Product Details

SNP ID

rs141204546

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:41338005 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATATCAATATTATCACTTATTTTG[C/T]TGATAAATGTTATTAAATTAAGAAC

Phenotype

MIM: 604531

Polymorphism

C/T, Transition 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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