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18 records found for search term Tmem69
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405772049CV3346688single nucleotide variantNM_016486.4(TMEM69):c.98C>G (p.Ser33Cys)not specified [RCV004470459]uncertain significance14569325945693259Humanname
598227449CV3914027single nucleotide variantNM_016486.4(TMEM69):c.92T>C (p.Ile31Thr)not specified [RCV005294590]likely benign14569325345693253Humanname
156270147CV2305966single nucleotide variantNM_016486.4(TMEM69):c.113T>C (p.Leu38Pro)not specified [RCV004169527]uncertain significance14569327445693274Humanname
155910542CV2366491single nucleotide variantNM_016486.4(TMEM69):c.148C>T (p.Leu50Phe)not specified [RCV004208467]uncertain significance14569330945693309Humanname
401761003CV2726610single nucleotide variantNM_016486.4(TMEM69):c.266A>C (p.Tyr89Ser)not specified [RCV004329095]uncertain significance14569342745693427Humanname
405772026CV3346684single nucleotide variantNM_016486.4(TMEM69):c.290C>T (p.Ala97Val)not specified [RCV004470455]uncertain significance14569345145693451Humanname
156238535CV2221180single nucleotide variantNM_016486.4(TMEM69):c.632T>A (p.Phe211Tyr)not specified [RCV004094626]uncertain significance14569379345693793Humanname
156072563CV2289986single nucleotide variantNM_016486.4(TMEM69):c.499G>T (p.Ala167Ser)not specified [RCV004150631]uncertain significance14569366045693660Humanname
156079347CV2341249single nucleotide variantNM_016486.4(TMEM69):c.325G>A (p.Val109Ile)not specified [RCV004186662]likely benign14569348645693486Humanname
156229304CV2352975single nucleotide variantNM_016486.4(TMEM69):c.475T>C (p.Tyr159His)not specified [RCV004201010]uncertain significance14569363645693636Humanname
155968805CV2391502single nucleotide variantNM_016486.4(TMEM69):c.368C>T (p.Pro123Leu)not specified [RCV004239888]uncertain significance14569352945693529Humanname
329361267CV2459563single nucleotide variantNM_016486.4(TMEM69):c.500C>T (p.Ala167Val)not specified [RCV004277016]uncertain significance14569366145693661Humanname
401870455CV2769261single nucleotide variantNM_016486.4(TMEM69):c.617A>C (p.His206Pro)not specified [RCV004357273]uncertain significance14569377845693778Humanname
405772031CV3346685single nucleotide variantNM_016486.4(TMEM69):c.340G>T (p.Val114Phe)not specified [RCV004470456]uncertain significance14569350145693501Humanname
405772037CV3346686single nucleotide variantNM_016486.4(TMEM69):c.362A>G (p.Tyr121Cys)not specified [RCV004470457]uncertain significance14569352345693523Humanname
405772042CV3346687single nucleotide variantNM_016486.4(TMEM69):c.700A>T (p.Ser234Cys)not specified [RCV004470458]uncertain significance14569386145693861Humanname
597800637CV3610662single nucleotide variantNM_016486.4(TMEM69):c.466A>C (p.Lys156Gln)not specified [RCV004880312]uncertain significance14569362745693627Humanname
597800639CV3610663single nucleotide variantNM_016486.4(TMEM69):c.390G>A (p.Met130Ile)not specified [RCV004880313]uncertain significance14569355145693551Humanname