Prm2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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19 records found for search term Prm2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401911492	CV2807631	single nucleotide variant	NM_002762.4(PRM2):c.*4T>A	not provided [RCV003426588]	likely benign	16	11275896	11275896	Human		name
150483527	CV1263005	single nucleotide variant	NM_002762.4(PRM2):c.271+27G>C	not provided [RCV001686405]	benign	16	11276073	11276073	Human		name
150490255	CV1279575	single nucleotide variant	NM_002762.4(PRM2):c.272-61C>A	not provided [RCV001716436]	benign	16	11275998	11275998	Human		name
15200589	CV778362	single nucleotide variant	NM_002762.4(PRM2):c.271+10C>T	not provided [RCV000957374]	benign	16	11276090	11276090	Human		name
8584701	CV119277	single nucleotide variant	NM_001286356.1(PRM2):c.-1760C>T	Lung cancer [RCV000099797]	uncertain significance	16	11278130	11278130	Human		name
155994079	CV2379497	single nucleotide variant	NM_002762.4(PRM2):c.8G>A (p.Arg3Gln)	not specified [RCV004217213]	uncertain significance	16	11276363	11276363	Human		name
329367448	CV2456865	single nucleotide variant	NM_002762.4(PRM2):c.14G>A (p.Arg5His)	not specified [RCV004270827]	uncertain significance	16	11276357	11276357	Human		name
405671646	CV3377251	single nucleotide variant	NM_002762.4(PRM2):c.13C>T (p.Arg5Cys)	not specified [RCV004515284]	uncertain significance	16	11276358	11276358	Human		name
156090529	CV2206613	single nucleotide variant	NM_002762.4(PRM2):c.94G>A (p.Glu32Lys)	not specified [RCV004080954]	uncertain significance	16	11276277	11276277	Human		name
156248931	CV2277051	single nucleotide variant	NM_002762.4(PRM2):c.31G>A (p.Glu11Lys)	not specified [RCV004140371]	uncertain significance	16	11276340	11276340	Human		name
401859646	CV2771770	single nucleotide variant	NM_002762.4(PRM2):c.60G>T (p.Gln20His)	not specified [RCV004350548]	uncertain significance	16	11276311	11276311	Human		name
156275757	CV2209702	single nucleotide variant	NM_002762.4(PRM2):c.293C>G (p.Thr98Arg)	not specified [RCV004083027]	likely benign	16	11275916	11275916	Human		name
329377466	CV2453334	single nucleotide variant	NM_002762.4(PRM2):c.257G>A (p.Arg86Lys)	not specified [RCV004266960]	uncertain significance	16	11276114	11276114	Human		name
401726294	CV2695636	single nucleotide variant	NM_002762.4(PRM2):c.254G>A (p.Arg85Gln)	not specified [RCV004299452]	uncertain significance	16	11276117	11276117	Human		name
401730703	CV2711455	single nucleotide variant	NM_002762.4(PRM2):c.121G>A (p.Val41Ile)	not specified [RCV004306780]	uncertain significance	16	11276250	11276250	Human		name
401751197	CV2712449	single nucleotide variant	NM_002762.4(PRM2):c.229C>T (p.Arg77Cys)	not specified [RCV004313912]	uncertain significance	16	11276142	11276142	Human		name
405671651	CV3377252	single nucleotide variant	NM_002762.4(PRM2):c.161G>A (p.Arg54Lys)	not specified [RCV004515285]	uncertain significance	16	11276210	11276210	Human		name
405671656	CV3377253	single nucleotide variant	NM_002762.4(PRM2):c.185G>C (p.Arg62Thr)	not specified [RCV004515286]	uncertain significance	16	11276186	11276186	Human		name
597780609	CV3591893	single nucleotide variant	NM_002762.4(PRM2):c.205C>G (p.Arg69Gly)	not specified [RCV004853560]	uncertain significance	16	11276166	11276166	Human		name

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