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9 records found for search term Pfn4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407487064CV3466850single nucleotide variantNM_199346.3(PFN4):c.64G>T (p.Ala22Ser)not specified [RCV004655777]uncertain significance22412247224122472Humanname
155967444CV2261161single nucleotide variantNM_199346.3(PFN4):c.268G>A (p.Val90Met)not specified [RCV004128054]uncertain significance22411967024119670Humanname
405746519CV3368576single nucleotide variantNM_199346.3(PFN4):c.114C>A (p.Phe38Leu)not specified [RCV004498474]uncertain significance22412242224122422Humanname
405746527CV3368577single nucleotide variantNM_199346.3(PFN4):c.223C>T (p.Arg75Trp)not specified [RCV004498475]uncertain significance22412119524121195Humanname
597685326CV3575859single nucleotide variantNM_199346.3(PFN4):c.128G>T (p.Ser43Ile)not specified [RCV004842254]uncertain significance22412129024121290Humanname
597685338CV3575860single nucleotide variantNM_199346.3(PFN4):c.179G>T (p.Arg60Leu)not specified [RCV004842255]uncertain significance22412123924121239Humanname
598262218CV3999760single nucleotide variantNM_199346.3(PFN4):c.245A>G (p.Tyr82Cys)not specified [RCV005387045]uncertain significance22412117324121173Humanname
401858461CV2758817single nucleotide variantNM_199346.3(PFN4):c.375A>C (p.Arg125Ser)not specified [RCV004337867]uncertain significance22411559824115598Humanname
405746534CV3368578single nucleotide variantNM_199346.3(PFN4):c.319G>A (p.Gly107Ser)not specified [RCV004498476]likely benign22411961924119619Humanname