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AATGTCCTGTGAGGACCATTGAAAA[A/G]CTTGTTCTATGTTATGGCAAATGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608181 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKDD1A 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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ANKDD1A - ankyrin repeat and death domain containing 1A | ||||||
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There are no transcripts associated with this gene. |
SPG21 - spastic paraplegia 21 (autosomal recessive, Mast syndrome) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127889.4 | Intron | NP_001121361.1 | ||||
NM_001127890.4 | Intron | NP_001121362.1 | ||||
NM_016630.6 | Intron | NP_057714.1 | ||||
XM_005254437.4 | Intron | XP_005254494.1 | ||||
XM_017022297.1 | Intron | XP_016877786.1 | ||||
XM_017022298.1 | Intron | XP_016877787.1 |