Haus2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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22 records found for search term Haus2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597781262	CV3682172	single nucleotide variant	NM_018097.3(HAUS2):c.7G>T (p.Ala3Ser)	not specified [RCV004930850]	uncertain significance	15	42548879	42548879	Human		name
598265499	CV3971413	single nucleotide variant	NM_018097.3(HAUS2):c.26C>A (p.Pro9Gln)	not specified [RCV005349070]	uncertain significance	15	42548898	42548898	Human		name
329396336	CV2462527	single nucleotide variant	NM_018097.3(HAUS2):c.99G>C (p.Met33Ile)	not specified [RCV004278485]	uncertain significance	15	42558203	42558203	Human		name
329352697	CV2470336	single nucleotide variant	NM_018097.3(HAUS2):c.34G>A (p.Ala12Thr)	not specified [RCV004279726]	uncertain significance	15	42548906	42548906	Human		name
401887145	CV2775658	single nucleotide variant	NM_018097.3(HAUS2):c.89A>G (p.Asn30Ser)	not specified [RCV004350799]	uncertain significance	15	42548961	42548961	Human		name
155983162	CV2344278	single nucleotide variant	NM_018097.3(HAUS2):c.200T>C (p.Ile67Thr)	not specified [RCV004195044]	uncertain significance	15	42559352	42559352	Human		name
156387301	CV2372701	single nucleotide variant	NM_018097.3(HAUS2):c.248T>C (p.Phe83Ser)	not specified [RCV004221895]	likely benign	15	42559400	42559400	Human		name
401736604	CV2683063	single nucleotide variant	NM_018097.3(HAUS2):c.285G>T (p.Met95Ile)	not specified [RCV004283838]	uncertain significance	15	42561298	42561298	Human		name
405789270	CV3270016	single nucleotide variant	NM_018097.3(HAUS2):c.201T>G (p.Ile67Met)	not specified [RCV004399192]	uncertain significance	15	42559353	42559353	Human		name
405789276	CV3270017	single nucleotide variant	NM_018097.3(HAUS2):c.205C>T (p.Leu69Phe)	not specified [RCV004399193]	uncertain significance	15	42559357	42559357	Human		name
405789279	CV3270018	single nucleotide variant	NM_018097.3(HAUS2):c.232G>A (p.Asp78Asn)	not specified [RCV004399194]	uncertain significance	15	42559384	42559384	Human		name
597781249	CV3682168	single nucleotide variant	NM_018097.3(HAUS2):c.245C>T (p.Pro82Leu)	not specified [RCV004930847]	uncertain significance	15	42559397	42559397	Human		name
597709633	CV3682169	single nucleotide variant	NM_018097.3(HAUS2):c.254T>C (p.Leu85Ser)	not specified [RCV004917341]	uncertain significance	15	42559406	42559406	Human		name
597781254	CV3682170	single nucleotide variant	NM_018097.3(HAUS2):c.283A>T (p.Met95Leu)	not specified [RCV004930848]	uncertain significance	15	42561296	42561296	Human		name
598265488	CV3971411	single nucleotide variant	NM_018097.3(HAUS2):c.115A>C (p.Lys39Gln)	not specified [RCV005349068]	uncertain significance	15	42558219	42558219	Human		name
155981817	CV2244121	single nucleotide variant	NM_018097.3(HAUS2):c.571C>T (p.Arg191Cys)	not specified [RCV004108582]	uncertain significance	15	42566679	42566679	Human		name
156136152	CV2380055	single nucleotide variant	NM_018097.3(HAUS2):c.567G>C (p.Lys189Asn)	not specified [RCV004222187]	uncertain significance	15	42566675	42566675	Human		name
329358401	CV2450307	single nucleotide variant	NM_018097.3(HAUS2):c.481G>A (p.Ala161Thr)	not specified [RCV004271398]	uncertain significance	15	42563840	42563840	Human		name
401735622	CV2695360	single nucleotide variant	NM_018097.3(HAUS2):c.305T>C (p.Val102Ala)	not specified [RCV004305571]	uncertain significance	15	42561318	42561318	Human		name
405789287	CV3270020	single nucleotide variant	NM_018097.3(HAUS2):c.572G>A (p.Arg191His)	not specified [RCV004399196]	uncertain significance	15	42566680	42566680	Human		name
597781259	CV3682171	single nucleotide variant	NM_018097.3(HAUS2):c.637A>C (p.Lys213Gln)	not specified [RCV004930849]	uncertain significance	15	42566745	42566745	Human		name
598265494	CV3971412	single nucleotide variant	NM_018097.3(HAUS2):c.593C>T (p.Ser198Leu)	not specified [RCV005349069]	uncertain significance	15	42566701	42566701	Human		name

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