Product Details

SNP ID
rs150510076
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:142075865 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGTAGGTAAAGAGCAAATGGGTTG[A/G]CACAAGAATTGCCAAAACTGAGAAC
Phenotype
MIM: 162341
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NMBR PubMed Links

Gene Details

Gene
NMBR
Gene Name
neuromedin B receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324307.1 633 Missense Mutation GCC,GTC A171V NP_001311236.1
NM_001324308.1 633 Missense Mutation GCC,GTC A171V NP_001311237.1
NM_002511.3 633 Missense Mutation GCC,GTC A319V NP_002502.2
XM_011535846.1 633 Missense Mutation GCC,GTC A212V XP_011534148.1
XM_017010901.1 633 Missense Mutation GCC,GTC A230V XP_016866390.1
XM_017010902.1 633 Missense Mutation GCC,GTC A171V XP_016866391.1

View Full Product Details