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27 records found for search term Tmem38a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156198341CV2334535single nucleotide variantNM_024074.4(TMEM38A):c.94G>C (p.Val32Leu)not specified [RCV004188495]uncertain significance191666131116661311Humanname
401877331CV2769417single nucleotide variantNM_024074.4(TMEM38A):c.55G>T (p.Val19Leu)not specified [RCV004357403]uncertain significance191666127216661272Humanname
8636661CV91886single nucleotide variantNM_024074.1(TMEM38A):c.348C>T (p.Leu116=)Malignant melanoma [RCV000071984]not provided191668046316680463Humanname
156397646CV2197359single nucleotide variantNM_024074.4(TMEM38A):c.142C>T (p.Arg48Trp)not specified [RCV004081101]uncertain significance191668000116680001Humanname
156212449CV2366950single nucleotide variantNM_024074.4(TMEM38A):c.146G>A (p.Arg49His)not specified [RCV004213356]uncertain significance191668000516680005Humanname
405755760CV3346506single nucleotide variantNM_024074.4(TMEM38A):c.249C>G (p.Asn83Lys)not specified [RCV004467797]uncertain significance191668010816680108Humanname
407526710CV3482733single nucleotide variantNM_024074.4(TMEM38A):c.118G>C (p.Glu40Gln)not specified [RCV004679736]uncertain significance191666133516661335Humanname
597764643CV3610493single nucleotide variantNM_024074.4(TMEM38A):c.175A>G (p.Met59Val)not specified [RCV004870191]uncertain significance191668003416680034Humanname
598226882CV3913898single nucleotide variantNM_024074.4(TMEM38A):c.194G>A (p.Ser65Asn)not specified [RCV005294492]uncertain significance191668005316680053Humanname
156062761CV2199785single nucleotide variantNM_024074.4(TMEM38A):c.382C>T (p.Arg128Cys)not specified [RCV004073988]uncertain significance191668049716680497Humanname
156226817CV2226520single nucleotide variantNM_024074.4(TMEM38A):c.697C>A (p.His233Asn)not specified [RCV004099713]uncertain significance191668816816688168Humanname
156310468CV2260046single nucleotide variantNM_024074.4(TMEM38A):c.478G>T (p.Ala160Ser)not specified [RCV004119056]uncertain significance191668243216682432Humanname
156151035CV2307525single nucleotide variantNM_024074.4(TMEM38A):c.537G>C (p.Glu179Asp)not specified [RCV004166170]uncertain significance191668249116682491Humanname
156045343CV2315517single nucleotide variantNM_024074.4(TMEM38A):c.733T>C (p.Cys245Arg)not specified [RCV004169568]uncertain significance191668820416688204Humanname
156192025CV2325673single nucleotide variantNM_024074.4(TMEM38A):c.893C>T (p.Ala298Val)not specified [RCV004180080]uncertain significance191668836416688364Humanname
156222134CV2343920single nucleotide variantNM_024074.4(TMEM38A):c.802G>A (p.Gly268Ser)not specified [RCV004195542]uncertain significance191668827316688273Humanname
329369499CV2424839single nucleotide variantNM_024074.4(TMEM38A):c.707C>G (p.Pro236Arg)not specified [RCV004248726]uncertain significance191668817816688178Humanname
329382684CV2445384single nucleotide variantNM_024074.4(TMEM38A):c.560C>T (p.Thr187Ile)not specified [RCV004257460]uncertain significance191668629316686293Humanname
329388034CV2468620single nucleotide variantNM_024074.4(TMEM38A):c.704C>A (p.Ser235Tyr)not specified [RCV004278177]uncertain significance191668817516688175Humanname
405755766CV3346507single nucleotide variantNM_024074.4(TMEM38A):c.355G>A (p.Val119Met)not specified [RCV004467798]uncertain significance191668047016680470Humanname
405755772CV3346508single nucleotide variantNM_024074.4(TMEM38A):c.506T>C (p.Leu169Pro)not specified [RCV004467799]uncertain significance191668246016682460Humanname
407526705CV3482731single nucleotide variantNM_024074.4(TMEM38A):c.485T>C (p.Met162Thr)not specified [RCV004679734]uncertain significance191668243916682439Humanname
407526707CV3482732single nucleotide variantNM_024074.4(TMEM38A):c.814G>A (p.Gly272Arg)not specified [RCV004679735]uncertain significance191668828516688285Humanname
597764635CV3610491single nucleotide variantNM_024074.4(TMEM38A):c.866G>A (p.Gly289Asp)not specified [RCV004870189]uncertain significance191668833716688337Humanname
597764639CV3610492single nucleotide variantNM_024074.4(TMEM38A):c.404A>G (p.His135Arg)not specified [RCV004870190]uncertain significance191668051916680519Humanname
598226876CV3913897single nucleotide variantNM_024074.4(TMEM38A):c.535G>A (p.Glu179Lys)not specified [RCV005294491]uncertain significance191668248916682489Humanname
598226890CV3913899single nucleotide variantNM_024074.4(TMEM38A):c.452C>T (p.Thr151Ile)not specified [RCV005294493]uncertain significance191668056716680567Humanname