Product Details

SNP ID
rs34166421
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:136873301 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCTGGCCTATGTGGTGGAGGTGGT[A/G]TGTGGGGAAAGAGATGCAAGTCACC
Phenotype
MIM: 118493
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CHRM2 PubMed Links

Gene Details

Gene
CHRM2
Gene Name
cholinergic receptor muscarinic 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000739.2 Intron NP_000730.1
NM_001006626.1 Intron NP_001006627.1
NM_001006627.1 Intron NP_001006628.1
NM_001006628.1 Intron NP_001006629.1
NM_001006629.1 Intron NP_001006630.1
NM_001006630.1 Intron NP_001006631.1
NM_001006631.1 Intron NP_001006632.1
NM_001006632.1 Intron NP_001006633.1
XM_011515769.2 Intron XP_011514071.1

View Full Product Details