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ACAGCAGCCAGCTTTGTATTGTAAT[A/G]CTATATTATGTAAATGTGATGAAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603390 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PDE8B 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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WDR41 - WD repeat domain 41 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018268.3 | 4073 | Intron | NP_060738.2 | |||
XM_005248551.4 | 4073 | Intron | XP_005248608.1 | |||
XM_005248552.3 | 4073 | Intron | XP_005248609.1 | |||
XM_011543505.2 | 4073 | Intron | XP_011541807.1 | |||
XM_011543507.2 | 4073 | Intron | XP_011541809.1 | |||
XM_017009606.1 | 4073 | Intron | XP_016865095.1 |