Slc25a25 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 Slc25a25

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156091498	CV2216645	single nucleotide variant	NM_001330988.2(SLC25A25):c.188G>A (p.Gly63Asp)	not specified [RCV004083102]	uncertain significance	9	128068507	128068507	Human		name
15166818	CV723333	single nucleotide variant	NM_001330988.2(SLC25A25):c.1383G>A (p.Pro461=)	not provided [RCV000882715]	benign	9	128107279	128107279	Human		name
15183592	CV736893	single nucleotide variant	NM_001330988.2(SLC25A25):c.1377C>T (p.Gly459=)	not provided [RCV000908092]	likely benign	9	128107273	128107273	Human		name
156333721	CV2214650	single nucleotide variant	NM_001330988.2(SLC25A25):c.982G>A (p.Glu328Lys)	not specified [RCV004090478]	uncertain significance	9	128106195	128106195	Human		name
156272772	CV2247505	single nucleotide variant	NM_001330988.2(SLC25A25):c.944G>A (p.Arg315His)	not specified [RCV004108824]	uncertain significance	9	128106157	128106157	Human		name
156216269	CV2253755	single nucleotide variant	NM_001330988.2(SLC25A25):c.412A>T (p.Met138Leu)	not specified [RCV004127465]	uncertain significance	9	128101332	128101332	Human		name
155936798	CV2379908	single nucleotide variant	NM_001330988.2(SLC25A25):c.884A>G (p.Asn295Ser)	not specified [RCV004222057]	uncertain significance	9	128105829	128105829	Human		name
401761292	CV2706291	single nucleotide variant	NM_001330988.2(SLC25A25):c.644A>G (p.Asn215Ser)	not specified [RCV004314952]	uncertain significance	9	128103700	128103700	Human		name
401885327	CV2759685	single nucleotide variant	NM_001330988.2(SLC25A25):c.515T>C (p.Met172Thr)	not specified [RCV004340691]	uncertain significance	9	128102372	128102372	Human		name
401880261	CV2766180	single nucleotide variant	NM_001330988.2(SLC25A25):c.353G>A (p.Arg118Lys)	not specified [RCV004340623]	uncertain significance	9	128101187	128101187	Human		name
405767959	CV3325490	single nucleotide variant	NM_001330988.2(SLC25A25):c.796C>T (p.Arg266Cys)	not specified [RCV004456472]	uncertain significance	9	128105741	128105741	Human		name
405767966	CV3325491	single nucleotide variant	NM_001330988.2(SLC25A25):c.868C>T (p.Arg290Trp)	not specified [RCV004456473]	uncertain significance	9	128105813	128105813	Human		name
407509284	CV3473980	single nucleotide variant	NM_001330988.2(SLC25A25):c.580G>A (p.Val194Met)	not specified [RCV004672315]	uncertain significance	9	128102437	128102437	Human		name
407509292	CV3473982	single nucleotide variant	NM_001330988.2(SLC25A25):c.686C>T (p.Thr229Met)	not specified [RCV004672317]	uncertain significance	9	128103742	128103742	Human		name
597700382	CV3606304	single nucleotide variant	NM_001330988.2(SLC25A25):c.830C>T (p.Thr277Ile)	not specified [RCV004859859]	uncertain significance	9	128105775	128105775	Human		name
597700388	CV3606305	single nucleotide variant	NM_001330988.2(SLC25A25):c.875A>G (p.Asn292Ser)	not specified [RCV004859860]	uncertain significance	9	128105820	128105820	Human		name
598168676	CV3918189	single nucleotide variant	NM_001330988.2(SLC25A25):c.772G>A (p.Val258Met)	not specified [RCV005284137]	uncertain significance	9	128103828	128103828	Human		name
598168682	CV3918190	single nucleotide variant	NM_001330988.2(SLC25A25):c.323A>G (p.His108Arg)	not specified [RCV005284138]	uncertain significance	9	128101157	128101157	Human		name
598200347	CV3918192	single nucleotide variant	NM_001330988.2(SLC25A25):c.436G>A (p.Val146Ile)	not specified [RCV005268529]	uncertain significance	9	128101356	128101356	Human		name
14696176	CV612398	single nucleotide variant	NM_001330988.2(SLC25A25):c.481C>T (p.Arg161Ter)	High myopia [RCV000785723]	uncertain significance	9	128102084	128102084	Human	2	name
155921321	CV2207157	single nucleotide variant	NM_001330988.2(SLC25A25):c.1357G>A (p.Ala453Thr)	not specified [RCV004087896]	uncertain significance	9	128107173	128107173	Human		name
329401595	CV2457193	single nucleotide variant	NM_001330988.2(SLC25A25):c.1129G>C (p.Gly377Arg)	not specified [RCV004265275]	uncertain significance	9	128106437	128106437	Human		name
401774500	CV2691758	single nucleotide variant	NM_001330988.2(SLC25A25):c.1133T>G (p.Val378Gly)	not specified [RCV004299213]	uncertain significance	9	128106441	128106441	Human		name
405767951	CV3325488	single nucleotide variant	NM_001330988.2(SLC25A25):c.1541C>T (p.Ser514Leu)	not specified [RCV004456470]	uncertain significance	9	128107437	128107437	Human		name
407509287	CV3473981	single nucleotide variant	NM_001330988.2(SLC25A25):c.1058G>A (p.Arg353Gln)	not specified [RCV004672316]	uncertain significance	9	128106366	128106366	Human		name
597700373	CV3606303	single nucleotide variant	NM_001330988.2(SLC25A25):c.1264G>A (p.Gly422Ser)	not specified [RCV004859858]	uncertain significance	9	128107080	128107080	Human		name
598168688	CV3918191	single nucleotide variant	NM_001330988.2(SLC25A25):c.1070G>A (p.Arg357Gln)	not specified [RCV005284139]	uncertain significance	9	128106378	128106378	Human		name
40907052	CV969244	single nucleotide variant	NM_001330988.2(SLC25A25):c.1083G>C (p.Gln361His)	Nephrolithiasis [RCV001280533]	pathogenic	9	128106391	128106391	Human	2	name

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