Product Details

SNP ID
rs201220646
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:37850388 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTCCACTTTGCAGACAGTCATCA[A/G]TAATCAAAGCCTGTGGGATGAGATG
Phenotype
MIM: 607421
Polymorphism
A/G, 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_016616.4 416 Missense Mutation AAT,AGT N15S NP_057700.3

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