Rell1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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28 records found for search term Rell1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597765113	CV3593216	single nucleotide variant	NM_001085400.2(RELL1):c.23G>A (p.Gly8Glu)	not specified [RCV004849950]	uncertain significance	4	37686265	37686265	Human		name
405683447	CV3315698	single nucleotide variant	NM_001085400.2(RELL1):c.61G>C (p.Ala21Pro)	not specified [RCV004443855]	uncertain significance	4	37686227	37686227	Human		name
15113636	CV709344	single nucleotide variant	NM_001085400.2(RELL1):c.432T>C (p.Tyr144=)	not provided [RCV000961528]	benign	4	37638458	37638458	Human		name
15159106	CV720960	single nucleotide variant	NM_001085400.2(RELL1):c.49T>C (p.Phe17Leu)	not provided [RCV000881133]	benign	4	37686239	37686239	Human		name
401729821	CV2683808	single nucleotide variant	NM_001085400.2(RELL1):c.113A>G (p.His38Arg)	not specified [RCV004284537]	uncertain significance	4	37649476	37649476	Human		name
401731362	CV2701329	single nucleotide variant	NM_001085400.2(RELL1):c.137C>T (p.Ser46Leu)	not specified [RCV004311704]	uncertain significance	4	37649452	37649452	Human		name
401764732	CV2705257	single nucleotide variant	NM_001085400.2(RELL1):c.212G>A (p.Gly71Asp)	not specified [RCV004311954]	uncertain significance	4	37649377	37649377	Human		name
405683432	CV3315695	single nucleotide variant	NM_001085400.2(RELL1):c.131C>A (p.Thr44Asn)	not specified [RCV004443852]	uncertain significance	4	37649458	37649458	Human		name
405683437	CV3315696	single nucleotide variant	NM_001085400.2(RELL1):c.223G>A (p.Val75Ile)	not specified [RCV004443853]	uncertain significance	4	37649366	37649366	Human		name
156034029	CV2211683	single nucleotide variant	NM_001085400.2(RELL1):c.407C>T (p.Ala136Val)	not specified [RCV004084569]	uncertain significance	4	37638483	37638483	Human		name
156074145	CV2248155	single nucleotide variant	NM_001085400.2(RELL1):c.499C>A (p.Pro167Thr)	not specified [RCV004117551]	uncertain significance	4	37635068	37635068	Human		name
156051869	CV2269387	single nucleotide variant	NM_001085400.2(RELL1):c.571G>A (p.Val191Met)	not specified [RCV004124518]	uncertain significance	4	37634996	37634996	Human		name
156030296	CV2278706	single nucleotide variant	NM_001085400.2(RELL1):c.811G>A (p.Glu271Lys)	not specified [RCV004134900]	uncertain significance	4	37631393	37631393	Human		name
156060804	CV2305437	single nucleotide variant	NM_001085400.2(RELL1):c.512C>T (p.Pro171Leu)	not specified [RCV004165161]	uncertain significance	4	37635055	37635055	Human		name
156261090	CV2322348	single nucleotide variant	NM_001085400.2(RELL1):c.572T>A (p.Val191Glu)	not specified [RCV004176102]	uncertain significance	4	37634995	37634995	Human		name
156100972	CV2367590	single nucleotide variant	NM_001085400.2(RELL1):c.580C>T (p.Arg194Trp)	not specified [RCV004211518]	uncertain significance	4	37634987	37634987	Human		name
156161182	CV2371385	single nucleotide variant	NM_001085400.2(RELL1):c.566G>C (p.Arg189Thr)	not specified [RCV004223384]	uncertain significance	4	37635001	37635001	Human		name
401744275	CV2680931	single nucleotide variant	NM_001085400.2(RELL1):c.523G>A (p.Val175Ile)	not specified [RCV004296003]	likely benign	4	37635044	37635044	Human		name
401774482	CV2713494	single nucleotide variant	NM_001085400.2(RELL1):c.433G>T (p.Asp145Tyr)	not specified [RCV004319098]	uncertain significance	4	37638457	37638457	Human		name
405683441	CV3315697	single nucleotide variant	NM_001085400.2(RELL1):c.310A>T (p.Ile104Leu)	not specified [RCV004443854]	uncertain significance	4	37649279	37649279	Human		name
405683451	CV3315699	single nucleotide variant	NM_001085400.2(RELL1):c.646C>T (p.Arg216Cys)	not specified [RCV004443856]	uncertain significance	4	37634921	37634921	Human		name
405683455	CV3315700	single nucleotide variant	NM_001085400.2(RELL1):c.647G>A (p.Arg216His)	not specified [RCV004443857]	uncertain significance	4	37634920	37634920	Human		name
405683459	CV3315701	single nucleotide variant	NM_001085400.2(RELL1):c.802A>G (p.Ser268Gly)	not specified [RCV004443858]	uncertain significance	4	37631402	37631402	Human		name
597730792	CV3593213	single nucleotide variant	NM_001085400.2(RELL1):c.473C>T (p.Pro158Leu)	not specified [RCV004863066]	uncertain significance	4	37635094	37635094	Human		name
597730804	CV3593214	single nucleotide variant	NM_001085400.2(RELL1):c.725G>A (p.Arg242Gln)	not specified [RCV004863067]	uncertain significance	4	37631479	37631479	Human		name
597730814	CV3593215	single nucleotide variant	NM_001085400.2(RELL1):c.724C>T (p.Arg242Trp)	not specified [RCV004863068]	uncertain significance	4	37631480	37631480	Human		name
597765121	CV3593218	single nucleotide variant	NM_001085400.2(RELL1):c.358A>G (p.Ile120Val)	not specified [RCV004849952]	uncertain significance	4	37647395	37647395	Human		name
598204336	CV3909316	single nucleotide variant	NM_001085400.2(RELL1):c.595C>T (p.Arg199Trp)	not specified [RCV005269524]	uncertain significance	4	37634972	37634972	Human		name

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