Product Details

SNP ID
rs74639445
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:70960762 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGGACTGCCCTTGAAGACAGGAA[C/T]CTTCAGAATCAATTGACTCTAAAAT
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 Intron NP_001012523.1
NM_001244808.1 Intron NP_001231737.1
NM_001244810.1 Intron NP_001231739.1
NM_001244812.1 Intron NP_001231741.1
NM_001244813.1 Intron NP_001231742.1
NM_001244814.1 Intron NP_001231743.1
NM_001244815.1 Intron NP_001231744.1
NM_001244816.1 Intron NP_001231745.1
NM_032682.5 Intron NP_116071.2
XM_005264735.3 Intron XP_005264792.1
XM_005264736.3 Intron XP_005264793.1
XM_005264737.4 Intron XP_005264794.1
XM_005264742.3 Intron XP_005264799.1
XM_006713102.2 Intron XP_006713165.1
XM_006713103.2 Intron XP_006713166.1
XM_006713104.2 Intron XP_006713167.1
XM_011533584.2 Intron XP_011531886.1
XM_011533585.2 Intron XP_011531887.1
XM_011533588.2 Intron XP_011531890.1
XM_017006165.1 Intron XP_016861654.1
XM_017006166.1 Intron XP_016861655.1
XM_017006167.1 Intron XP_016861656.1
XM_017006168.1 Intron XP_016861657.1

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