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TGATTATAAGGAAATAGCGTTGCCA[C/T]TGTGAACCACTTATAAAAAGCGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603709 MIM: 182520 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAM22 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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ADAM22 - ADAM metallopeptidase domain 22 | ||||||
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There are no transcripts associated with this gene. |
LOC102723885 - uncharacterized LOC102723885 | ||||||
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There are no transcripts associated with this gene. |
SRI - sorcin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256891.1 | Intron | NP_001243820.1 | ||||
NM_001256892.1 | Intron | NP_001243821.1 | ||||
NM_003130.3 | Intron | NP_003121.1 | ||||
NM_198901.1 | Intron | NP_944490.1 | ||||
XM_011516528.1 | Intron | XP_011514830.1 |
Set Membership: |
HapMap |