Product Details

SNP ID

rs56270258

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:21511115 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGTTGGGGAACCGCGCCGAATAG[C/T]TGAGCTCCAAGTTCGGGGCTGAAGG

Phenotype

MIM: 604612

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NKX2-2 PubMed Links

Additional Information

For this assay, SNP(s) [rs141691214] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NKX2-2

Gene Name

NK2 homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002509.3	1644	UTR 3			NP_002500.1
XM_006723566.3	1644	UTR 3			XP_006723629.1

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