Aldh3a1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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35 records found for search term Aldh3a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156181156	CV2384053	single nucleotide variant	NM_000691.5(ALDH3A1):c.5G>A (p.Ser2Asn)	not specified [RCV004225418]	uncertain significance	17	19745125	19745125	Human		name
15170153	CV704016	single nucleotide variant	NM_000691.5(ALDH3A1):c.258C>T (p.Pro86=)	not provided [RCV000949596]	benign	17	19743368	19743368	Human		name
15163735	CV727053	single nucleotide variant	NM_000691.5(ALDH3A1):c.141G>A (p.Ala47=)	not provided [RCV000882037]	benign	17	19744989	19744989	Human		name
401761293	CV2689097	single nucleotide variant	NM_000691.5(ALDH3A1):c.61C>T (p.Arg21Cys)	not specified [RCV004305862]	uncertain significance	17	19745069	19745069	Human		name
15173393	CV715289	single nucleotide variant	NM_000691.5(ALDH3A1):c.933C>T (p.Ala311=)	not provided [RCV000972600]	benign	17	19740352	19740352	Human		name
15163730	CV727052	single nucleotide variant	NM_000691.5(ALDH3A1):c.594G>A (p.Thr198=)	not provided [RCV000882036]	benign	17	19742099	19742099	Human		name
15140201	CV740645	single nucleotide variant	NM_000691.5(ALDH3A1):c.94G>A (p.Ala32Thr)	not provided [RCV000899277]	likely benign	17	19745036	19745036	Human		name
401866055	CV2762507	single nucleotide variant	NM_000691.5(ALDH3A1):c.129G>C (p.Glu43Asp)	not specified [RCV004338043]	likely benign	17	19745001	19745001	Human		name
405805013	CV3271228	single nucleotide variant	NM_000691.5(ALDH3A1):c.134T>G (p.Val45Gly)	not specified [RCV004405289]	uncertain significance	17	19744996	19744996	Human		name
15105477	CV755702	single nucleotide variant	NM_000691.5(ALDH3A1):c.1026C>T (p.Ile342=)	not provided [RCV000915555]	likely benign	17	19739598	19739598	Human		name
155981615	CV2208453	single nucleotide variant	NM_000691.5(ALDH3A1):c.934G>A (p.Ala312Thr)	not specified [RCV004090992]	uncertain significance	17	19740351	19740351	Human		name
156032765	CV2214515	single nucleotide variant	NM_000691.5(ALDH3A1):c.362C>T (p.Thr121Ile)	not specified [RCV004088569]	uncertain significance	17	19743264	19743264	Human		name
156332091	CV2220624	single nucleotide variant	NM_000691.5(ALDH3A1):c.925G>A (p.Gly309Arg)	not specified [RCV004097806]	uncertain significance	17	19740360	19740360	Human		name
156188563	CV2226776	single nucleotide variant	NM_000691.5(ALDH3A1):c.980A>C (p.Gln327Pro)	not specified [RCV004101992]	uncertain significance	17	19739644	19739644	Human		name
156106789	CV2257302	single nucleotide variant	NM_000691.5(ALDH3A1):c.623C>T (p.Thr208Met)	not specified [RCV004125407]	uncertain significance	17	19742070	19742070	Human		name
156046198	CV2268663	single nucleotide variant	NM_000691.5(ALDH3A1):c.764C>G (p.Ser255Trp)	not specified [RCV004124067]	uncertain significance	17	19741136	19741136	Human		name
156203178	CV2300705	single nucleotide variant	NM_000691.5(ALDH3A1):c.986C>T (p.Pro329Leu)	not specified [RCV004155643]	uncertain significance	17	19739638	19739638	Human		name
156343917	CV2349303	single nucleotide variant	NM_000691.5(ALDH3A1):c.416C>T (p.Pro139Leu)	not specified [RCV004199250]	uncertain significance	17	19742609	19742609	Human		name
243049306	CV2416514	single nucleotide variant	NM_000691.5(ALDH3A1):c.703G>A (p.Gly235Arg)	Keratoconus [RCV003150597]	likely pathogenic	17	19741197	19741197	Human	2	name
401727639	CV2678397	single nucleotide variant	NM_000691.5(ALDH3A1):c.521C>T (p.Thr174Met)	not specified [RCV004292425]	uncertain significance	17	19742172	19742172	Human		name
401779784	CV2714792	single nucleotide variant	NM_000691.5(ALDH3A1):c.382G>T (p.Ala128Ser)	not specified [RCV004320354]	uncertain significance	17	19743244	19743244	Human		name
405805039	CV3271242	single nucleotide variant	NM_000691.5(ALDH3A1):c.484C>G (p.Leu162Val)	not specified [RCV004405303]	uncertain significance	17	19742209	19742209	Human		name
405805054	CV3271250	single nucleotide variant	NM_000691.5(ALDH3A1):c.560C>T (p.Thr187Met)	not specified [RCV004405311]	uncertain significance	17	19742133	19742133	Human		name
405805082	CV3271265	single nucleotide variant	NM_000691.5(ALDH3A1):c.641A>G (p.Lys214Arg)	not specified [RCV004405326]	uncertain significance	17	19742052	19742052	Human		name
405805088	CV3271268	single nucleotide variant	NM_000691.5(ALDH3A1):c.859A>G (p.Ser287Gly)	not specified [RCV004405329]	uncertain significance	17	19740426	19740426	Human		name
407514524	CV3440142	single nucleotide variant	NM_000691.5(ALDH3A1):c.415C>T (p.Pro139Ser)	not specified [RCV004627537]	uncertain significance	17	19742610	19742610	Human		name
597705147	CV3688027	single nucleotide variant	NM_000691.5(ALDH3A1):c.349C>T (p.Pro117Ser)	not specified [RCV004916857]	uncertain significance	17	19743277	19743277	Human		name
598230066	CV3970091	single nucleotide variant	NM_000691.5(ALDH3A1):c.838C>T (p.Arg280Trp)	not specified [RCV005342180]	uncertain significance	17	19740447	19740447	Human		name
598158423	CV3970097	single nucleotide variant	NM_000691.5(ALDH3A1):c.614C>A (p.Thr205Asn)	not specified [RCV005328024]	uncertain significance	17	19742079	19742079	Human		name
15102916	CV704015	single nucleotide variant	NM_000691.5(ALDH3A1):c.899G>A (p.Gly300Asp)	not provided [RCV000959375]	benign	17	19740386	19740386	Human		name
15145552	CV755703	single nucleotide variant	NM_000691.5(ALDH3A1):c.697G>A (p.Ala233Thr)	not provided [RCV000922562]	likely benign	17	19741203	19741203	Human		name
329390145	CV2453513	single nucleotide variant	NM_000691.5(ALDH3A1):c.1181A>G (p.His394Arg)	not specified [RCV004269203]	uncertain significance	17	19739031	19739031	Human		name
401782066	CV2686512	single nucleotide variant	NM_000691.5(ALDH3A1):c.1075G>A (p.Glu359Lys)	not specified [RCV004299954]	uncertain significance	17	19739549	19739549	Human		name
597758791	CV3688023	single nucleotide variant	NM_000691.5(ALDH3A1):c.1262C>A (p.Thr421Asn)	not specified [RCV004925365]	uncertain significance	17	19738408	19738408	Human		name
598230121	CV3970106	single nucleotide variant	NM_000691.5(ALDH3A1):c.1357C>T (p.His453Tyr)	not specified [RCV005342193]	uncertain significance	17	19738226	19738226	Human		name

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