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Variants search result for Homo sapiens
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63 records found for search term Cdh10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580774CV115206single nucleotide variantNM_006727.3(CDH10):c.1877-318C>GLung cancer [RCV000095729]uncertain significance52448847124488471Humanname
8580776CV115208single nucleotide variantNM_006727.3(CDH10):c.815-2357G>CLung cancer [RCV000095731]uncertain significance52451387124513871Humanname
8580778CV115210single nucleotide variantNM_006727.3(CDH10):c.231+4602T>ALung cancer [RCV000095733]uncertain significance52458865824588658Humanname
8580775CV115207single nucleotide variantNM_006727.3(CDH10):c.1393+2682C>GLung cancer [RCV000095730]uncertain significance52450243024502430Humanname
8580777CV115209single nucleotide variantNM_006727.3(CDH10):c.231+17927C>TLung cancer [RCV000095732]uncertain significance52457533324575333Humanname
156333286CV2266707single nucleotide variantNM_006727.5(CDH10):c.73A>G (p.Met25Val)not specified [RCV004137540]uncertain significance52459341824593418Humanname
15155704CV735062single nucleotide variantNM_006727.5(CDH10):c.510C>T (p.Pro170=)not provided [RCV000902191]benign52453739624537396Humanname
155797943CV1784573single nucleotide variantNM_006727.5(CDH10):c.151C>T (p.Arg51Cys)Lung cancer [RCV002465235]pathogenic52459334024593340Human1name
156253798CV2209593single nucleotide variantNM_006727.5(CDH10):c.137G>A (p.Gly46Asp)not specified [RCV004093690]uncertain significance52459335424593354Humanname
401925318CV2827673single nucleotide variantNM_006727.5(CDH10):c.1875G>A (p.Leu625=)not provided [RCV003436427]likely benign52449157724491577Humanname
401925319CV2827674single nucleotide variantNM_006727.5(CDH10):c.1416C>T (p.Arg472=)not provided [RCV003436428]likely benign52449849724498497Humanname
405719311CV3296374single nucleotide variantNM_006727.5(CDH10):c.121G>A (p.Val41Ile)not specified [RCV004427923]uncertain significance52459337024593370Humanname
597788581CV3645147single nucleotide variantNM_006727.5(CDH10):c.125C>T (p.Pro42Leu)not specified [RCV004901518]uncertain significance52459336624593366Humanname
15183671CV699056single nucleotide variantNM_006727.5(CDH10):c.2019C>T (p.Gly673=)not provided [RCV000952519]benign52448801124488011Humanname
15174534CV709866single nucleotide variantNM_006727.5(CDH10):c.1407G>A (p.Glu469=)not provided [RCV000972736]benign52449850624498506Humanname
8631596CV86800single nucleotide variantNM_006727.3(CDH10):c.253G>A (p.Gly85Arg)Malignant melanoma [RCV000066891]not provided52453765324537653Humanname
155797944CV1784574single nucleotide variantNM_006727.5(CDH10):c.583A>T (p.Ser195Cys)Lung cancer [RCV002465236]pathogenic52453576624535766Human1name
156268267CV2244198single nucleotide variantNM_006727.5(CDH10):c.491T>C (p.Ile164Thr)not specified [RCV004108643]uncertain significance52453741524537415Humanname
156356445CV2320788single nucleotide variantNM_006727.5(CDH10):c.544G>A (p.Val182Ile)not specified [RCV004172625]uncertain significance52453580524535805Humanname
156063569CV2331018single nucleotide variantNM_006727.5(CDH10):c.937G>A (p.Gly313Ser)not specified [RCV004188056]uncertain significance52451139224511392Humanname
156274624CV2334126single nucleotide variantNM_006727.5(CDH10):c.476C>T (p.Thr159Met)CDH10-related condition [RCV005356325]|not specified [RCV004183640]uncertain significance52453743024537430Humanname , trait
156402109CV2367993single nucleotide variantNM_006727.5(CDH10):c.969G>T (p.Lys323Asn)not specified [RCV004223082]uncertain significance52451136024511360Humanname
156305519CV2369497single nucleotide variantNM_006727.5(CDH10):c.874A>G (p.Lys292Glu)not specified [RCV004210434]uncertain significance52451145524511455Humanname
401720914CV2702189single nucleotide variantNM_006727.5(CDH10):c.827T>G (p.Leu276Arg)not specified [RCV004314538]uncertain significance52451150224511502Humanname
405719345CV3296378single nucleotide variantNM_006727.5(CDH10):c.637C>G (p.Pro213Ala)not specified [RCV004427927]uncertain significance52453571224535712Humanname
405719353CV3296379single nucleotide variantNM_006727.5(CDH10):c.802C>T (p.Arg268Cys)not specified [RCV004427928]uncertain significance52453512424535124Humanname
405719361CV3296380single nucleotide variantNM_006727.5(CDH10):c.832G>C (p.Val278Leu)not specified [RCV004427929]uncertain significance52451149724511497Humanname
405719372CV3296381single nucleotide variantNM_006727.5(CDH10):c.920G>A (p.Arg307Gln)not specified [RCV004427930]uncertain significance52451140924511409Humanname
407454770CV3422169single nucleotide variantNM_006727.5(CDH10):c.494A>G (p.Tyr165Cys)not specified [RCV004609983]uncertain significance52453741224537412Humanname
407499255CV3422170single nucleotide variantNM_006727.5(CDH10):c.899A>G (p.Lys300Arg)not specified [RCV004606838]uncertain significance52451143024511430Humanname
597788585CV3645148single nucleotide variantNM_006727.5(CDH10):c.530C>T (p.Thr177Ile)not specified [RCV004901519]uncertain significance52453581924535819Humanname
597788595CV3645151single nucleotide variantNM_006727.5(CDH10):c.863T>C (p.Ile288Thr)not specified [RCV004901522]uncertain significance52451146624511466Humanname
598210026CV3895016single nucleotide variantNM_006727.5(CDH10):c.948G>A (p.Met316Ile)CDH10-related condition [RCV005358476]uncertain significance52451138124511381Humanname , trait
8631595CV86799single nucleotide variantNM_006727.3(CDH10):c.700C>T (p.Gln234Ter)Malignant melanoma [RCV000066890]not provided52453522624535226Humanname
126910156CV1037634single nucleotide variantNM_006727.5(CDH10):c.1885G>A (p.Val629Ile)not provided [RCV001354411]uncertain significance52448814524488145Humanname
126912554CV1037635single nucleotide variantNM_006727.5(CDH10):c.1781A>G (p.Asn594Ser)not provided [RCV001356608]uncertain significance52449167124491671Humanname
126913497CV1037636single nucleotide variantNM_006727.5(CDH10):c.1394A>G (p.Asn465Ser)not provided [RCV001357419]uncertain significance52449851924498519Humanname
156234049CV2197168single nucleotide variantNM_006727.5(CDH10):c.1019G>A (p.Ser340Asn)not specified [RCV004071589]uncertain significance52450980324509803Humanname
156083090CV2249176single nucleotide variantNM_006727.5(CDH10):c.2042T>C (p.Ile681Thr)not specified [RCV004118223]uncertain significance52448798824487988Humanname
155991393CV2256440single nucleotide variantNM_006727.5(CDH10):c.1253T>G (p.Ile418Ser)not specified [RCV004118656]uncertain significance52450956924509569Humanname
156062237CV2277169single nucleotide variantNM_006727.5(CDH10):c.1441G>A (p.Asp481Asn)not specified [RCV004142811]uncertain significance52449847224498472Humanname
155962822CV2285699single nucleotide variantNM_006727.5(CDH10):c.2004G>C (p.Gln668His)not specified [RCV004141547]uncertain significance52448802624488026Humanname
156333016CV2335917single nucleotide variantNM_006727.5(CDH10):c.2297G>A (p.Arg766Gln)not specified [RCV004189530]uncertain significance52448773324487733Humanname
329391240CV2452175single nucleotide variantNM_006727.5(CDH10):c.1589C>T (p.Ala530Val)not specified [RCV004278886]uncertain significance52449285224492852Humanname
401759084CV2705370single nucleotide variantNM_006727.5(CDH10):c.1944A>C (p.Glu648Asp)not specified [RCV004312043]uncertain significance52448808624488086Humanname
401763913CV2725355single nucleotide variantNM_006727.5(CDH10):c.1073G>A (p.Arg358His)not specified [RCV004320007]uncertain significance52450974924509749Humanname
401892898CV2758199single nucleotide variantNM_006727.5(CDH10):c.1614G>C (p.Gln538His)not specified [RCV004341566]uncertain significance52449282724492827Humanname
401859377CV2771559single nucleotide variantNM_006727.5(CDH10):c.1022G>A (p.Arg341Gln)not specified [RCV004348583]uncertain significance52450980024509800Humanname
401877001CV2793312single nucleotide variantNM_006727.5(CDH10):c.1241T>C (p.Ile414Thr)not specified [RCV004362130]likely benign52450958124509581Humanname
405719316CV3296375single nucleotide variantNM_006727.5(CDH10):c.1750A>G (p.Ile584Val)not specified [RCV004427924]uncertain significance52449170224491702Humanname
405719328CV3296376single nucleotide variantNM_006727.5(CDH10):c.1880T>C (p.Ile627Thr)not specified [RCV004427925]uncertain significance52448815024488150Humanname
405719337CV3296377single nucleotide variantNM_006727.5(CDH10):c.2068A>G (p.Ile690Val)not specified [RCV004427926]uncertain significance52448796224487962Humanname
407499249CV3422168single nucleotide variantNM_006727.5(CDH10):c.2230A>G (p.Ile744Val)not specified [RCV004606837]uncertain significance52448780024487800Humanname
407499260CV3422171single nucleotide variantNM_006727.5(CDH10):c.1525A>G (p.Thr509Ala)not specified [RCV004606839]uncertain significance52449291624492916Humanname
407499265CV3422172single nucleotide variantNM_006727.5(CDH10):c.2243T>C (p.Leu748Pro)not specified [RCV004606840]uncertain significance52448778724487787Humanname
597788576CV3645146single nucleotide variantNM_006727.5(CDH10):c.2085A>T (p.Leu695Phe)not specified [RCV004901517]uncertain significance52448794524487945Humanname
597788589CV3645149single nucleotide variantNM_006727.5(CDH10):c.1351C>G (p.Leu451Val)not specified [RCV004901520]uncertain significance52450515424505154Humanname
597788592CV3645150single nucleotide variantNM_006727.5(CDH10):c.2042T>A (p.Ile681Asn)not specified [RCV004901521]uncertain significance52448798824487988Humanname
598168328CV3947267single nucleotide variantNM_006727.5(CDH10):c.2312G>A (p.Arg771Gln)not specified [RCV005308227]uncertain significance52448771824487718Humanname
598168334CV3947268single nucleotide variantNM_006727.5(CDH10):c.2186C>G (p.Pro729Arg)not specified [RCV005308228]uncertain significance52448784424487844Humanname
598168340CV3947269single nucleotide variantNM_006727.5(CDH10):c.1399C>T (p.Pro467Ser)not specified [RCV005308229]uncertain significance52449851424498514Humanname
8631593CV86797single nucleotide variantNM_006727.3(CDH10):c.2170G>A (p.Asp724Asn)Malignant melanoma [RCV000066888]not provided52448786024487860Humanname
8631594CV86798single nucleotide variantNM_006727.3(CDH10):c.1045G>A (p.Glu349Lys)Malignant melanoma [RCV000066889]not provided52450977724509777Humanname