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          • › C_174796260_10
          See other ELAVL2 GT Assays ›
          SNP ID:
          rs142761114
          Gene
          ELAVL2
          Gene Name
          ELAV like neuron-specific RNA binding protein 2
          Set Membership:
          -
          Chromosome Location:
          Chr.9: 23692779 - 23692779 on Build GRCh38
          Polymorphism:
          A/G, Transition substitution
          Context Sequence [VIC/FAM]:

          TTTGCCACAGGATACTCTCATCTGC[A/G]TCAGGAGCCAGGTTGTACACAAATA

          Assay ID C_174796260_10
          Size
          Availability Made To Order
          Catalog # 4351379
          Price
          Your Price
          Online offer:
          Check your price ›
          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details



          Species:

          Human

          dbSNP Submissions:

          NA

          Phenotype:

          MIM: 601673

          Literature Links:

          ELAVL2 PubMed Links

          Allele Nomenclature:

          Minor Allele Frequency:

          1000Genome Applied Biosystems® HapMap
          Global
          A (0.00)
          (1.00)
          Caucasian - Not Available CEPH (CEU) - Not Available
          EAS
          A (0.00)
          (1.00)
          African American - Not Available YRI (Yoruba) - Not Available
          SAS
          A (0.00)
          (1.00)
          Chinese - Not Available CHB (Han Chinese) - Not Available
          AFR
          A (0.00)
          (1.00)
          Japanese - Not Available JPT (Japanese) - Not Available
          EUR
          A (0.00)
          (1.00)
          AMR
          A (0.00)
          (1.00)
          ELAVL2 - ELAV like neuron-specific RNA binding protein 2
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_001171195.1 1373 Silent Mutation GAC,GAT D,D 273 NP_001164666.1
          NM_001171197.1 1373 Silent Mutation GAC,GAT D,D 273 NP_001164668.1
          NM_004432.3 1373 Silent Mutation GAC,GAT D,D 286 NP_004423.2
          XM_005251393.3 1373 Silent Mutation GAC,GAT D,D 287 XP_005251450.1
          XM_005251394.3 1373 Silent Mutation GAC,GAT D,D 287 XP_005251451.1
          XM_005251395.3 1373 Silent Mutation GAC,GAT D,D 287 XP_005251452.1
          XM_006716734.3 1373 Silent Mutation GAC,GAT D,D 316 XP_006716797.1
          XM_006716735.3 1373 Silent Mutation GAC,GAT D,D 316 XP_006716798.1
          XM_006716736.3 1373 Silent Mutation GAC,GAT D,D 287 XP_006716799.1
          XM_011517774.2 1373 Silent Mutation GAC,GAT D,D 315 XP_011516076.1
          XM_011517776.2 1373 Silent Mutation GAC,GAT D,D 303 XP_011516078.1
          XM_011517777.2 1373 Silent Mutation GAC,GAT D,D 302 XP_011516079.1
          XM_011517778.2 1373 Silent Mutation GAC,GAT D,D 319 XP_011516080.2
          XM_011517779.2 1373 Silent Mutation GAC,GAT D,D 316 XP_011516081.1
          XM_011517780.2 1373 Silent Mutation GAC,GAT D,D 316 XP_011516082.1
          XM_011517783.2 1373 Silent Mutation GAC,GAT D,D 301 XP_011516085.1
          XM_011517784.2 1373 Silent Mutation GAC,GAT D,D 287 XP_011516086.1
          XM_011517785.2 1373 Silent Mutation GAC,GAT D,D 287 XP_011516087.1
          XM_011517786.2 1373 Silent Mutation GAC,GAT D,D 287 XP_011516088.1
          XM_017014408.1 1373 Silent Mutation GAC,GAT D,D 315 XP_016869897.1
          XM_017014409.1 1373 Silent Mutation GAC,GAT D,D 315 XP_016869898.1
          XM_017014410.1 1373 Silent Mutation GAC,GAT D,D 315 XP_016869899.1
          XM_017014411.1 1373 Silent Mutation GAC,GAT D,D 315 XP_016869900.1
          XM_017014412.1 1373 Silent Mutation GAC,GAT D,D 315 XP_016869901.1
          XM_017014413.1 1373 Silent Mutation GAC,GAT D,D 314 XP_016869902.1
          XM_017014414.1 1373 Silent Mutation GAC,GAT D,D 314 XP_016869903.1
          XM_017014415.1 1373 Silent Mutation GAC,GAT D,D 303 XP_016869904.1
          XM_017014416.1 1373 Silent Mutation GAC,GAT D,D 302 XP_016869905.1
          XM_017014417.1 1373 Silent Mutation GAC,GAT D,D 300 XP_016869906.1
          XM_017014418.1 1373 Silent Mutation GAC,GAT D,D 287 XP_016869907.1
          XM_017014419.1 1373 Silent Mutation GAC,GAT D,D 286 XP_016869908.1
          XM_017014420.1 1373 Silent Mutation GAC,GAT D,D 286 XP_016869909.1
          XM_017014421.1 1373 Silent Mutation GAC,GAT D,D 286 XP_016869910.1
          XM_017014422.1 1373 Silent Mutation GAC,GAT D,D 286 XP_016869911.1
          XM_017014423.1 1373 Silent Mutation GAC,GAT D,D 286 XP_016869912.1
          XM_017014424.1 1373 Silent Mutation GAC,GAT D,D 273 XP_016869913.1
          XM_017014425.1 1373 Silent Mutation GAC,GAT D,D 273 XP_016869914.1
          XM_017014426.1 1373 Silent Mutation GAC,GAT D,D 152 XP_016869915.1

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          More Information


          Panther Classification:

          Molecular Function -

          translation initiation factor

          Gene Ontology Categories:

          Function(s) Process(es)

          mRNA splicing, via spliceosome
          regulation of transcription, DNA-templated
          nucleotide binding
          mRNA 3'-UTR binding
          protein binding
          poly(A) RNA binding

          Back To Top

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