Product Details

SNP ID

rs114760982

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:70957343 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACTTTGGTTCCATTATCTACTTGG[C/T]CTTCTAAATTTACGATGAAGGAGCA

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	4306	Intron			NP_001012523.1
NM_001244808.1	4306	UTR 3			NP_001231737.1
NM_001244810.1	4306	UTR 3			NP_001231739.1
NM_001244812.1	4306	UTR 3			NP_001231741.1
NM_001244813.1	4306	UTR 3			NP_001231742.1
NM_001244814.1	4306	UTR 3			NP_001231743.1
NM_001244815.1	4306	UTR 3			NP_001231744.1
NM_001244816.1	4306	UTR 3			NP_001231745.1
NM_032682.5	4306	UTR 3			NP_116071.2
XM_005264735.3	4306	Intron			XP_005264792.1
XM_005264736.3	4306	Intron			XP_005264793.1
XM_005264737.4	4306	Intron			XP_005264794.1
XM_005264742.3	4306	Intron			XP_005264799.1
XM_006713102.2	4306	UTR 3			XP_006713165.1
XM_006713103.2	4306	Intron			XP_006713166.1
XM_006713104.2	4306	Intron			XP_006713167.1
XM_011533584.2	4306	UTR 3			XP_011531886.1
XM_011533585.2	4306	UTR 3			XP_011531887.1
XM_011533588.2	4306	Intron			XP_011531890.1
XM_017006165.1	4306	UTR 3			XP_016861654.1
XM_017006166.1	4306	Intron			XP_016861655.1
XM_017006167.1	4306	Intron			XP_016861656.1
XM_017006168.1	4306	Intron			XP_016861657.1

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