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TGGGAAGGTCACATTTCATGGAGAA[C/T]CTAAAGGAGGTGAGGAGTGAACATA
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609073 | ||||||||||||||||||||||||||
Literature Links: |
FBXW8 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
FBXW8 - F-box and WD repeat domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012174.1 | Intron | NP_036306.1 | ||||
NM_153348.2 | Intron | NP_699179.2 | ||||
XM_005253867.2 | Intron | XP_005253924.1 | ||||
XM_005253868.3 | Intron | XP_005253925.1 | ||||
XM_017019175.1 | Intron | XP_016874664.1 | ||||
XM_017019176.1 | Intron | XP_016874665.1 | ||||
XM_017019177.1 | Intron | XP_016874666.1 | ||||
XM_017019178.1 | Intron | XP_016874667.1 |