Pnn Variant Search Result - Rat Genome Database

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64 records found for search term Pnn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15105678	CV779624	single nucleotide variant	NM_002687.4(PNN):c.185+10C>T	not provided [RCV000959932]	benign	14	39176159	39176159	Human		name
329353895	CV2439933	single nucleotide variant	NM_002687.4(PNN):c.8T>C (p.Val3Ala)	not specified [RCV004257966]	uncertain significance	14	39175287	39175287	Human		name
405652460	CV3376594	single nucleotide variant	NM_002687.4(PNN):c.11C>T (p.Ala4Val)	not specified [RCV004509804]	uncertain significance	14	39175290	39175290	Human		name
597743795	CV3590632	single nucleotide variant	NM_002687.4(PNN):c.85C>T (p.Leu29Phe)	not specified [RCV004845132]	uncertain significance	14	39175364	39175364	Human		name
15163388	CV714123	single nucleotide variant	NM_002687.4(PNN):c.553A>C (p.Arg185=)	not provided [RCV000970474]	benign\|likely benign	14	39179145	39179145	Human		name
597743813	CV3590635	single nucleotide variant	NM_002687.4(PNN):c.217C>T (p.Pro73Ser)	not specified [RCV004845135]	uncertain significance	14	39176558	39176558	Human		name
597743829	CV3590638	single nucleotide variant	NM_002687.4(PNN):c.259G>A (p.Gly87Ser)	not specified [RCV004845138]	uncertain significance	14	39177416	39177416	Human		name
598187624	CV4003511	single nucleotide variant	NM_002687.4(PNN):c.200A>T (p.Asp67Val)	not specified [RCV005395945]	uncertain significance	14	39176541	39176541	Human		name
598187644	CV4003514	single nucleotide variant	NM_002687.4(PNN):c.164G>A (p.Gly55Glu)	not specified [RCV005395948]	uncertain significance	14	39176128	39176128	Human		name
15160835	CV702869	single nucleotide variant	NM_002687.4(PNN):c.1872C>T (p.Ser624=)	not provided [RCV000947563]	benign	14	39181581	39181581	Human		name
156107374	CV2214162	single nucleotide variant	NM_002687.4(PNN):c.748C>A (p.Pro250Thr)	not specified [RCV004086160]	uncertain significance	14	39179417	39179417	Human		name
156269498	CV2326385	single nucleotide variant	NM_002687.4(PNN):c.373C>T (p.Arg125Cys)	not specified [RCV004182962]	uncertain significance	14	39177638	39177638	Human		name
155995520	CV2375825	single nucleotide variant	NM_002687.4(PNN):c.948G>T (p.Glu316Asp)	not specified [RCV004224405]	uncertain significance	14	39180657	39180657	Human		name
156391061	CV2385057	single nucleotide variant	NM_002687.4(PNN):c.766A>G (p.Ile256Val)	not specified [RCV004228322]	uncertain significance	14	39179435	39179435	Human		name
401745279	CV2698505	single nucleotide variant	NM_002687.4(PNN):c.331G>A (p.Ala111Thr)	not specified [RCV004299003]	uncertain significance	14	39177596	39177596	Human		name
407524110	CV3463830	single nucleotide variant	NM_002687.4(PNN):c.896G>A (p.Arg299His)	not specified [RCV004653563]	uncertain significance	14	39180605	39180605	Human		name
597743784	CV3590630	single nucleotide variant	NM_002687.4(PNN):c.557A>G (p.Lys186Arg)	not specified [RCV004845130]	uncertain significance	14	39179149	39179149	Human		name
597743807	CV3590634	single nucleotide variant	NM_002687.4(PNN):c.496A>G (p.Arg166Gly)	not specified [RCV004845134]	uncertain significance	14	39177914	39177914	Human		name
597743973	CV3590642	single nucleotide variant	NM_002687.4(PNN):c.389A>G (p.Gln130Arg)	not specified [RCV004845142]	uncertain significance	14	39177654	39177654	Human		name
597743977	CV3590643	single nucleotide variant	NM_002687.4(PNN):c.636A>C (p.Lys212Asn)	not specified [RCV004845143]	uncertain significance	14	39179228	39179228	Human		name
598187654	CV4003516	single nucleotide variant	NM_002687.4(PNN):c.763C>G (p.Leu255Val)	not specified [RCV005395950]	uncertain significance	14	39179432	39179432	Human		name
598187660	CV4003517	single nucleotide variant	NM_002687.4(PNN):c.428G>A (p.Arg143Gln)	not specified [RCV005395951]	uncertain significance	14	39177846	39177846	Human		name
156375835	CV2210327	single nucleotide variant	NM_002687.4(PNN):c.1592C>T (p.Pro531Leu)	not specified [RCV004089484]	uncertain significance	14	39181301	39181301	Human		name
156223303	CV2232949	single nucleotide variant	NM_002687.4(PNN):c.1585G>A (p.Asp529Asn)	not specified [RCV004103328]	uncertain significance	14	39181294	39181294	Human		name
156085749	CV2244639	single nucleotide variant	NM_002687.4(PNN):c.1813A>G (p.Ser605Gly)	not specified [RCV004102355]	uncertain significance	14	39181522	39181522	Human		name
155914707	CV2264627	single nucleotide variant	NM_002687.4(PNN):c.2135G>A (p.Arg712Lys)	not specified [RCV004132632]	uncertain significance	14	39181844	39181844	Human		name
156295820	CV2297509	single nucleotide variant	NM_002687.4(PNN):c.1480C>G (p.Leu494Val)	not specified [RCV004153435]	uncertain significance	14	39181189	39181189	Human		name
156050528	CV2323282	single nucleotide variant	NM_002687.4(PNN):c.2096A>C (p.Lys699Thr)	not specified [RCV004171698]	uncertain significance	14	39181805	39181805	Human		name
155913317	CV2341753	single nucleotide variant	NM_002687.4(PNN):c.1360A>G (p.Met454Val)	not specified [RCV004182667]	uncertain significance	14	39181069	39181069	Human		name
156385486	CV2364478	single nucleotide variant	NM_002687.4(PNN):c.2056G>A (p.Asp686Asn)	not specified [RCV004217348]	uncertain significance	14	39181765	39181765	Human		name
156096046	CV2375275	single nucleotide variant	NM_002687.4(PNN):c.1262C>T (p.Ala421Val)	not specified [RCV004232685]	uncertain significance	14	39180971	39180971	Human		name
156092812	CV2381963	single nucleotide variant	NM_002687.4(PNN):c.2087G>A (p.Arg696Gln)	not specified [RCV004225895]	uncertain significance	14	39181796	39181796	Human		name
329373475	CV2434217	single nucleotide variant	NM_002687.4(PNN):c.1383A>C (p.Lys461Asn)	not specified [RCV004250104]	uncertain significance	14	39181092	39181092	Human		name
329400887	CV2449711	single nucleotide variant	NM_002687.4(PNN):c.1160T>C (p.Met387Thr)	not specified [RCV004268611]	uncertain significance	14	39180869	39180869	Human		name
329391119	CV2452049	single nucleotide variant	NM_002687.4(PNN):c.1553A>G (p.Gln518Arg)	not specified [RCV004278779]	uncertain significance	14	39181262	39181262	Human		name
329361356	CV2459420	single nucleotide variant	NM_002687.4(PNN):c.2009G>T (p.Gly670Val)	not specified [RCV004275110]	uncertain significance	14	39181718	39181718	Human		name
329396217	CV2459421	single nucleotide variant	NM_002687.4(PNN):c.2030G>A (p.Gly677Glu)	not specified [RCV004275111]	uncertain significance	14	39181739	39181739	Human		name
329396851	CV2468261	single nucleotide variant	NM_002687.4(PNN):c.1028C>T (p.Ala343Val)	not specified [RCV004275823]	uncertain significance	14	39180737	39180737	Human		name
401731388	CV2674356	single nucleotide variant	NM_002687.4(PNN):c.1610T>C (p.Leu537Pro)	not specified [RCV004289229]	uncertain significance	14	39181319	39181319	Human		name
401772722	CV2687791	single nucleotide variant	NM_002687.4(PNN):c.1261G>C (p.Ala421Pro)	not specified [RCV004302773]	uncertain significance	14	39180970	39180970	Human		name
401731415	CV2701354	single nucleotide variant	NM_002687.4(PNN):c.2079G>C (p.Glu693Asp)	not specified [RCV004311727]	uncertain significance	14	39181788	39181788	Human		name
401768612	CV2716672	single nucleotide variant	NM_002687.4(PNN):c.1162G>A (p.Asp388Asn)	not specified [RCV004327728]	uncertain significance	14	39180871	39180871	Human		name
401746803	CV2731970	single nucleotide variant	NM_002687.4(PNN):c.1564C>T (p.His522Tyr)	not specified [RCV004333206]	uncertain significance	14	39181273	39181273	Human		name
405652456	CV3376592	single nucleotide variant	NM_002687.4(PNN):c.1040G>T (p.Ser347Ile)	not specified [RCV004509802]	uncertain significance	14	39180749	39180749	Human		name
405652458	CV3376593	single nucleotide variant	NM_002687.4(PNN):c.1102G>A (p.Glu368Lys)	not specified [RCV004509803]	uncertain significance	14	39180811	39180811	Human		name
405652463	CV3376595	single nucleotide variant	NM_002687.4(PNN):c.1421C>T (p.Ala474Val)	not specified [RCV004509805]	uncertain significance	14	39181130	39181130	Human		name
405652465	CV3376596	single nucleotide variant	NM_002687.4(PNN):c.1528T>G (p.Leu510Val)	not specified [RCV004509806]	uncertain significance	14	39181237	39181237	Human		name
405652467	CV3376597	single nucleotide variant	NM_002687.4(PNN):c.1763C>T (p.Thr588Ile)	not specified [RCV004509807]	uncertain significance	14	39181472	39181472	Human		name
405652469	CV3376598	single nucleotide variant	NM_002687.4(PNN):c.1874C>T (p.Thr625Ile)	not specified [RCV004509808]	uncertain significance	14	39181583	39181583	Human		name
405652471	CV3376599	single nucleotide variant	NM_002687.4(PNN):c.1888G>A (p.Glu630Lys)	not specified [RCV004509809]	uncertain significance	14	39181597	39181597	Human		name
405652473	CV3376600	single nucleotide variant	NM_002687.4(PNN):c.1955G>A (p.Arg652Gln)	not specified [RCV004509810]	uncertain significance	14	39181664	39181664	Human		name
405652523	CV3376601	single nucleotide variant	NM_002687.4(PNN):c.2073A>G (p.Ile691Met)	not specified [RCV004509811]	uncertain significance	14	39181782	39181782	Human		name
407524107	CV3463829	single nucleotide variant	NM_002687.4(PNN):c.2095A>C (p.Lys699Gln)	not specified [RCV004653562]	uncertain significance	14	39181804	39181804	Human		name
407524113	CV3463831	single nucleotide variant	NM_002687.4(PNN):c.1508A>G (p.Glu503Gly)	not specified [RCV004653564]	uncertain significance	14	39181217	39181217	Human		name
407471916	CV3463832	single nucleotide variant	NM_002687.4(PNN):c.1055A>T (p.Glu352Val)	not specified [RCV004662396]	uncertain significance	14	39180764	39180764	Human		name
597743789	CV3590631	single nucleotide variant	NM_002687.4(PNN):c.2050C>T (p.Arg684Trp)	not specified [RCV004845131]	uncertain significance	14	39181759	39181759	Human		name
597743801	CV3590633	single nucleotide variant	NM_002687.4(PNN):c.1139A>G (p.Asp380Gly)	not specified [RCV004845133]	uncertain significance	14	39180848	39180848	Human		name
597743817	CV3590636	single nucleotide variant	NM_002687.4(PNN):c.1924A>G (p.Arg642Gly)	not specified [RCV004845136]	uncertain significance	14	39181633	39181633	Human		name
597743958	CV3590639	single nucleotide variant	NM_002687.4(PNN):c.1663A>G (p.Lys555Glu)	not specified [RCV004845139]	uncertain significance	14	39181372	39181372	Human		name
597743963	CV3590640	single nucleotide variant	NM_002687.4(PNN):c.2057A>G (p.Asp686Gly)	not specified [RCV004845140]	uncertain significance	14	39181766	39181766	Human		name
597743968	CV3590641	single nucleotide variant	NM_002687.4(PNN):c.1752T>A (p.Ser584Arg)	not specified [RCV004845141]	uncertain significance	14	39181461	39181461	Human		name
598187630	CV4003512	single nucleotide variant	NM_002687.4(PNN):c.1325T>A (p.Leu442His)	not specified [RCV005395946]	uncertain significance	14	39181034	39181034	Human		name
598187648	CV4003515	single nucleotide variant	NM_002687.4(PNN):c.1948G>T (p.Val650Leu)	not specified [RCV005395949]	uncertain significance	14	39181657	39181657	Human		name
15141004	CV714124	single nucleotide variant	NM_002687.4(PNN):c.1576G>A (p.Glu526Lys)	not provided [RCV000966236]	benign	14	39181285	39181285	Human		name

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