Product Details

SNP ID
rs187837692
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:232526668 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCCTCACACTCTCCAACCTCAT[C/T]TCCCTGGTGAGAGGCCCTCCGGTGC
Phenotype
MIM: 100720 MIM: 613858
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CHRND PubMed Links

Gene Details

Gene
CHRND
Gene Name
cholinergic receptor nicotinic delta subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000751.2 220 Silent Mutation ATC,ATT I64I NP_000742.1
NM_001256657.1 220 Silent Mutation ATC,ATT I64I NP_001243586.1
NM_001311195.1 220 UTR 5 NP_001298124.1
NM_001311196.1 220 UTR 5 NP_001298125.1
XM_011510524.2 220 UTR 5 XP_011508826.1
Gene
PRSS56
Gene Name
protease, serine 56
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195129.1 220 Intron NP_001182058.1

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