Product Details

SNP ID

rs1470719

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:37851263 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTAATTAGAATTTCGTTGTCCAACA[C/T]GGTAGCTACTAGGCATAAGTGACTA

Phenotype

MIM: 607421

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NME8 PubMed Links

Gene Details

Gene

NME8

Gene Name

NME/NM23 family member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016616.4		Intron			NP_057700.3

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