Product Details

SNP ID
rs13082259
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:70957908 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTGCATTCAAACAGTTTAATGCC[A/C]CCAAGTAGGTCTGAACTAATGTATA
Phenotype
MIM: 605515
Polymorphism
A/C, Transversion 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 3741 Intron NP_001012523.1
NM_001244808.1 3741 UTR 3 NP_001231737.1
NM_001244810.1 3741 UTR 3 NP_001231739.1
NM_001244812.1 3741 UTR 3 NP_001231741.1
NM_001244813.1 3741 UTR 3 NP_001231742.1
NM_001244814.1 3741 UTR 3 NP_001231743.1
NM_001244815.1 3741 UTR 3 NP_001231744.1
NM_001244816.1 3741 UTR 3 NP_001231745.1
NM_032682.5 3741 UTR 3 NP_116071.2
XM_005264735.3 3741 Intron XP_005264792.1
XM_005264736.3 3741 Intron XP_005264793.1
XM_005264737.4 3741 Intron XP_005264794.1
XM_005264742.3 3741 Intron XP_005264799.1
XM_006713102.2 3741 UTR 3 XP_006713165.1
XM_006713103.2 3741 Intron XP_006713166.1
XM_006713104.2 3741 Intron XP_006713167.1
XM_011533584.2 3741 UTR 3 XP_011531886.1
XM_011533585.2 3741 UTR 3 XP_011531887.1
XM_011533588.2 3741 Intron XP_011531890.1
XM_017006165.1 3741 UTR 3 XP_016861654.1
XM_017006166.1 3741 Intron XP_016861655.1
XM_017006167.1 3741 Intron XP_016861656.1
XM_017006168.1 3741 Intron XP_016861657.1

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