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GGTGCAGGGTATTTAGTCTAAAAAT[C/T]TACGTATAGTTTGTGCACTAGGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608533 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXO38 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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FBXO38 - F-box protein 38 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271723.1 | Intron | NP_001258652.1 | ||||
NM_030793.4 | Intron | NP_110420.3 | ||||
XM_005268513.1 | Intron | XP_005268570.1 | ||||
XM_006714797.1 | Intron | XP_006714860.1 | ||||
XM_011537684.2 | Intron | XP_011535986.1 | ||||
XM_017009899.1 | Intron | XP_016865388.1 | ||||
XM_017009900.1 | Intron | XP_016865389.1 | ||||
XM_017009901.1 | Intron | XP_016865390.1 | ||||
XM_017009902.1 | Intron | XP_016865391.1 |
LOC102546294 - uncharacterized LOC102546294 | ||||||
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There are no transcripts associated with this gene. |