Product Details

SNP ID
rs199746651
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:32030905 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGTCTTCTCTCCTTAAGTGTCCCT[A/G]CAAGGCGAGTTCCAGAGGAAGCTTT
Phenotype
MIM: 118511
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CHRNA7 PubMed Links

Gene Details

Gene
CHRNA7
Gene Name
cholinergic receptor nicotinic alpha 7 subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000746.5 113 Silent Mutation CTA,CTG L21L NP_000737.1
NM_001190455.2 113 Silent Mutation CTA,CTG L50L NP_001177384.1
XM_011521176.2 113 Intron XP_011519478.2
XM_011521177.2 113 Intron XP_011519479.1
XM_011521178.2 113 Silent Mutation CTA,CTG L21L XP_011519480.1
XM_017021882.1 113 UTR 5 XP_016877371.1
XM_017021883.1 113 UTR 5 XP_016877372.1
XM_017021884.1 113 UTR 5 XP_016877373.1
Gene
LOC105370940
Gene Name
uncharacterized LOC105370940
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_011522320.2 113 Intron XP_011520622.1

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