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TCCACTGGAGAGGGGGTGAAAGACT[G/T]CACAGAGCCCTGCTCCGGGGAGAAG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607679 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DOCK4 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)
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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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DOCK4 - dedicator of cytokinesis 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014705.3 | 6265 | Missense Mutation | AAG,CAG | K,Q 1822 | NP_055520.3 | |
XM_006716188.2 | 6265 | Missense Mutation | AAG,CAG | K,Q 1831 | XP_006716251.1 | |
XM_006716189.2 | 6265 | Missense Mutation | AAG,CAG | K,Q 1793 | XP_006716252.1 | |
XM_017012819.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1862 | XP_016868308.1 | |
XM_017012820.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1853 | XP_016868309.1 | |
XM_017012821.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1844 | XP_016868310.1 | |
XM_017012822.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1842 | XP_016868311.1 | |
XM_017012823.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1824 | XP_016868312.1 | |
XM_017012824.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1815 | XP_016868313.1 | |
XM_017012825.1 | 6265 | Missense Mutation | AAG,CAG | K,Q 1806 | XP_016868314.1 |
Set Membership: |
HapMap |