Stat5a Variant Search Result - Rat Genome Database

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48 records found for search term Stat5a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15162265	CV778378	single nucleotide variant	NM_001288718.2(STAT5A):c.2063-4A>G	not provided [RCV000947823]	benign	17	42309043	42309043	Human		name
617149132	CV4021527	duplication	NM_001288718.2(STAT5A):c.2072_2114+2dup	not provided [RCV005425496]	uncertain significance	17	42309055	42309056	Human		name
156139722	CV2202926	single nucleotide variant	NM_001288718.2(STAT5A):c.27G>C (p.Gln9His)	not specified [RCV004069196]	uncertain significance	17	42289438	42289438	Human		name
15175312	CV740750	single nucleotide variant	NM_001288718.2(STAT5A):c.465G>A (p.Thr155=)	not provided [RCV000906183]	benign	17	42295708	42295708	Human		name
405739677	CV3334303	single nucleotide variant	NM_001288718.2(STAT5A):c.133G>T (p.Ala45Ser)	not specified [RCV004465516]	uncertain significance	17	42289870	42289870	Human		name
15168616	CV715458	single nucleotide variant	NM_001288718.2(STAT5A):c.2229C>T (p.Asp743=)	not provided [RCV000971650]	benign	17	42310513	42310513	Human		name
15147995	CV715459	single nucleotide variant	NM_001288718.2(STAT5A):c.2238C>T (p.Leu746=)	not provided [RCV000967454]	benign	17	42310522	42310522	Human		name
15192365	CV740751	single nucleotide variant	NM_001288718.2(STAT5A):c.1794G>C (p.Val598=)	not provided [RCV000910519]	benign	17	42307611	42307611	Human		name
155928477	CV2363291	single nucleotide variant	NM_001288718.2(STAT5A):c.581C>T (p.Pro194Leu)	not specified [RCV004213843]	uncertain significance	17	42299781	42299781	Human		name
156268695	CV2372081	single nucleotide variant	NM_001288718.2(STAT5A):c.881G>A (p.Arg294His)	not specified [RCV004221744]	uncertain significance	17	42300762	42300762	Human		name
156227873	CV2388346	single nucleotide variant	NM_001288718.2(STAT5A):c.944A>C (p.Glu315Ala)	not specified [RCV004234797]	uncertain significance	17	42300825	42300825	Human		name
329367829	CV2427580	single nucleotide variant	NM_001288718.2(STAT5A):c.563A>C (p.Gln188Pro)	not specified [RCV004250215]	likely benign	17	42299763	42299763	Human		name
329367831	CV2427581	single nucleotide variant	NM_001288718.2(STAT5A):c.560C>G (p.Ala187Gly)	not specified [RCV004250216]	likely benign	17	42299760	42299760	Human		name
401730193	CV2680035	single nucleotide variant	NM_001288718.2(STAT5A):c.341A>G (p.Tyr114Cys)	not specified [RCV004286534]	uncertain significance	17	42292027	42292027	Human		name
405740409	CV3334309	single nucleotide variant	NM_001288718.2(STAT5A):c.885G>C (p.Arg295Ser)	not specified [RCV004465522]	uncertain significance	17	42300766	42300766	Human		name
407496082	CV3485397	single nucleotide variant	NM_001288718.2(STAT5A):c.895C>T (p.Leu299Phe)	not specified [RCV004668031]	uncertain significance	17	42300776	42300776	Human		name
407496089	CV3485399	single nucleotide variant	NM_001288718.2(STAT5A):c.745G>A (p.Asp249Asn)	not specified [RCV004668033]	uncertain significance	17	42300193	42300193	Human		name
597703527	CV3618527	single nucleotide variant	NM_001288718.2(STAT5A):c.679G>A (p.Val227Met)	not specified [RCV004860203]	uncertain significance	17	42299879	42299879	Human		name
598213817	CV3919511	single nucleotide variant	NM_001288718.2(STAT5A):c.820G>A (p.Val274Met)	not specified [RCV005271103]	uncertain significance	17	42300268	42300268	Human		name
598251004	CV3919512	single nucleotide variant	NM_001288718.2(STAT5A):c.386C>T (p.Pro129Leu)	not specified [RCV005277804]	uncertain significance	17	42295629	42295629	Human		name
15147991	CV715457	single nucleotide variant	NM_001288718.2(STAT5A):c.626T>C (p.Val209Ala)	not provided [RCV000967453]	benign	17	42299826	42299826	Human		name
156061835	CV2240024	single nucleotide variant	NM_001288718.2(STAT5A):c.2152G>A (p.Ala718Thr)	not specified [RCV004110806]	uncertain significance	17	42309414	42309414	Human		name
156201186	CV2256137	single nucleotide variant	NM_001288718.2(STAT5A):c.1255A>G (p.Met419Val)	not specified [RCV004116417]	uncertain significance	17	42304427	42304427	Human		name
156073225	CV2263735	single nucleotide variant	NM_001288718.2(STAT5A):c.1072G>A (p.Gly358Arg)	not specified [RCV004136026]	uncertain significance	17	42301357	42301357	Human		name
156186746	CV2302733	single nucleotide variant	NM_001288718.2(STAT5A):c.1686C>G (p.Asn562Lys)	not specified [RCV004162661]	uncertain significance	17	42307407	42307407	Human		name
156357362	CV2318283	single nucleotide variant	NM_001288718.2(STAT5A):c.1277G>A (p.Arg426His)	not specified [RCV004179457]	uncertain significance	17	42304549	42304549	Human		name
156060412	CV2323093	single nucleotide variant	NM_001288718.2(STAT5A):c.1528G>A (p.Ala510Thr)	not specified [RCV004187508]	uncertain significance	17	42306295	42306295	Human		name
156361398	CV2326529	single nucleotide variant	NM_001288718.2(STAT5A):c.1734G>A (p.Met578Ile)	not specified [RCV004183082]	uncertain significance	17	42307455	42307455	Human		name
155907145	CV2389775	single nucleotide variant	NM_001288718.2(STAT5A):c.2344C>T (p.Pro782Ser)	not specified [RCV004236006]	uncertain significance	17	42310628	42310628	Human		name
401751292	CV2708551	single nucleotide variant	NM_001288718.2(STAT5A):c.2060T>G (p.Leu687Arg)	not specified [RCV004307547]	uncertain significance	17	42308331	42308331	Human		name
405739660	CV3334300	single nucleotide variant	NM_001288718.2(STAT5A):c.1057C>T (p.Arg353Cys)	not specified [RCV004465513]	uncertain significance	17	42301342	42301342	Human		name
405739666	CV3334301	single nucleotide variant	NM_001288718.2(STAT5A):c.1100C>G (p.Pro367Arg)	not specified [RCV004465514]	uncertain significance	17	42301385	42301385	Human		name
405739689	CV3334304	single nucleotide variant	NM_001288718.2(STAT5A):c.1363C>T (p.Leu455Phe)	not specified [RCV004465517]	uncertain significance	17	42304635	42304635	Human		name
405739694	CV3334305	single nucleotide variant	NM_001288718.2(STAT5A):c.1529C>T (p.Ala510Val)	not specified [RCV004465518]	uncertain significance	17	42306296	42306296	Human		name
405739700	CV3334306	single nucleotide variant	NM_001288718.2(STAT5A):c.2257G>A (p.Asp753Asn)	not specified [RCV004465519]	uncertain significance	17	42310541	42310541	Human		name
405739706	CV3334307	single nucleotide variant	NM_001288718.2(STAT5A):c.2314A>G (p.Met772Val)	not specified [RCV004465520]	uncertain significance	17	42310598	42310598	Human		name
405739712	CV3334308	single nucleotide variant	NM_001288718.2(STAT5A):c.2366C>T (p.Ala789Val)	not specified [RCV004465521]	uncertain significance	17	42310650	42310650	Human		name
407496084	CV3485398	single nucleotide variant	NM_001288718.2(STAT5A):c.1472C>G (p.Pro491Arg)	not specified [RCV004668032]	uncertain significance	17	42305701	42305701	Human		name
597747135	CV3618525	single nucleotide variant	NM_001288718.2(STAT5A):c.1092G>T (p.Met364Ile)	not specified [RCV004866007]	uncertain significance	17	42301377	42301377	Human		name
597703519	CV3618526	single nucleotide variant	NM_001288718.2(STAT5A):c.1513C>T (p.Pro505Ser)	not specified [RCV004860202]	uncertain significance	17	42306280	42306280	Human		name
597703537	CV3618528	single nucleotide variant	NM_001288718.2(STAT5A):c.2273T>C (p.Met758Thr)	not specified [RCV004860204]	uncertain significance	17	42310557	42310557	Human		name
598251009	CV3919513	single nucleotide variant	NM_001288718.2(STAT5A):c.1907C>T (p.Pro636Leu)	not specified [RCV005277805]	uncertain significance	17	42308178	42308178	Human		name
598251015	CV3919514	single nucleotide variant	NM_001288718.2(STAT5A):c.2197G>C (p.Ala733Pro)	not specified [RCV005277806]	uncertain significance	17	42309459	42309459	Human		name
598251022	CV3919515	single nucleotide variant	NM_001288718.2(STAT5A):c.1679G>A (p.Arg560Lys)	not specified [RCV005277807]	uncertain significance	17	42306446	42306446	Human		name
598251027	CV3919516	single nucleotide variant	NM_001288718.2(STAT5A):c.1360G>A (p.Glu454Lys)	not specified [RCV005277808]	uncertain significance	17	42304632	42304632	Human		name
598251034	CV3919517	single nucleotide variant	NM_001288718.2(STAT5A):c.2350G>A (p.Gly784Ser)	not specified [RCV005277809]	uncertain significance	17	42310634	42310634	Human		name
598251039	CV3919518	single nucleotide variant	NM_001288718.2(STAT5A):c.1291G>A (p.Gly431Ser)	not specified [RCV005277810]	uncertain significance	17	42304563	42304563	Human		name
15174136	CV679135	single nucleotide variant	NM_001288718.2(STAT5A):c.1279G>A (p.Ala427Thr)	Esophageal atresia [RCV000984687]	uncertain significance	17	42304551	42304551	Human	2	name

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