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ATAAGGCAGATTTACCTTTTCAAAA[A/C]TCACATATTCAGCTGCTGGGAAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608889 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACMSD PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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ACMSD - aminocarboxymuconate semialdehyde decarboxylase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307983.1 | Intron | NP_001294912.1 | ||||
NM_138326.2 | Intron | NP_612199.2 | ||||
XM_005263586.4 | Intron | XP_005263643.1 | ||||
XM_005263588.4 | Intron | XP_005263645.1 | ||||
XM_005263589.4 | Intron | XP_005263646.1 | ||||
XM_005263590.4 | Intron | XP_005263647.1 | ||||
XM_011510592.2 | Intron | XP_011508894.1 | ||||
XM_017003325.1 | Intron | XP_016858814.1 | ||||
XM_017003326.1 | Intron | XP_016858815.1 |