Product Details

SNP ID

rs201090758

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:51154423 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCGTCTTTCAAGGCGAGGGGCCTC[C/T]TATCTCAAGCTGTGATACAGGGTAG

Phenotype

MIM: 156490

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NME1 PubMed Links

Gene Details

Gene

NME1

Gene Name

NME/NM23 nucleoside diphosphate kinase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000269.2	303	Intron			NP_000260.1
NM_198175.1	303	Missense Mutation	CCT,CTT	P17L	NP_937818.1

Gene

NME1-NME2

Gene Name

NME1-NME2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018136.2	303	Intron			NP_001018146.1

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