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CCCCAGGAAGCCCAAATGGGAGGAG[A/G]AGGAGATGGAGGAAGACCTCGGGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603265 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARID3A 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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ARID3A - AT-rich interaction domain 3A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005224.2 | 843 | Missense Mutation | AAG,GAG | K,E 130 | NP_005215.1 | |
XM_005259513.4 | 843 | Missense Mutation | AAG,GAG | K,E 130 | XP_005259570.1 | |
XM_005259514.4 | 843 | Missense Mutation | AAG,GAG | K,E 130 | XP_005259571.1 | |
XM_017026445.1 | 843 | Missense Mutation | AAG,GAG | K,E 130 | XP_016881934.1 | |
XM_017026446.1 | 843 | Intron | XP_016881935.1 | |||
XM_017026447.1 | 843 | Intron | XP_016881936.1 |