Product Details

SNP ID

rs1051168

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:84657289 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGCTGGTCCCTCAGGGAGGTGTGGG[G/T]AGCTGTCCCCAATGGGGATGGGCTG

Phenotype

MIM: 162340 MIM: 616144

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

NMB PubMed Links

Gene Details

Gene

NMB

Gene Name

neuromedin B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021077.3	636	Missense Mutation	ACC,CCC	T73P	NP_066563.2
NM_205858.1	636	Missense Mutation	ACC,CCC	T73P	NP_995580.1
XM_017022239.1	636	Intron			XP_016877728.1

Gene

WDR73

Gene Name

WD repeat domain 73

There are no transcripts associated with this gene.

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