Pnma5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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23 records found for search term Pnma5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401921639	CV2824246	single nucleotide variant	NM_001184924.2(PNMA5):c.52A>G (p.Arg18Gly)	not provided [RCV003432557]	likely benign	X	152991547	152991547	Human		name
15112022	CV729463	single nucleotide variant	NM_001184924.2(PNMA5):c.900C>T (p.Pro300=)	not provided [RCV000894386]	benign	X	152990699	152990699	Human		name
15112029	CV729464	single nucleotide variant	NM_001184924.2(PNMA5):c.687C>T (p.Asp229=)	not provided [RCV000894387]	benign	X	152990912	152990912	Human		name
15195010	CV773842	single nucleotide variant	NM_001184924.2(PNMA5):c.939G>T (p.Gly313=)	not provided [RCV000933810]	benign	X	152990660	152990660	Human		name
401894830	CV2785356	single nucleotide variant	NM_001184924.2(PNMA5):c.896C>T (p.Thr299Ile)	not specified [RCV004357105]	uncertain significance	X	152990703	152990703	Human		name
405652385	CV3376532	single nucleotide variant	NM_001184924.2(PNMA5):c.941G>C (p.Cys314Ser)	not specified [RCV004509742]	uncertain significance	X	152990658	152990658	Human		name
156228250	CV2352892	single nucleotide variant	NM_001184924.2(PNMA5):c.1325A>G (p.His442Arg)	not specified [RCV004200939]	uncertain significance	X	152990274	152990274	Human		name
155999738	CV2373451	single nucleotide variant	NM_001184924.2(PNMA5):c.1312G>A (p.Gly438Arg)	not specified [RCV004220149]	uncertain significance	X	152990287	152990287	Human		name
156044154	CV2381608	single nucleotide variant	NM_001184924.2(PNMA5):c.1045C>T (p.Arg349Trp)	not specified [RCV004232081]	uncertain significance	X	152990554	152990554	Human		name
401863167	CV2772007	single nucleotide variant	NM_001184924.2(PNMA5):c.1174C>T (p.Arg392Cys)	not specified [RCV004344686]	uncertain significance	X	152990425	152990425	Human		name
405652381	CV3376530	single nucleotide variant	NM_001184924.2(PNMA5):c.1153G>A (p.Gly385Ser)	not specified [RCV004509740]	uncertain significance	X	152990446	152990446	Human		name
405652383	CV3376531	single nucleotide variant	NM_001184924.2(PNMA5):c.1291T>G (p.Leu431Val)	not specified [RCV004509741]	uncertain significance	X	152990308	152990308	Human		name
407524208	CV3463812	single nucleotide variant	NM_001184924.2(PNMA5):c.1193G>A (p.Ser398Asn)	not specified [RCV004653557]	uncertain significance	X	152990406	152990406	Human		name
597768730	CV3580651	single nucleotide variant	NM_001184924.2(PNMA5):c.1159C>A (p.Pro387Thr)	not specified [RCV004850749]	uncertain significance	X	152990440	152990440	Human		name
597743623	CV3580652	single nucleotide variant	NM_001184924.2(PNMA5):c.1235C>T (p.Pro412Leu)	not specified [RCV004845101]	uncertain significance	X	152990364	152990364	Human		name
597743630	CV3580653	single nucleotide variant	NM_001184924.2(PNMA5):c.1128C>A (p.Asp376Glu)	not specified [RCV004845102]	likely benign	X	152990471	152990471	Human		name
597743636	CV3580654	single nucleotide variant	NM_001184924.2(PNMA5):c.1208G>A (p.Gly403Glu)	not specified [RCV004845103]	likely benign	X	152990391	152990391	Human		name
598187417	CV4003482	single nucleotide variant	NM_001184924.2(PNMA5):c.1105G>A (p.Val369Met)	not specified [RCV005395916]	uncertain significance	X	152990494	152990494	Human		name
598187433	CV4003484	single nucleotide variant	NM_001184924.2(PNMA5):c.1283G>C (p.Gly428Ala)	not specified [RCV005395918]	uncertain significance	X	152990316	152990316	Human		name
598187440	CV4003485	single nucleotide variant	NM_001184924.2(PNMA5):c.1125C>G (p.Ser375Arg)	not specified [RCV005395919]	uncertain significance	X	152990474	152990474	Human		name
598187448	CV4003486	single nucleotide variant	NM_001184924.2(PNMA5):c.1303G>A (p.Ala435Thr)	not specified [RCV005395920]	uncertain significance	X	152990296	152990296	Human		name
598187457	CV4003487	single nucleotide variant	NM_001184924.2(PNMA5):c.1304C>T (p.Ala435Val)	not specified [RCV005395921]	uncertain significance	X	152990295	152990295	Human		name
15199770	CV758334	single nucleotide variant	NM_001184924.2(PNMA5):c.1252A>T (p.Thr418Ser)	not provided [RCV000912647]	benign	X	152990347	152990347	Human		name

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