Product Details

SNP ID

rs3804278

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:41337716 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATAGAAGAAATTTTAAAGCAATTCC[G/T]ACAAGCTCAACAGTTTTATATTTAA

Phenotype

MIM: 604531

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

NCR2 PubMed Links

Gene Details

Gene

NCR2

Gene Name

natural cytotoxicity triggering receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199509.1		Intron			NP_001186438.1
NM_001199510.1		Intron			NP_001186439.1
NM_004828.3		Intron			NP_004819.2
XM_017011500.1		Intron			XP_016866989.1

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