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TTTTAGCGTCTCTTCTGCCCTATTT[C/T]GGACCAGGAGATGAGCAATGTTCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616880 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBC1D22B 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) - Not Available | ||||||
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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TBC1D22B - TBC1 domain family member 22B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017772.3 | Intron | NP_060242.2 | ||||
XM_011514738.2 | Intron | XP_011513040.1 | ||||
XM_011514739.1 | Intron | XP_011513041.1 |
Set Membership: |
HapMap |