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Variants search result for Homo sapiens
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61 records found for search term Gprc5c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156156721CV2378593single nucleotide variantNM_022036.4(GPRC5C):c.-36G>Cnot specified [RCV004231074]uncertain significance177443213874432138Humanname
597694740CV3681718single nucleotide variantNM_022036.4(GPRC5C):c.-59G>Cnot specified [RCV004922532]uncertain significance177443211574432115Humanname
598274795CV3967452single nucleotide variantNM_022036.4(GPRC5C):c.-51G>Cnot specified [RCV005351586]uncertain significance177443212374432123Humanname
155945057CV2237925single nucleotide variantNM_022036.2(GPRC5C):c.5G>C (p.Arg2Pro)not specified [RCV004109147]uncertain significance177443204374432043Humanname
405740802CV3252221single nucleotide variantNM_022036.4(GPRC5C):c.27G>A (p.Met9Ile)not specified [RCV004391305]uncertain significance177443980374439803Humanname
155920919CV2276216single nucleotide variantNM_022036.4(GPRC5C):c.67G>A (p.Ala23Thr)not specified [RCV004142165]uncertain significance177443984374439843Humanname
405740822CV3252224single nucleotide variantNM_022036.2(GPRC5C):c.41G>A (p.Arg14Gln)not specified [RCV004391308]likely benign177443207974432079Humanname
597745702CV3681720single nucleotide variantNM_022036.4(GPRC5C):c.40C>T (p.Pro14Ser)not specified [RCV004922533]uncertain significance177443981674439816Humanname
597745711CV3681724single nucleotide variantNM_022036.4(GPRC5C):c.74G>A (p.Gly25Asp)not specified [RCV004922535]uncertain significance177443985074439850Humanname
401906545CV2808332single nucleotide variantNM_022036.4(GPRC5C):c.1323C>T (p.Asp441=)not provided [RCV003421468]likely benign177444702574447025Humanname
405740815CV3252223single nucleotide variantNM_022036.4(GPRC5C):c.176C>T (p.Ala59Val)not specified [RCV004391307]uncertain significance177443995274439952Humanname
597745716CV3681725single nucleotide variantNM_022036.4(GPRC5C):c.262G>A (p.Gly88Arg)not specified [RCV004922536]uncertain significance177444003874440038Humanname
598234203CV3967457single nucleotide variantNM_022036.4(GPRC5C):c.132C>A (p.Asp44Glu)not specified [RCV005342873]uncertain significance177443990874439908Humanname
15168250CV743608single nucleotide variantNM_022036.4(GPRC5C):c.205A>G (p.Ile69Val)not provided [RCV000904814]benign177443998174439981Humanname
156316301CV2193034single nucleotide variantNM_022036.4(GPRC5C):c.940G>T (p.Gly314Trp)not specified [RCV004069582]uncertain significance177444071674440716Humanname
156170857CV2197946single nucleotide variantNM_022036.4(GPRC5C):c.784A>C (p.Met262Leu)not specified [RCV004077160]uncertain significance177444056074440560Humanname
156090069CV2344603single nucleotide variantNM_022036.4(GPRC5C):c.425A>C (p.Asn142Thr)not specified [RCV004197376]uncertain significance177444020174440201Humanname
156239399CV2356343single nucleotide variantNM_022036.4(GPRC5C):c.334G>A (p.Asp112Asn)not specified [RCV004206147]uncertain significance177444011074440110Humanname
156074136CV2376950single nucleotide variantNM_022036.4(GPRC5C):c.958C>T (p.Arg320Trp)not specified [RCV004229638]uncertain significance177444073474440734Humanname
401757369CV2675264single nucleotide variantNM_022036.4(GPRC5C):c.478G>A (p.Ala160Thr)not specified [RCV004290031]uncertain significance177444025474440254Humanname
401766027CV2683502single nucleotide variantNM_022036.4(GPRC5C):c.749C>T (p.Ala250Val)not specified [RCV004288252]uncertain significance177444052574440525Humanname
401729155CV2690082single nucleotide variantNM_022036.4(GPRC5C):c.454C>T (p.Arg152Trp)not specified [RCV004300317]uncertain significance177444023074440230Humanname
401761633CV2699366single nucleotide variantNM_022036.4(GPRC5C):c.364C>T (p.Leu122Phe)not specified [RCV004305950]uncertain significance177444014074440140Humanname
405740828CV3252225single nucleotide variantNM_022036.4(GPRC5C):c.592G>A (p.Val198Met)not specified [RCV004391309]uncertain significance177444036874440368Humanname
405740834CV3252226single nucleotide variantNM_022036.4(GPRC5C):c.635C>G (p.Ala212Gly)not specified [RCV004391310]uncertain significance177444041174440411Humanname
405740842CV3252227single nucleotide variantNM_022036.4(GPRC5C):c.715C>T (p.Arg239Cys)not specified [RCV004391311]uncertain significance177444049174440491Humanname
405740851CV3252228single nucleotide variantNM_022036.4(GPRC5C):c.742A>G (p.Thr248Ala)not specified [RCV004391312]uncertain significance177444051874440518Humanname
405740858CV3252229single nucleotide variantNM_022036.4(GPRC5C):c.785T>C (p.Met262Thr)not specified [RCV004391313]uncertain significance177444056174440561Humanname
407526825CV3436848single nucleotide variantNM_022036.4(GPRC5C):c.757G>A (p.Val253Ile)not specified [RCV004632590]likely benign177444053374440533Humanname
407504577CV3436849single nucleotide variantNM_022036.4(GPRC5C):c.853G>A (p.Ala285Thr)not specified [RCV004624005]uncertain significance177444062974440629Humanname
407526828CV3436850single nucleotide variantNM_022036.4(GPRC5C):c.437G>A (p.Arg146Gln)not specified [RCV004632591]uncertain significance177444021374440213Humanname
407526837CV3436853single nucleotide variantNM_022036.4(GPRC5C):c.945C>A (p.Asp315Glu)not specified [RCV004632594]uncertain significance177444072174440721Humanname
597769941CV3681719single nucleotide variantNM_022036.4(GPRC5C):c.993G>C (p.Gln331His)not specified [RCV004928201]uncertain significance177444076974440769Humanname
597769950CV3681723single nucleotide variantNM_022036.4(GPRC5C):c.796G>A (p.Gly266Ser)not specified [RCV004928203]uncertain significance177444057274440572Humanname
597745724CV3681727single nucleotide variantNM_022036.4(GPRC5C):c.463G>A (p.Val155Met)not specified [RCV004922538]uncertain significance177444023974440239Humanname
597769955CV3681728single nucleotide variantNM_022036.4(GPRC5C):c.406G>A (p.Ala136Thr)not specified [RCV004928204]uncertain significance177444018274440182Humanname
598274789CV3967449single nucleotide variantNM_022036.4(GPRC5C):c.688G>A (p.Ala230Thr)not specified [RCV005351583]uncertain significance177444046474440464Humanname
598274791CV3967450single nucleotide variantNM_022036.4(GPRC5C):c.940G>A (p.Gly314Arg)not specified [RCV005351584]uncertain significance177444071674440716Humanname
598274793CV3967451single nucleotide variantNM_022036.4(GPRC5C):c.959G>A (p.Arg320Gln)not specified [RCV005351585]uncertain significance177444073574440735Humanname
598274797CV3967453single nucleotide variantNM_022036.4(GPRC5C):c.707A>G (p.Lys236Arg)not specified [RCV005351587]uncertain significance177444048374440483Humanname
598274799CV3967454single nucleotide variantNM_022036.4(GPRC5C):c.725G>C (p.Gly242Ala)not specified [RCV005351588]uncertain significance177444050174440501Humanname
598274800CV3967455single nucleotide variantNM_022036.4(GPRC5C):c.769G>T (p.Val257Leu)not specified [RCV005351589]uncertain significance177444054574440545Humanname
598234209CV3967458single nucleotide variantNM_022036.4(GPRC5C):c.971A>G (p.Tyr324Cys)not specified [RCV005342874]uncertain significance177444074774440747Humanname
598274804CV3967459single nucleotide variantNM_022036.4(GPRC5C):c.701G>A (p.Arg234His)not specified [RCV005351591]likely benign177444047774440477Humanname
598274806CV3967460single nucleotide variantNM_022036.4(GPRC5C):c.710G>T (p.Arg237Leu)not specified [RCV005351592]uncertain significance177444048674440486Humanname
598274807CV3967461single nucleotide variantNM_022036.4(GPRC5C):c.874G>A (p.Val292Ile)not specified [RCV005351593]uncertain significance177444065074440650Humanname
155961865CV2388139single nucleotide variantNM_022036.4(GPRC5C):c.1177C>T (p.Arg393Trp)not specified [RCV004241255]uncertain significance177444687974446879Humanname
329360945CV2439921single nucleotide variantNM_022036.4(GPRC5C):c.1270C>T (p.Pro424Ser)not specified [RCV004257955]uncertain significance177444697274446972Humanname
401773161CV2716475single nucleotide variantNM_022036.4(GPRC5C):c.1247C>G (p.Ala416Gly)not specified [RCV004325781]uncertain significance177444694974446949Humanname
401880031CV2769873single nucleotide variantNM_022036.4(GPRC5C):c.1274C>T (p.Pro425Leu)not specified [RCV004353723]likely benign177444697674446976Humanname
401876282CV2789222single nucleotide variantNM_022036.4(GPRC5C):c.1058G>A (p.Arg353Lys)not specified [RCV004365257]uncertain significance177444382474443824Humanname
401898925CV2792125single nucleotide variantNM_022036.4(GPRC5C):c.1271C>A (p.Pro424Gln)not specified [RCV004361347]uncertain significance177444697374446973Humanname
401916614CV2808331single nucleotide variantNM_022036.4(GPRC5C):c.1144C>A (p.Pro382Thr)not provided [RCV003429146]likely benign177444391074443910Humanname
405740766CV3252216single nucleotide variantNM_022036.4(GPRC5C):c.1078G>A (p.Gly360Arg)not specified [RCV004391300]uncertain significance177444384474443844Humanname
405740774CV3252217single nucleotide variantNM_022036.4(GPRC5C):c.1085A>G (p.Asn362Ser)not specified [RCV004391301]uncertain significance177444385174443851Humanname
405740781CV3252218single nucleotide variantNM_022036.4(GPRC5C):c.1150G>A (p.Glu384Lys)not specified [RCV004391302]uncertain significance177444685274446852Humanname
405740788CV3252219single nucleotide variantNM_022036.4(GPRC5C):c.1225C>T (p.Arg409Trp)not specified [RCV004391303]uncertain significance177444692774446927Humanname
405740795CV3252220single nucleotide variantNM_022036.4(GPRC5C):c.1250A>G (p.Gln417Arg)not specified [RCV004391304]uncertain significance177444695274446952Humanname
597745706CV3681721single nucleotide variantNM_022036.4(GPRC5C):c.1193G>A (p.Ser398Asn)not specified [RCV004922534]uncertain significance177444689574446895Humanname
597769946CV3681722single nucleotide variantNM_022036.4(GPRC5C):c.1043C>T (p.Pro348Leu)not specified [RCV004928202]uncertain significance177444081974440819Humanname
597745720CV3681726single nucleotide variantNM_022036.4(GPRC5C):c.1024G>T (p.Ala342Ser)not specified [RCV004922537]uncertain significance177444080074440800Humanname