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Variants search result for Homo sapiens
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25 records found for search term Dhrs11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156376354CV2210550single nucleotide variantNM_024308.4(DHRS11):c.5C>G (p.Ala2Gly)not specified [RCV004083362]uncertain significance173659201436592014Humanname
156321423CV2197579single nucleotide variantNM_024308.4(DHRS11):c.13G>C (p.Gly5Arg)not specified [RCV004081298]uncertain significance173659202236592022Humanname
156089059CV2392028single nucleotide variantNM_024308.4(DHRS11):c.14G>T (p.Gly5Val)not specified [RCV004235881]uncertain significance173659202336592023Humanname
597659095CV3655698single nucleotide variantNM_024308.4(DHRS11):c.25T>C (p.Trp9Arg)not specified [RCV004911592]uncertain significance173659203436592034Humanname
156027271CV2278419single nucleotide variantNM_024308.4(DHRS11):c.65G>A (p.Gly22Asp)not specified [RCV004132874]uncertain significance173659207436592074Humanname
156339698CV2351623single nucleotide variantNM_024308.4(DHRS11):c.50C>T (p.Thr17Met)not specified [RCV004195340]uncertain significance173659205936592059Humanname
405682250CV3247001single nucleotide variantNM_024308.4(DHRS11):c.34C>G (p.Arg12Gly)not specified [RCV004371397]uncertain significance173659204336592043Humanname
155996361CV2288501single nucleotide variantNM_024308.4(DHRS11):c.221A>G (p.Glu74Gly)not specified [RCV004152036]uncertain significance173659504436595044Humanname
156143329CV2393557single nucleotide variantNM_024308.4(DHRS11):c.232C>T (p.Leu78Phe)not specified [RCV004231375]uncertain significance173659505536595055Humanname
405682233CV3246998single nucleotide variantNM_024308.4(DHRS11):c.128G>T (p.Arg43Leu)not specified [RCV004371394]uncertain significance173659213736592137Humanname
405682239CV3246999single nucleotide variantNM_024308.4(DHRS11):c.137G>A (p.Gly46Asp)not specified [RCV004371395]uncertain significance173659214636592146Humanname
407467028CV3434051single nucleotide variantNM_024308.4(DHRS11):c.238A>G (p.Met80Val)not specified [RCV004614112]uncertain significance173659506136595061Humanname
407467032CV3434052single nucleotide variantNM_024308.4(DHRS11):c.269G>A (p.Gly90Asp)not specified [RCV004614113]uncertain significance173659509236595092Humanname
597659090CV3655697single nucleotide variantNM_024308.4(DHRS11):c.151C>G (p.Leu51Val)not specified [RCV004911591]uncertain significance173659497436594974Humanname
155971616CV2262355single nucleotide variantNM_024308.4(DHRS11):c.326G>A (p.Gly109Asp)not specified [RCV004128542]uncertain significance173659514936595149Humanname
156046625CV2390876single nucleotide variantNM_024308.4(DHRS11):c.517G>A (p.Val173Ile)not specified [RCV004234895]uncertain significance173659898536598985Humanname
401745465CV2698543single nucleotide variantNM_024308.4(DHRS11):c.376A>G (p.Ser126Gly)not specified [RCV004299033]uncertain significance173659818136598181Humanname
401776264CV2706945single nucleotide variantNM_024308.4(DHRS11):c.571A>G (p.Ile191Val)not specified [RCV004321550]uncertain significance173659903936599039Humanname
405682257CV3247002single nucleotide variantNM_024308.4(DHRS11):c.554G>A (p.Arg185Gln)not specified [RCV004371398]uncertain significance173659902236599022Humanname
405682260CV3247003single nucleotide variantNM_024308.4(DHRS11):c.616G>A (p.Ala206Thr)not specified [RCV004371399]uncertain significance173659970436599704Humanname
405682267CV3247004single nucleotide variantNM_024308.4(DHRS11):c.623A>G (p.Lys208Arg)not specified [RCV004371400]uncertain significance173659971136599711Humanname
405682272CV3247005single nucleotide variantNM_024308.4(DHRS11):c.722G>A (p.Ser241Asn)not specified [RCV004371401]uncertain significance173660001836600018Humanname
407467036CV3434053single nucleotide variantNM_024308.4(DHRS11):c.379A>G (p.Ile127Val)not specified [RCV004614114]uncertain significance173659818436598184Humanname
407467040CV3434054single nucleotide variantNM_024308.4(DHRS11):c.575G>A (p.Arg192Gln)not specified [RCV004614115]uncertain significance173659904336599043Humanname
597659101CV3655699single nucleotide variantNM_024308.4(DHRS11):c.332C>A (p.Thr111Asn)not specified [RCV004911593]uncertain significance173659515536595155Humanname