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TTTCAAAAGTGCATCTCGTAGTGCC[A/C]ACTGTAAGATAAAAAAGTATTGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607469 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NAAA 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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NAAA - N-acylethanolamine acid amidase | ||||||
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There are no transcripts associated with this gene. |
SDAD1 - SDA1 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288983.1 | 2195 | Intron | NP_001275912.1 | |||
NM_001288984.1 | 2195 | Intron | NP_001275913.1 | |||
NM_018115.3 | 2195 | Intron | NP_060585.2 | |||
XM_005263102.4 | 2195 | Missense Mutation | TGG,TTG | W,L 648 | XP_005263159.1 | |
XM_005263105.4 | 2195 | Intron | XP_005263162.1 | |||
XM_017008354.1 | 2195 | Intron | XP_016863843.1 | |||
XM_017008355.1 | 2195 | Intron | XP_016863844.1 |