Product Details

SNP ID

rs13123248

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55602349 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTAGGCCCAGCAAAGCGAACACT[C/T]TCCTGCAATTGCATTTCTATTCATC

Phenotype

MIM: 605103

Polymorphism

C/T, Transition 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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