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Variants search result for Homo sapiens
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11 records found for search term Ap3s1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8580268CV114698single nucleotide variantNM_001284.2(AP3S1):c.70-6112C>ALung cancer [RCV000095221]uncertain significance5115860558115860558Humanname
329396173CV2451937single nucleotide variantNM_001284.4(AP3S1):c.17T>C (p.Leu6Pro)not specified [RCV004276603]uncertain significance5115842054115842054Humanname
598203697CV3990483single nucleotide variantNM_001284.4(AP3S1):c.71G>T (p.Ser24Ile)not specified [RCV005376461]uncertain significance5115866671115866671Humanname
598158681CV3990494single nucleotide variantNM_001284.4(AP3S1):c.61C>A (p.Gln21Lys)not specified [RCV005389974]uncertain significance5115842098115842098Humanname
401760776CV2695156single nucleotide variantNM_001284.4(AP3S1):c.175T>A (p.Ser59Thr)not specified [RCV004303306]uncertain significance5115870030115870030Humanname
407498680CV3465648single nucleotide variantNM_001284.4(AP3S1):c.143A>G (p.Asn48Ser)not specified [RCV004644091]uncertain significance5115866743115866743Humanname
597639250CV3565587single nucleotide variantNM_001284.4(AP3S1):c.218T>C (p.Phe73Ser)not specified [RCV004831912]uncertain significance5115870073115870073Humanname
407498694CV3465654single nucleotide variantNM_001284.4(AP3S1):c.426T>G (p.Asp142Glu)not specified [RCV004644095]uncertain significance5115902965115902965Humanname
597639205CV3565567single nucleotide variantNM_001284.4(AP3S1):c.423T>G (p.Ile141Met)not specified [RCV004831903]uncertain significance5115902962115902962Humanname
597639210CV3565578single nucleotide variantNM_001284.4(AP3S1):c.511C>A (p.Pro171Thr)not specified [RCV004831904]uncertain significance5115913419115913419Humanname
15164266CV698737single nucleotide variantNM_001284.4(AP3S1):c.473C>T (p.Pro158Leu)not provided [RCV000948298]benign5115913381115913381Humanname