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SNP ID

rs16892524

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:119417239 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTAGACAAGAATCTAAGCAAAGGGG[C/G]AGCCACGCAGAGTTAAGGGCCAGTG

Phenotype

MIM: 164958

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NOV PubMed Links

Gene Details

Gene

NOV

Gene Name

nephroblastoma overexpressed

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002514.3		Intron			NP_002505.1

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