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AGGATGGGAGATTAACACCCAAAGC[A/G]CAAGGGTGGAAATAAATAGAGGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609071 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXW2 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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FBXW2 - F-box and WD repeat domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012164.3 | 7836 | UTR 3 | NP_036296.2 | |||
XM_005251910.3 | 7836 | Intron | XP_005251967.1 | |||
XM_005251913.2 | 7836 | Intron | XP_005251970.1 | |||
XM_006717049.3 | 7836 | Intron | XP_006717112.1 | |||
XM_006717051.2 | 7836 | Intron | XP_006717114.1 | |||
XM_011518518.1 | 7836 | Intron | XP_011516820.1 | |||
XM_017014615.1 | 7836 | Intron | XP_016870104.1 | |||
XM_017014616.1 | 7836 | Intron | XP_016870105.1 | |||
XM_017014617.1 | 7836 | Intron | XP_016870106.1 |