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Variants search result for Homo sapiens
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19 records found for search term Marcksl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15176519CV743744single nucleotide variantNM_023009.7(MARCKSL1):c.88-8C>Tnot provided [RCV000906448]benign13233510532335105Humanname
15102855CV761875single nucleotide variantNM_023009.7(MARCKSL1):c.96C>A (p.Gly32=)not provided [RCV000937074]likely benign13233508932335089Humanname
15171380CV718918single nucleotide variantNM_023009.7(MARCKSL1):c.546G>A (p.Pro182=)not provided [RCV000883643]benign13233463932334639Humanname
329400807CV2448917single nucleotide variantNM_023009.7(MARCKSL1):c.209C>G (p.Pro70Arg)not specified [RCV004261956]uncertain significance13233497632334976Humanname
407494764CV3456869single nucleotide variantNM_023009.7(MARCKSL1):c.137G>A (p.Gly46Glu)not specified [RCV004643065]uncertain significance13233504832335048Humanname
597636348CV3697568single nucleotide variantNM_023009.7(MARCKSL1):c.188A>T (p.Asp63Val)not specified [RCV004940765]uncertain significance13233499732334997Humanname
598198761CV3985466single nucleotide variantNM_023009.7(MARCKSL1):c.263A>G (p.Lys88Arg)not specified [RCV005375601]uncertain significance13233492232334922Humanname
598198778CV3985468single nucleotide variantNM_023009.7(MARCKSL1):c.193A>G (p.Ile65Val)not specified [RCV005375603]uncertain significance13233499232334992Humanname
155913631CV2245910single nucleotide variantNM_023009.7(MARCKSL1):c.466G>A (p.Ala156Thr)not specified [RCV004111748]uncertain significance13233471932334719Humanname
156018772CV2272380single nucleotide variantNM_023009.7(MARCKSL1):c.394G>C (p.Gly132Arg)not specified [RCV004133305]uncertain significance13233479132334791Humanname
156051781CV2386423single nucleotide variantNM_023009.7(MARCKSL1):c.347C>A (p.Ser116Tyr)not specified [RCV004228750]uncertain significance13233483832334838Humanname
401760219CV2718759single nucleotide variantNM_023009.7(MARCKSL1):c.356C>T (p.Ser119Phe)not specified [RCV004328512]uncertain significance13233482932334829Humanname
401885842CV2774567single nucleotide variantNM_023009.7(MARCKSL1):c.472G>T (p.Gly158Trp)not specified [RCV004350047]uncertain significance13233471332334713Humanname
401893002CV2791852single nucleotide variantNM_023009.7(MARCKSL1):c.334G>A (p.Gly112Ser)not specified [RCV004359296]uncertain significance13233485132334851Humanname
405658252CV3281560single nucleotide variantNM_023009.7(MARCKSL1):c.335G>A (p.Gly112Asp)not specified [RCV004416381]uncertain significance13233485032334850Humanname
405658254CV3281561single nucleotide variantNM_023009.7(MARCKSL1):c.426A>C (p.Glu142Asp)not specified [RCV004416382]uncertain significance13233475932334759Humanname
407494768CV3456870single nucleotide variantNM_023009.7(MARCKSL1):c.478G>C (p.Glu160Gln)not specified [RCV004643066]uncertain significance13233470732334707Humanname
597636342CV3697567single nucleotide variantNM_023009.7(MARCKSL1):c.422A>G (p.Gln141Arg)not specified [RCV004940764]uncertain significance13233476332334763Humanname
598198771CV3985467single nucleotide variantNM_023009.7(MARCKSL1):c.530C>A (p.Ser177Tyr)not specified [RCV005375602]uncertain significance13233465532334655Humanname