Product Details

SNP ID
rs200032652
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:63346862 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCACGTACTTCCAGTCCTCCTTC[A/C]CCTGCAAGCACAGACGCCGTCACTC
Phenotype
MIM: 118504
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CHRNA4 PubMed Links

Gene Details

Gene
CHRNA4
Gene Name
cholinergic receptor nicotinic alpha 4 subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000744.6 1991 Missense Mutation GGG,GTG G587V NP_000735.1
NM_001256573.1 1991 Missense Mutation GGG,GTG G411V NP_001243502.1
XM_011528524.1 1991 Missense Mutation GGG,GTG G516V XP_011526826.1
XM_017027624.1 1991 Missense Mutation GGG,GTG G506V XP_016883113.1
XM_017027625.1 1991 Missense Mutation GGG,GTG G411V XP_016883114.1

View Full Product Details