Product Details

SNP ID: rs2722372
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.7:37850665 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TACCAAGCCTGGTGTGGACCTTGCA[A/G]AGCAATGCAACCTTTATTCAGAAAA
Phenotype: MIM: 607421
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NME8 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016616.4	500	Missense Mutation	AAA,AGA	K43R	NP_057700.3