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CCTTGGACGAAAGCGAAACCTTAAT[G/T]TTGCTAGCGACCCGAGAGCTCCGCC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609850 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBC1D1 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) - 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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TBC1D1 - TBC1 domain family member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001253912.1 | Intron | NP_001240841.1 | ||||
NM_001253913.1 | Intron | NP_001240842.1 | ||||
NM_001253914.1 | Intron | NP_001240843.1 | ||||
NM_001253915.1 | Intron | NP_001240844.1 | ||||
NM_015173.3 | Intron | NP_055988.2 | ||||
XM_005262646.2 | Intron | XP_005262703.1 | ||||
XM_005262647.2 | Intron | XP_005262704.1 | ||||
XM_005262649.2 | Intron | XP_005262706.1 | ||||
XM_006714001.2 | Intron | XP_006714064.1 | ||||
XM_011513659.2 | Intron | XP_011511961.1 | ||||
XM_011513660.2 | Intron | XP_011511962.1 | ||||
XM_011513662.2 | Intron | XP_011511964.1 | ||||
XM_011513663.2 | Intron | XP_011511965.1 | ||||
XM_011513664.2 | Intron | XP_011511966.1 | ||||
XM_011513665.2 | Intron | XP_011511967.1 | ||||
XM_011513666.2 | Intron | XP_011511968.1 | ||||
XM_011513668.2 | Intron | XP_011511970.1 | ||||
XM_011513670.2 | Intron | XP_011511972.1 | ||||
XM_017007918.1 | Intron | XP_016863407.1 | ||||
XM_017007919.1 | Intron | XP_016863408.1 | ||||
XM_017007920.1 | Intron | XP_016863409.1 | ||||
XM_017007921.1 | Intron | XP_016863410.1 | ||||
XM_017007922.1 | Intron | XP_016863411.1 |
Set Membership: |
HapMap |