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ACATTAGGTACTACTAGGTTCTCTA[C/T]GAGTAGCATACAACTTTTGGGGCAC
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 | |||
---|---|---|---|---|---|
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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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 |