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SNP ID:
rs9878602
Gene
FOXP1
Gene Name
Set Membership:
-
Chromosome Location:
Chr.3: 71486187 - 71486187 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

AGGTGACTTATGCACTAACCTTCTC[G/T]CTTCTCAACATTAAAACCAGAATAA

Assay ID C____203981_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 605515

Literature Links:

 FOXP1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.31)
(0.69)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
FOXP1 - forkhead box P1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid 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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