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TCGTGGCAGGAGTGGGCAGAATGGG[A/G]TGCATTTTACAGAAGAGTCACAGAG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616637 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928766 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) - Not Available | ||||||
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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LOC101928766 - uncharacterized LOC101928766 | ||||||
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There are no transcripts associated with this gene. |
TBC1D16 - TBC1 domain family member 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271844.1 | 6999 | UTR 3 | NP_001258773.1 | |||
NM_001271845.1 | 6999 | UTR 3 | NP_001258774.1 | |||
NM_001271846.1 | 6999 | Intron | NP_001258775.1 | |||
NM_019020.3 | 6999 | UTR 3 | NP_061893.2 | |||
XM_005257049.2 | 6999 | UTR 3 | XP_005257106.1 | |||
XM_005257050.3 | 6999 | UTR 3 | XP_005257107.1 | |||
XM_005257052.3 | 6999 | Intron | XP_005257109.1 | |||
XM_006721694.3 | 6999 | UTR 3 | XP_006721757.1 | |||
XM_006721695.3 | 6999 | Intron | XP_006721758.1 | |||
XM_011524322.2 | 6999 | UTR 3 | XP_011522624.1 | |||
XM_011524323.2 | 6999 | UTR 3 | XP_011522625.2 | |||
XM_011524324.2 | 6999 | UTR 3 | XP_011522626.1 | |||
XM_017024185.1 | 6999 | Intron | XP_016879674.1 | |||
XM_017024186.1 | 6999 | UTR 3 | XP_016879675.1 | |||
XM_017024187.1 | 6999 | UTR 3 | XP_016879676.1 | |||
XM_017024188.1 | 6999 | UTR 3 | XP_016879677.1 |
Set Membership: |
HapMap |