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TCCAGAGAATGTACAAGGGCTGTCC[C/G]GGATCCTGATGTAACTTCATATTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600382 MIM: 603617 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DENND4A 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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DENND4A - DENN domain containing 4A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144823.2 | 5571 | Silent Mutation | CCC,CCG | P,P 1774 | NP_001138295.1 | |
NM_001320835.1 | 5571 | Silent Mutation | CCC,CCG | P,P 1775 | NP_001307764.1 | |
NM_005848.4 | 5571 | Silent Mutation | CCC,CCG | P,P 1731 | NP_005839.3 | |
XM_005254120.4 | 5571 | Silent Mutation | CCC,CCG | P,P 1775 | XP_005254177.1 | |
XM_005254121.3 | 5571 | Silent Mutation | CCC,CCG | P,P 1731 | XP_005254178.1 | |
XM_005254122.4 | 5571 | Silent Mutation | CCC,CCG | P,P 1041 | XP_005254179.1 | |
XM_006720371.3 | 5571 | Silent Mutation | CCC,CCG | P,P 1775 | XP_006720434.1 | |
XM_011521156.2 | 5571 | Intron | XP_011519458.1 | |||
XM_011521157.2 | 5571 | Silent Mutation | CCC,CCG | P,P 1259 | XP_011519459.1 | |
XM_017021862.1 | 5571 | Silent Mutation | CCC,CCG | P,P 1775 | XP_016877351.1 | |
XM_017021863.1 | 5571 | Silent Mutation | CCC,CCG | P,P 1731 | XP_016877352.1 | |
XM_017021864.1 | 5571 | Silent Mutation | CCC,CCG | P,P 1775 | XP_016877353.1 | |
XM_017021865.1 | 5571 | Silent Mutation | CCC,CCG | P,P 997 | XP_016877354.1 |
SLC24A1 - solute carrier family 24 member 1 | ||||||
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There are no transcripts associated with this gene. |