Product Details

SNP ID

rs6504957

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46715807 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTATTTAATCTTCAAATTGTTGAAG[C/G]CTTTCAAGGTAGAGTTTCAGATGAG

Phenotype

MIM: 601633

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NSF PubMed Links

Gene Details

Gene

NSF

Gene Name

N-ethylmaleimide sensitive factor, vesicle fusing ATPase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006178.3		Intron			NP_006169.2

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