gly)	not specified [RCV004185368]	uncertain significance	18	48029666	48029666	Human		name
156255362	CV2325743	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1585A>G (p.Ser529Gly)	not specified [RCV004173637]	uncertain significance	18	48029535	48029535	Human		name
156280575	CV2338401	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1481G>A (p.Gly494Glu)	not specified [RCV004186448]	uncertain significance	18	48029639	48029639	Human		name
156181025	CV2353050	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1735G>A (p.Ala579Thr)	not specified [RCV004203537]	uncertain significance	18	48029385	48029385	Human		name
156142764	CV2386179	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1073T>C (p.Leu358Pro)	not specified [RCV004229223]	uncertain significance	18	48040035	48040035	Human		name
329378898	CV2443202	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1510G>A (p.Ala504Thr)	not specified [RCV004260017]	uncertain significance	18	48029610	48029610	Human		name
401743750	CV2688020	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1531C>G (p.Leu511Val)	not specified [RCV004305094]	uncertain significance	18	48029589	48029589	Human		name
401729709	CV2690467	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1333G>A (p.Val445Met)	not specified [RCV004304236]	uncertain significance	18	48029787	48029787	Human		name
401762997	CV2707422	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1160C>G (p.Thr387Ser)	not specified [RCV004312809]	uncertain significance	18	48039948	48039948	Human		name
405808287	CV3357059	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1183A>C (p.Thr395Pro)	not specified [RCV004481129]	uncertain significance	18	48039925	48039925	Human		name
405808289	CV3357060	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1192G>A (p.Glu398Lys)	not specified [RCV004481130]	uncertain significance	18	48039916	48039916	Human		name
405808291	CV3357061	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1567G>A (p.Val523Met)	not specified [RCV004481131]	uncertain significance	18	48029553	48029553	Human		name
405808293	CV3357062	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1707C>A (p.Asn569Lys)	not specified [RCV004481132]	uncertain significance	18	48029413	48029413	Human		name
405808295	CV3357063	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1708G>C (p.Ala570Pro)	not specified [RCV004481133]	uncertain significance	18	48029412	48029412	Human		name
405808297	CV3357064	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1715G>A (p.Gly572Asp)	not specified [RCV004481134]	uncertain significance	18	48029405	48029405	Human		name
405808299	CV3357065	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1790C>T (p.Ala597Val)	not specified [RCV004481135]	uncertain significance	18	48029330	48029330	Human		name
407466303	CV3491833	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1199G>A (p.Arg400His)	not specified [RCV004688992]	uncertain significance	18	48039909	48039909	Human		name
407466307	CV3491834	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1007A>G (p.Asn336Ser)	not specified [RCV004688993]	uncertain significance	18	48040101	48040101	Human		name
597694664	CV3624502	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1034G>A (p.Gly345Asp)	not specified [RCV004884968]	uncertain significance	18	48040074	48040074	Human		name
597694685	CV3624504	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1681C>A (p.Arg561Ser)	not specified [RCV004884970]	uncertain significance	18	48029439	48029439	Human		name
598196957	CV3930497	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1537G>A (p.Glu513Lys)	not specified [RCV005313596]	uncertain significance	18	48029583	48029583	Human		name
598243745	CV3930498	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1039T>C (p.Phe347Leu)	not specified [RCV005297335]	uncertain significance	18	48040069	48040069	Human		name
598243758	CV3930500	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1682G>C (p.Arg561Pro)	not specified [RCV005297337]	uncertain significance	18	48029438	48029438	Human		name
15129825	CV741388	single nucleotide variant	NM_001318841.2(ZBTB7C):c.1685C>T (p.Ala562Val)	not provided [RCV000897506]	benign	18	48029435	48029435	Human		name

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