Product Details

SNP ID

rs989655

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:37252711 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGCACCCAGTTCTCCTCCATGAGG[G/T]TATTCTCTCCATCTCCAGCTTTTCG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

NWD2 PubMed Links

Gene Details

Gene

NWD2

Gene Name

NACHT and WD repeat domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144990.1		Intron			NP_001138462.1

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