Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAAGGCGGCTTTAGTGGCAGCATG[A/G]AGCGCACCCCGACTGCCGAGGAACG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610966 MIM: 610937 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FTO PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
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
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FTO - fat mass and obesity associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080432.2 | 190 | Missense Mutation | AAG,GAG | K,E 2 | NP_001073901.1 | |
XM_011523313.2 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_011521615.1 | |
XM_011523314.2 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_011521616.1 | |
XM_011523315.2 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_011521617.1 | |
XM_011523316.2 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_011521618.1 | |
XM_017023654.1 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_016879143.1 | |
XM_017023655.1 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_016879144.1 | |
XM_017023656.1 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_016879145.1 | |
XM_017023657.1 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_016879146.1 | |
XM_017023658.1 | 190 | Missense Mutation | AAG,GAG | K,E 2 | XP_016879147.1 |
RPGRIP1L - RPGRIP1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005255867.1 | 190 | Intron | XP_005255924.1 | |||
XM_005255868.1 | 190 | Intron | XP_005255925.1 | |||
XM_011522970.1 | 190 | Intron | XP_011521272.1 | |||
XM_011522971.2 | 190 | Intron | XP_011521273.1 | |||
XM_011522973.2 | 190 | Intron | XP_011521275.1 | |||
XM_017023094.1 | 190 | Intron | XP_016878583.1 | |||
XM_017023095.1 | 190 | Intron | XP_016878584.1 | |||
XM_017023096.1 | 190 | Intron | XP_016878585.1 | |||
XM_017023097.1 | 190 | Intron | XP_016878586.1 | |||
XM_017023098.1 | 190 | Intron | XP_016878587.1 | |||
XM_017023099.1 | 190 | Intron | XP_016878588.1 | |||
XM_017023100.1 | 190 | Intron | XP_016878589.1 |