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AGAAATACATAGGTCTCAGGATTAG[A/G]GAGCATGCATTCTGGAGCACACCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612396 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ALLC 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ALLC - allantoicase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018436.3 | Intron | NP_060906.3 | ||||
XM_011510369.2 | Intron | XP_011508671.1 | ||||
XM_011510370.2 | Intron | XP_011508672.1 | ||||
XM_017004495.1 | Intron | XP_016859984.1 | ||||
XM_017004496.1 | Intron | XP_016859985.1 | ||||
XM_017004497.1 | Intron | XP_016859986.1 | ||||
XM_017004498.1 | Intron | XP_016859987.1 |