Product Details

SNP ID

rs200758390

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:37850632 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATAAATATCATCATCTTCTAGTGA[C/T]TGATGTTTACCAAGCCTGGTGTGGA

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	467	Missense Mutation	ACT,ATT	T32I	NP_057700.3

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