Product Details

SNP ID

rs7811628

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:114099906 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGGGATTCATTTAACTGAAGATTT[C/T]AGCTGGTCCTGCCAGCAAATCAAAA

Phenotype

MIM: 605317

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXP2 PubMed Links

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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