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Pathways
Variants search result for All species
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12 records found for search term Lynx1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405816023CV3280954single nucleotide variantNM_177477.4(LYNX1):c.5C>T (p.Thr2Met)not specified [RCV004411008]uncertain significance8142775953142775953Humanname
407481110CV3449349single nucleotide variantNM_177477.4(LYNX1):c.8C>T (p.Pro3Leu)not specified [RCV004640331]uncertain significance8142775950142775950Humanname
329365179CV2440108single nucleotide variantNM_177477.4(LYNX1):c.73G>A (p.Val25Met)not specified [RCV004260572]uncertain significance8142775674142775674Humanname
401772576CV2719684single nucleotide variantNM_177477.4(LYNX1):c.70C>T (p.His24Tyr)not specified [RCV004329128]uncertain significance8142775677142775677Humanname
155922188CV2240645single nucleotide variantNM_177477.4(LYNX1):c.119C>T (p.Pro40Leu)not specified [RCV004599477]uncertain significance8142775628142775628Humanname
156251173CV2394282single nucleotide variantNM_177477.4(LYNX1):c.146C>T (p.Thr49Met)not specified [RCV004238512]uncertain significance8142775601142775601Humanname
329361849CV2448090single nucleotide variantNM_177477.4(LYNX1):c.110T>G (p.Met37Arg)not specified [RCV004263313]uncertain significance8142775637142775637Humanname
405816021CV3280952single nucleotide variantNM_177477.4(LYNX1):c.113G>A (p.Arg38His)not specified [RCV004411006]uncertain significance8142775634142775634Humanname
405816022CV3280953single nucleotide variantNM_177477.4(LYNX1):c.116G>C (p.Cys39Ser)not specified [RCV004411007]uncertain significance8142775631142775631Humanname
407481103CV3449348single nucleotide variantNM_177477.4(LYNX1):c.149G>A (p.Arg50His)not specified [RCV004640330]uncertain significance8142775598142775598Humanname
597644938CV3696898single nucleotide variantNM_177477.4(LYNX1):c.124A>G (p.Met42Val)not specified [RCV004942301]uncertain significance8142775623142775623Humanname
15158453CV758773single nucleotide variantNM_023946.5(LYNX1-SLURP2):c.360C>T (p.Ile120=)not provided [RCV000925073]benign8142764641142764641Humanname