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SNP ID:
rs1786062
Gene
CELF4
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.18: 37250834 - 37250834 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

GCTGGGAAGCCTGACAGCACCATTC[A/G]TTAAAATACTGTCTAAATGAAAATT

Assay ID C___7462615_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 612679

Literature Links:

 CELF4 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.07)
(0.93)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
T (0.00)
(1.00)
African American - Not Available YRI (Yoruba)
T (0.24)
(0.76)
SAS
T (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
T (0.25)
(0.75)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
T (0.00)
(1.00)
AMR
T (0.03)
(0.97)
CELF4 - CUGBP, Elav-like family member 4
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001025087.1 Intron NP_001020258.1
NM_001025088.1 Intron NP_001020259.1
NM_001025089.1 Intron NP_001020260.1
NM_020180.3 Intron NP_064565.1
XM_005258308.3 Intron XP_005258365.1
XM_011526079.2 Intron XP_011524381.1
XM_011526081.2 Intron XP_011524383.1
XM_011526083.2 Intron XP_011524385.1
XM_011526084.2 Intron XP_011524386.1
XM_011526085.2 Intron XP_011524387.1
XM_011526086.2 Intron XP_011524388.1
XM_011526087.2 Intron XP_011524389.1
XM_011526090.2 Intron XP_011524392.1
XM_011526091.2 Intron XP_011524393.1
XM_011526092.2 Intron XP_011524394.1
XM_017025840.1 Intron XP_016881329.1
XM_017025841.1 Intron XP_016881330.1
XM_017025842.1 Intron XP_016881331.1
XM_017025843.1 Intron XP_016881332.1
XM_017025844.1 Intron XP_016881333.1
XM_017025845.1 Intron XP_016881334.1
XM_017025846.1 Intron XP_016881335.1
XM_017025847.1 Intron XP_016881336.1
XM_017025848.1 Intron XP_016881337.1
XM_017025849.1 Intron XP_016881338.1
XM_017025850.1 Intron XP_016881339.1
XM_017025851.1 Intron XP_016881340.1
XM_017025852.1 Intron XP_016881341.1
XM_017025853.1 Intron XP_016881342.1
XM_017025854.1 Intron XP_016881343.1
XM_017025855.1 Intron XP_016881344.1
XM_017025856.1 Intron XP_016881345.1
XM_017025857.1 Intron XP_016881346.1
XM_017025858.1 Intron XP_016881347.1
XM_017025859.1 Intron XP_016881348.1
XM_017025860.1 Intron XP_016881349.1
XM_017025861.1 Intron XP_016881350.1
XM_017025862.1 Intron XP_016881351.1
XM_017025863.1 Intron XP_016881352.1
XM_017025864.1 Intron XP_016881353.1
XM_017025865.1 Intron XP_016881354.1
XM_017025866.1 Intron XP_016881355.1
XM_017025867.1 Intron XP_016881356.1
XM_017025868.1 Intron XP_016881357.1
XM_017025869.1 Intron XP_016881358.1
XM_017025870.1 Intron XP_016881359.1
XM_017025871.1 Intron XP_016881360.1
XM_017025872.1 Intron XP_016881361.1

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