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TBC1D22A
TBC1D22A-AS1GTTCTGGCTGTCAGTGGGAGGTTCC[A/G]ACTCTGCACATGCTGGCACTCAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TBC1D22A 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)
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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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| TBC1D22A - TBC1 domain family member 22A | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001284303.1 | Intron | NP_001271232.1 | ||||
| NM_001284304.1 | Intron | NP_001271233.1 | ||||
| NM_001284305.1 | Intron | NP_001271234.1 | ||||
| NM_014346.3 | Intron | NP_055161.1 | ||||
| XM_005261496.1 | Intron | XP_005261553.1 | ||||
| XM_011530099.1 | Intron | XP_011528401.1 | ||||
| XM_011530100.2 | Intron | XP_011528402.1 | ||||
| XM_011530101.2 | Intron | XP_011528403.1 | ||||
| XM_011530102.2 | Intron | XP_011528404.1 | ||||
| XM_017028742.1 | Intron | XP_016884231.1 | ||||
| XM_017028743.1 | Intron | XP_016884232.1 | ||||
| XM_017028744.1 | Intron | XP_016884233.1 | ||||
| XM_017028745.1 | Intron | XP_016884234.1 | ||||
| XM_017028746.1 | Intron | XP_016884235.1 | ||||
| XM_017028747.1 | Intron | XP_016884236.1 | ||||
| TBC1D22A-AS1 - TBC1D22A antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Set Membership: |
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