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          • › C__97821361_10
          See other CHRNA3 GT Assays ›
          SNP ID:
          rs71534215
          Gene
          CHRNA3 CHRNB4
          Gene Name
          cholinergic receptor nicotinic alpha 3 subunit
          cholinergic receptor nicotinic beta 4 subunit
          Set Membership:
          -
          Chromosome Location:
          Chr.15: 78625289 - 78625289 on Build GRCh38
          Polymorphism:
          A/G, Transition substitution
          Context Sequence [VIC/FAM]:

          TAGCCACGTACTTCCAGTCCTCAAC[A/G]ACCTGCAGGCAGACAGAGGAGTTGG

          Assay ID C__97821361_10
          Size
          Availability Made To Order
          Catalog # 4351379
          Price
          Your Price
          Online offer:
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details



          Species:

          Human

          dbSNP Submissions:

          NA

          Phenotype:

          MIM: 118503 MIM: 118509

          Literature Links:

          CHRNA3 PubMed Links

          Allele Nomenclature:

          Minor Allele Frequency:

          1000Genome Applied Biosystems® HapMap
          Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
          EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
          SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
          AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
          EUR - Not Available
          AMR - Not Available
          CHRNA3 - cholinergic receptor nicotinic alpha 3 subunit
          There are no transcripts associated with this gene.
          CHRNB4 - cholinergic receptor nicotinic beta 4 subunit
          Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
          NM_000750.3 1201 Silent Mutation GTC,GTT V,V 447 NP_000741.1
          NM_001256567.1 1201 Missense Mutation TCG,TTG S,L 121 NP_001243496.1
          XM_011521186.2 1201 Silent Mutation GTC,GTT V,V 444 XP_011519488.1
          XM_011521187.2 1201 Silent Mutation GTC,GTT V,V 444 XP_011519489.1
          XM_011521190.2 1201 Silent Mutation GTC,GTT V,V 373 XP_011519492.1
          XM_011521191.2 1201 Silent Mutation GTC,GTT V,V 373 XP_011519493.1
          XM_011521192.2 1201 Silent Mutation GTC,GTT V,V 265 XP_011519494.1
          XM_017021885.1 1201 Silent Mutation GTC,GTT V,V 417 XP_016877374.1
          XM_017021886.1 1201 Intron XP_016877375.1
          XM_017021887.1 1201 Intron XP_016877376.1
          XM_017021888.1 1201 Intron XP_016877377.1
          XM_017021889.1 1201 Intron XP_016877378.1

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          More Information


          Panther Classification:

          Molecular Function -

          ligand-gated ion channel

          Gene Ontology Categories:

          Function(s) Process(es)

          action potential
          ion transport
          smooth muscle contraction
          regulation of smooth muscle contraction
          signal transduction
          synaptic transmission, cholinergic
          locomotory behavior
          response to nicotine
          behavioral response to nicotine
          regulation of neurotransmitter secretion
          protein heterooligomerization
          positive regulation of transmission of nerve impulse
          synaptic transmission involved in micturition
          cation transmembrane transport
          acetylcholine-activated cation-selective channel activity
          drug binding
          ligand-gated ion channel activity
          acetylcholine receptor activity
          acetylcholine binding
          protein heterodimerization activity

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