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TCATGAATATACTTCTTTGCTAAAA[C/T]ACAGTTAATTGATTAGGCGAAGGTA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607686 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FIP1L1 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
|
FIP1L1 - factor interacting with PAPOLA and CPSF1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134937.1 | Intron | NP_001128409.1 | ||||
NM_001134938.1 | Intron | NP_001128410.1 | ||||
NM_030917.3 | Intron | NP_112179.2 | ||||
XM_005265769.4 | Intron | XP_005265826.1 | ||||
XM_005265773.4 | Intron | XP_005265830.1 | ||||
XM_005265774.4 | Intron | XP_005265831.1 | ||||
XM_005265778.4 | Intron | XP_005265835.1 | ||||
XM_005265779.4 | Intron | XP_005265836.1 | ||||
XM_005265781.4 | Intron | XP_005265838.1 | ||||
XM_005265782.4 | Intron | XP_005265839.1 | ||||
XM_017008662.1 | Intron | XP_016864151.1 | ||||
XM_017008663.1 | Intron | XP_016864152.1 | ||||
XM_017008664.1 | Intron | XP_016864153.1 | ||||
XM_017008665.1 | Intron | XP_016864154.1 | ||||
XM_017008666.1 | Intron | XP_016864155.1 | ||||
XM_017008667.1 | Intron | XP_016864156.1 | ||||
XM_017008668.1 | Intron | XP_016864157.1 | ||||
XM_017008669.1 | Intron | XP_016864158.1 | ||||
XM_017008670.1 | Intron | XP_016864159.1 | ||||
XM_017008671.1 | Intron | XP_016864160.1 |