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AGCTGCTCATGTATAATTTTAAAGC[A/T]ATTTTTGCATGGCTCACTCGAGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603136 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CUL3 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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CUL3 - cullin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001257197.1 | 6627 | UTR 3 | NP_001244126.1 | |||
NM_001257198.1 | 6627 | UTR 3 | NP_001244127.1 | |||
NM_003590.4 | 6627 | UTR 3 | NP_003581.1 | |||
XM_006712800.2 | 6627 | Intron | XP_006712863.2 | |||
XM_011511994.2 | 6627 | Intron | XP_011510296.1 | |||
XM_011511995.1 | 6627 | Intron | XP_011510297.1 | |||
XM_011511996.2 | 6627 | Intron | XP_011510298.1 |