Product Details

SNP ID
rs7662646
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:55603424 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAAAAAAAAATTGCCTAGATCAGAA[G/T]TCAGAAAACTATTTTGTACTTTCTC
Phenotype
MIM: 605103
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
NMU PubMed Links

Gene Details

Gene
NMU
Gene Name
neuromedin U
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001292045.1 Intron NP_001278974.1
NM_001292046.1 Intron NP_001278975.1
NM_006681.3 Intron NP_006672.1
XM_011534367.2 Intron XP_011532669.1
XM_011534368.2 Intron XP_011532670.1

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