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TGACACCTGCCCCTCCTTTCCTTCT[A/C]TGGCAGGCTCAGCATCTCTGCCCCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616879 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBC1D22A 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) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba)
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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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TBC1D22A - TBC1 domain family member 22A | ||||||
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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 |
Set Membership: |
HapMap |