Product Details

SNP ID

rs2598041

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:37852190 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTTAAAAAATGTCTTTATATAGAT[G/T]TTATTTTTAGAGCAGTTTTAGGCTC

Phenotype

MIM: 607421

Polymorphism

G/T, Transversion 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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