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GCTCTGGGATCTGTATACCCTCAGG[C/T]CATCGTGGAGTAGGAATGAGCTGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614855 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBC1D14 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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TBC1D14 - TBC1 domain family member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113361.1 | Intron | NP_001106832.1 | ||||
NM_001113363.1 | Intron | NP_001106834.1 | ||||
NM_001286805.1 | Intron | NP_001273734.1 | ||||
NM_020773.2 | Intron | NP_065824.2 | ||||
XM_005247986.2 | Intron | XP_005248043.1 | ||||
XM_006713895.2 | Intron | XP_006713958.1 | ||||
XM_011513507.2 | Intron | XP_011511809.1 | ||||
XM_011513508.1 | Intron | XP_011511810.1 | ||||
XM_011513513.2 | Intron | XP_011511815.1 | ||||
XM_017008477.1 | Intron | XP_016863966.1 | ||||
XM_017008478.1 | Intron | XP_016863967.1 | ||||
XM_017008479.1 | Intron | XP_016863968.1 | ||||
XM_017008480.1 | Intron | XP_016863969.1 |
Set Membership: |
HapMap |