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Variants search result for Homo sapiens
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48 records found for search term Scmh1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156343568CV2364130single nucleotide variantNM_001394311.1(SCMH1):c.107-948G>Cnot specified [RCV004221506]uncertain significance14115263241152632Humanname
8575949CV110304single nucleotide variantNM_001031694.2(SCMH1):c.1468+496T>GLung cancer [RCV000090827]uncertain significance14104591141045911Humanname
401927589CV2812711single nucleotide variantNM_001394311.1(SCMH1):c.1668A>G (p.Leu556=)not provided [RCV003406403]likely benign14103737241037372Humanname
598197034CV3910366single nucleotide variantNM_001394311.1(SCMH1):c.160G>T (p.Val54Phe)not specified [RCV005268045]uncertain significance14115163141151631Humanname
598197047CV3910368single nucleotide variantNM_001394311.1(SCMH1):c.181T>A (p.Tyr61Asn)not specified [RCV005268047]uncertain significance14114310941143109Humanname
156240257CV2236025single nucleotide variantNM_001394311.1(SCMH1):c.373A>G (p.Asn125Asp)not specified [RCV004113891]uncertain significance14114291741142917Humanname
156292742CV2340252single nucleotide variantNM_001394311.1(SCMH1):c.428C>T (p.Ala143Val)not specified [RCV004194525]uncertain significance14111699541116995Humanname
155902669CV2386297single nucleotide variantNM_001394311.1(SCMH1):c.748G>T (p.Val250Leu)not specified [RCV004228642]uncertain significance14107544941075449Humanname
401744208CV2688117single nucleotide variantNM_001394311.1(SCMH1):c.862G>A (p.Gly288Arg)not specified [RCV004305170]uncertain significance14107533541075335Humanname
401724800CV2693423single nucleotide variantNM_001394311.1(SCMH1):c.947C>G (p.Pro316Arg)not specified [RCV004295374]uncertain significance14107525041075250Humanname
401876963CV2767778single nucleotide variantNM_001394311.1(SCMH1):c.458C>A (p.Thr153Lys)not specified [RCV004345904]uncertain significance14111696541116965Humanname
405744283CV3317342single nucleotide variantNM_001394311.1(SCMH1):c.474G>T (p.Glu158Asp)not specified [RCV004452863]uncertain significance14111694941116949Humanname
405744290CV3317343single nucleotide variantNM_001394311.1(SCMH1):c.668G>A (p.Arg223His)not specified [RCV004452864]uncertain significance14111336041113360Humanname
405744293CV3317344single nucleotide variantNM_001394311.1(SCMH1):c.746T>C (p.Val249Ala)not specified [RCV004452865]uncertain significance14107545141075451Humanname
597691656CV3597967single nucleotide variantNM_001394311.1(SCMH1):c.518C>G (p.Ser173Cys)not specified [RCV004858936]uncertain significance14111351041113510Humanname
597691664CV3597968single nucleotide variantNM_001394311.1(SCMH1):c.875G>T (p.Gly292Val)not specified [RCV004858937]uncertain significance14107532241075322Humanname
598196994CV3910360single nucleotide variantNM_001394311.1(SCMH1):c.802A>C (p.Ile268Leu)not specified [RCV005268039]uncertain significance14107539541075395Humanname
598197000CV3910361single nucleotide variantNM_001394311.1(SCMH1):c.596T>C (p.Ile199Thr)not specified [RCV005268040]uncertain significance14111343241113432Humanname
598197055CV3910369single nucleotide variantNM_001394311.1(SCMH1):c.667C>T (p.Arg223Cys)not specified [RCV005268048]uncertain significance14111336141113361Humanname
156374795CV2194834single nucleotide variantNM_001394311.1(SCMH1):c.1531C>T (p.Arg511Cys)not specified [RCV004075372]uncertain significance14103750941037509Humanname
156398893CV2194848single nucleotide variantNM_001394311.1(SCMH1):c.1558A>G (p.Met520Val)not specified [RCV004075382]uncertain significance14103748241037482Humanname
156398957CV2194894single nucleotide variantNM_001394311.1(SCMH1):c.1483G>A (p.Asp495Asn)not specified [RCV004075425]uncertain significance14104642241046422Humanname
156237007CV2206765single nucleotide variantNM_001394311.1(SCMH1):c.1751A>G (p.Asp584Gly)not specified [RCV004083450]uncertain significance14102872041028720Humanname
156271397CV2237189single nucleotide variantNM_001394311.1(SCMH1):c.1499G>T (p.Gly500Val)not specified [RCV004114929]uncertain significance14103754141037541Humanname
155955078CV2302361single nucleotide variantNM_001394311.1(SCMH1):c.1012G>A (p.Ala338Thr)not specified [RCV004161113]likely benign14107068841070688Humanname
156018479CV2302862single nucleotide variantNM_001394311.1(SCMH1):c.1276A>C (p.Lys426Gln)not specified [RCV004162761]uncertain significance14104872041048720Humanname
156154710CV2359641single nucleotide variantNM_001394311.1(SCMH1):c.1889A>G (p.Glu630Gly)not specified [RCV004210469]uncertain significance14102831841028318Humanname
156162947CV2389516single nucleotide variantNM_001394311.1(SCMH1):c.1366G>A (p.Val456Ile)not specified [RCV004243593]uncertain significance14104653941046539Humanname
329389167CV2448634single nucleotide variantNM_001394311.1(SCMH1):c.1444C>T (p.His482Tyr)not specified [RCV004259304]uncertain significance14104646141046461Humanname
329402531CV2454769single nucleotide variantNM_001394311.1(SCMH1):c.1628G>A (p.Cys543Tyr)not specified [RCV004270000]uncertain significance14103741241037412Humanname
401739812CV2709670single nucleotide variantNM_001394311.1(SCMH1):c.1413T>A (p.Asn471Lys)not specified [RCV004318880]uncertain significance14104649241046492Humanname
405744211CV3317332single nucleotide variantNM_001394311.1(SCMH1):c.1196G>A (p.Arg399His)not specified [RCV004452853]uncertain significance14104880041048800Humanname
405744222CV3317333single nucleotide variantNM_001394311.1(SCMH1):c.1261G>A (p.Val421Ile)not specified [RCV004452854]uncertain significance14104873541048735Humanname
405744228CV3317334single nucleotide variantNM_001394311.1(SCMH1):c.1462A>G (p.Ile488Val)not specified [RCV004452855]uncertain significance14104644341046443Humanname
405744235CV3317335single nucleotide variantNM_001394311.1(SCMH1):c.1613C>T (p.Pro538Leu)not specified [RCV004452856]uncertain significance14103742741037427Humanname
405744241CV3317336single nucleotide variantNM_001394311.1(SCMH1):c.1643G>A (p.Ser548Asn)not specified [RCV004452857]uncertain significance14103739741037397Humanname
405744247CV3317337single nucleotide variantNM_001394311.1(SCMH1):c.1764G>T (p.Glu588Asp)not specified [RCV004452858]uncertain significance14102870741028707Humanname
405744256CV3317338single nucleotide variantNM_001394311.1(SCMH1):c.1769G>T (p.Arg590Leu)not specified [RCV004452859]uncertain significance14102870241028702Humanname
405744263CV3317339single nucleotide variantNM_001394311.1(SCMH1):c.1991G>A (p.Arg664Gln)not specified [RCV004452860]uncertain significance14102821641028216Humanname
405744300CV3317345single nucleotide variantNM_001394311.1(SCMH1):c.1003C>G (p.Pro335Ala)not specified [RCV004452866]uncertain significance14107069741070697Humanname
407514475CV3480019single nucleotide variantNM_001394311.1(SCMH1):c.1793G>A (p.Arg598Gln)not specified [RCV004674567]uncertain significance14102867841028678Humanname
597691631CV3597965single nucleotide variantNM_001394311.1(SCMH1):c.1837C>T (p.Arg613Trp)not specified [RCV004858934]uncertain significance14102863441028634Humanname
597691643CV3597966single nucleotide variantNM_001394311.1(SCMH1):c.1769G>A (p.Arg590His)not specified [RCV004858935]uncertain significance14102870241028702Humanname
598197007CV3910362single nucleotide variantNM_001394311.1(SCMH1):c.2001G>C (p.Gln667His)not specified [RCV005268041]uncertain significance14102820641028206Humanname
598197015CV3910363single nucleotide variantNM_001394311.1(SCMH1):c.1660C>T (p.Arg554Cys)not specified [RCV005268042]uncertain significance14103738041037380Humanname
598197025CV3910365single nucleotide variantNM_001394311.1(SCMH1):c.1654G>A (p.Ala552Thr)not specified [RCV005268044]uncertain significance14103738641037386Humanname
598197040CV3910367single nucleotide variantNM_001394311.1(SCMH1):c.1102A>G (p.Thr368Ala)not specified [RCV005268046]uncertain significance14107059841070598Humanname
8629536CV84683single nucleotide variantNM_001031694.2(SCMH1):c.1762C>T (p.Arg588Trp)Malignant melanoma [RCV000064765]not provided14102867941028679Humanname