Product Details

SNP ID

rs10277056

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:114104527 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGATGAAAATTTAAGAAAAATGT[A/G]ATTGAAAAACTATTGATATGTACAT

Phenotype

MIM: 605317

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FOXP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs74872336] are located under a probe 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

FOXP2

Gene Name

forkhead box P2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172766.2		Intron			NP_001166237.1
NM_001172767.2		Intron			NP_001166238.1
NM_014491.3		Intron			NP_055306.1
NM_148898.3		Intron			NP_683696.2
NM_148899.3		Intron			NP_683697.2
NM_148900.3		Intron			NP_683698.2
XM_017012801.1		Intron			XP_016868290.1

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