Nanp Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Nanp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597654290	CV3565147	single nucleotide variant	NM_152667.3(NANP):c.19C>T (p.Arg7Trp)	not specified [RCV004834057]	uncertain significance	20	25623930	25623930	Human		name
598205160	CV3987219	single nucleotide variant	NM_152667.3(NANP):c.16G>C (p.Val6Leu)	not specified [RCV005376716]	uncertain significance	20	25623933	25623933	Human		name
156235955	CV2346403	single nucleotide variant	NM_152667.3(NANP):c.65G>A (p.Gly22Glu)	not specified [RCV004203881]	uncertain significance	20	25623884	25623884	Human		name
156281585	CV2348790	single nucleotide variant	NM_152667.3(NANP):c.139A>C (p.Ile47Leu)	not specified [RCV004203237]	uncertain significance	20	25616533	25616533	Human		name
407520721	CV3447926	single nucleotide variant	NM_152667.3(NANP):c.226T>G (p.Trp76Gly)	not specified [RCV004652281]	uncertain significance	20	25616446	25616446	Human		name
597654274	CV3565145	single nucleotide variant	NM_152667.3(NANP):c.194A>G (p.Asn65Ser)	not specified [RCV004834055]	likely benign	20	25616478	25616478	Human		name
598205147	CV3987217	single nucleotide variant	NM_152667.3(NANP):c.239T>C (p.Ile80Thr)	not specified [RCV005376714]	uncertain significance	20	25616433	25616433	Human		name
156131224	CV2279918	single nucleotide variant	NM_152667.3(NANP):c.482G>A (p.Arg161Lys)	not specified [RCV004146295]	likely benign	20	25616190	25616190	Human		name
156188372	CV2375340	single nucleotide variant	NM_152667.3(NANP):c.532G>A (p.Gly178Arg)	not specified [RCV004232741]	uncertain significance	20	25616140	25616140	Human		name
329388977	CV2469672	single nucleotide variant	NM_152667.3(NANP):c.311G>A (p.Arg104His)	not specified [RCV004283087]	uncertain significance	20	25616361	25616361	Human		name
405791102	CV3335341	single nucleotide variant	NM_152667.3(NANP):c.608T>G (p.Leu203Trp)	not specified [RCV004474103]	uncertain significance	20	25616064	25616064	Human		name
407487821	CV3447927	single nucleotide variant	NM_152667.3(NANP):c.587A>T (p.Gln196Leu)	not specified [RCV004641173]	uncertain significance	20	25616085	25616085	Human		name
597654281	CV3565146	single nucleotide variant	NM_152667.3(NANP):c.662C>T (p.Pro221Leu)	not specified [RCV004834056]	uncertain significance	20	25616010	25616010	Human		name
597654298	CV3565148	single nucleotide variant	NM_152667.3(NANP):c.677T>C (p.Met226Thr)	not specified [RCV004834058]	uncertain significance	20	25615995	25615995	Human		name
598205153	CV3987218	single nucleotide variant	NM_152667.3(NANP):c.500C>T (p.Pro167Leu)	not specified [RCV005376715]	uncertain significance	20	25616172	25616172	Human		name