Product Details

SNP ID

rs15187

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:70956827 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTATACAGAAAGCAGAGTGAAGCTT[C/T]AAAAGTAACTGCCAGAGAAGTTTTT

Phenotype

MIM: 605515

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FOXP1 PubMed Links

Gene Details

Gene

FOXP1

Gene Name

forkhead box P1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012505.1	4822	Intron			NP_001012523.1
NM_001244808.1	4822	UTR 3			NP_001231737.1
NM_001244810.1	4822	UTR 3			NP_001231739.1
NM_001244812.1	4822	UTR 3			NP_001231741.1
NM_001244813.1	4822	UTR 3			NP_001231742.1
NM_001244814.1	4822	UTR 3			NP_001231743.1
NM_001244815.1	4822	UTR 3			NP_001231744.1
NM_001244816.1	4822	UTR 3			NP_001231745.1
NM_032682.5	4822	UTR 3			NP_116071.2
XM_005264735.3	4822	Intron			XP_005264792.1
XM_005264736.3	4822	Intron			XP_005264793.1
XM_005264737.4	4822	Intron			XP_005264794.1
XM_005264742.3	4822	Intron			XP_005264799.1
XM_006713102.2	4822	UTR 3			XP_006713165.1
XM_006713103.2	4822	Intron			XP_006713166.1
XM_006713104.2	4822	Intron			XP_006713167.1
XM_011533584.2	4822	UTR 3			XP_011531886.1
XM_011533585.2	4822	UTR 3			XP_011531887.1
XM_011533588.2	4822	Intron			XP_011531890.1
XM_017006165.1	4822	UTR 3			XP_016861654.1
XM_017006166.1	4822	Intron			XP_016861655.1
XM_017006167.1	4822	Intron			XP_016861656.1
XM_017006168.1	4822	Intron			XP_016861657.1

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