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SNP ID:
rs9939609
Gene
FTO
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.16: 53786615 - 53786615 on Build GRCh38
Polymorphism:
A/T, Transversion substitution
Context Sequence [VIC/FAM]:

GGTTCCTTGCGACTGCTGTGAATTT[A/T]GTGATGCACTTGGATAGTCTCTGTT

Assay ID C__30090620_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 610966

Literature Links:

 FTO PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.34)
(0.66)
Caucasian - Not Available CEPH (CEU)
A (0.46)
(0.54)
EAS
A (0.17)
(0.83)
African American - Not Available YRI (Yoruba)
T (0.49)
(0.51)
SAS
A (0.29)
(0.71)
Chinese - Not Available JPT (Japanese)
T (0.19)
(0.81)
AFR
T (0.49)
(0.51)
Japanese - Not Available CHB (Han Chinese)
A (0.12)
(0.88)
EUR
T (0.41)
(0.59)
AMR
A (0.26)
(0.74)
FTO - fat mass and obesity associated
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001080432.2 Intron NP_001073901.1
XM_011523313.2 Intron XP_011521615.1
XM_011523314.2 Intron XP_011521616.1
XM_011523315.2 Intron XP_011521617.1
XM_011523316.2 Intron XP_011521618.1
XM_017023654.1 Intron XP_016879143.1
XM_017023655.1 Intron XP_016879144.1
XM_017023656.1 Intron XP_016879145.1
XM_017023657.1 Intron XP_016879146.1
XM_017023658.1 Intron XP_016879147.1

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