Product Details

SNP ID

rs201094833

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:32031024 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTACTTCTCCCTGAGCCTCCTGC[A/G]GATCATGGACGTGGTGAGTCCCGCC

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	232	Missense Mutation	CAG,CGG	Q61R	NP_000737.1
NM_001190455.2	232	Missense Mutation	CAG,CGG	Q90R	NP_001177384.1
XM_011521176.2	232	Intron			XP_011519478.2
XM_011521177.2	232	Intron			XP_011519479.1
XM_011521178.2	232	Missense Mutation	CAG,CGG	Q61R	XP_011519480.1
XM_017021882.1	232	UTR 5			XP_016877371.1
XM_017021883.1	232	UTR 5			XP_016877372.1
XM_017021884.1	232	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	232	Intron			XP_011520622.1

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