Suv39h2 Variant Search Result - Rat Genome Database

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21 records found for search term Suv39h2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15166840	CV730679	single nucleotide variant	NM_001193424.2(SUV39H2):c.850-6G>C	not provided [RCV000882720]	benign	10	14899533	14899533	Human		name
150512349	CV1245392	single nucleotide variant	NM_001193424.2(SUV39H2):c.850-305C>T	Histiocytic medullary reticulosis [RCV001661373]\|Severe combined immunodeficiency due to DCLRE1C deficiency [RCV001661372]\|not provided [RCV004718943]\|not specified [RCV003487630]	benign	10	14899234	14899234	Human	2	name
153304507	CV1686991	single nucleotide variant	NM_001193424.2(SUV39H2):c.850-352G>A	not provided [RCV002262278]	likely benign	10	14899187	14899187	Human		name
402476836	CV2849355	single nucleotide variant	NM_001193424.2(SUV39H2):c.850-483T>G	not specified [RCV003489227]	benign	10	14899056	14899056	Human		name
405275474	CV3211103	single nucleotide variant	NM_001193424.2(SUV39H2):c.850-295C>G	SUV39H2-related disorder [RCV003937098]	likely benign	10	14899244	14899244	Human		name , trait , alternate_id
329352921	CV2470656	single nucleotide variant	NM_001193424.2(SUV39H2):c.43C>A (p.Pro15Thr)	not specified [RCV004273642]	uncertain significance	10	14881511	14881511	Human		name
407504934	CV3481968	single nucleotide variant	NM_001193424.2(SUV39H2):c.61G>C (p.Asp21His)	not specified [RCV004670713]	uncertain significance	10	14881529	14881529	Human		name
597769660	CV3608801	single nucleotide variant	NM_001193424.2(SUV39H2):c.28G>A (p.Gly10Arg)	not specified [RCV004871294]	uncertain significance	10	14878916	14878916	Human		name
598222328	CV3912603	single nucleotide variant	NM_001193424.2(SUV39H2):c.121A>G (p.Lys41Glu)	not specified [RCV005293777]	uncertain significance	10	14881589	14881589	Human		name
155971215	CV2237382	single nucleotide variant	NM_001193424.2(SUV39H2):c.526A>C (p.Lys176Gln)	not specified [RCV004104570]	uncertain significance	10	14897194	14897194	Human		name
155975377	CV2327771	single nucleotide variant	NM_001193424.2(SUV39H2):c.614A>C (p.Glu205Ala)	not specified [RCV004179117]	uncertain significance	10	14897282	14897282	Human		name
156185874	CV2397509	single nucleotide variant	NM_001193424.2(SUV39H2):c.781C>T (p.Arg261Cys)	not specified [RCV004236978]	likely benign	10	14897449	14897449	Human		name
401896457	CV2781405	single nucleotide variant	NM_001193424.2(SUV39H2):c.489G>T (p.Glu163Asp)	not specified [RCV004352408]	uncertain significance	10	14897157	14897157	Human		name
401859704	CV2793018	single nucleotide variant	NM_001193424.2(SUV39H2):c.899A>G (p.Lys300Arg)	not specified [RCV004360353]	uncertain significance	10	14899588	14899588	Human		name
407450983	CV3481969	single nucleotide variant	NM_001193424.2(SUV39H2):c.719C>G (p.Pro240Arg)	not specified [RCV004670714]	uncertain significance	10	14897387	14897387	Human		name
597769665	CV3608803	single nucleotide variant	NM_001193424.2(SUV39H2):c.320G>T (p.Gly107Val)	not specified [RCV004871296]	uncertain significance	10	14896988	14896988	Human		name
597769670	CV3608804	single nucleotide variant	NM_001193424.2(SUV39H2):c.463T>C (p.Phe155Leu)	not specified [RCV004871297]	uncertain significance	10	14897131	14897131	Human		name
598263628	CV3912602	single nucleotide variant	NM_001193424.2(SUV39H2):c.356T>C (p.Leu119Ser)	not specified [RCV005280564]	uncertain significance	10	14897024	14897024	Human		name
405707365	CV3327665	single nucleotide variant	NM_001193424.2(SUV39H2):c.1159C>G (p.His387Asp)	not specified [RCV004461257]	uncertain significance	10	14902438	14902438	Human		name
407450986	CV3481970	single nucleotide variant	NM_001193424.2(SUV39H2):c.1139T>C (p.Ile380Thr)	not specified [RCV004670715]	uncertain significance	10	14902418	14902418	Human		name
597689329	CV3608802	single nucleotide variant	NM_001193424.2(SUV39H2):c.1022A>T (p.Asn341Ile)	not specified [RCV004871295]	uncertain significance	10	14901158	14901158	Human		name

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