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CAGGAACAAAGAGTAGTGTCCCACA[A/G]TCTCCACGAAGAAGCGGACAAAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
DENND2A 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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DENND2A - DENN domain containing 2A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318052.1 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | NP_001304981.1 | |
NM_001318053.1 | 3231 | Intron | NP_001304982.1 | |||
NM_015689.4 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | NP_056504.3 | |
XM_005249977.3 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | XP_005250034.1 | |
XM_005249979.4 | 3231 | Intron | XP_005250036.1 | |||
XM_011516052.2 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | XP_011514354.1 | |
XM_011516053.2 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | XP_011514355.1 | |
XM_011516054.2 | 3231 | Missense Mutation | ACT,ATT | T,I 909 | XP_011514356.1 | |
XM_017011989.1 | 3231 | Missense Mutation | ACT,ATT | T,I 910 | XP_016867478.1 |