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          • › Search Tool
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          • › C_190355810_10
          See other GOSR2 GT Assays ›
          SNP ID:
          rs201863464
          Gene
          GOSR2 MIR5089 RPRML
          Gene Name
          golgi SNAP receptor complex member 2
          microRNA 5089
          reprimo like
          Set Membership:
          -
          Chromosome Location:
          Chr.17: 46978838 - 46978838 on Build GRCh38
          Polymorphism:
          A/G, Transition substitution
          Context Sequence [VIC/FAM]:

          CGACACCCACAGGCTGCGCTCGTCG[A/G]GCGCCAGCCCCGCGGGGACCCCGTC

          Assay ID C_190355810_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: 604027

          Literature Links:

          GOSR2 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)
          GOSR2 - golgi SNAP receptor complex member 2
          There are no transcripts associated with this gene.
          MIR5089 - microRNA 5089
          There are no transcripts associated with this gene.
          RPRML - reprimo like
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_203400.4 411 Missense Mutation CCC,CTC P,L 57 NP_981945.1

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          git-commit: ec8e7df5f8fec8d765bd419205f1b5046a016d37
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