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TGTTTTTTACTAATTACTGAAAATA[A/G]GGGTACTCCTTTTTTATTAGAAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604649 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TBCD PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
TBCD - tubulin folding cofactor D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005993.4 | Intron | NP_005984.3 | ||||
XM_005256396.4 | Intron | XP_005256453.1 | ||||
XM_005256399.4 | Intron | XP_005256456.1 | ||||
XM_005256404.4 | Intron | XP_005256461.1 | ||||
XM_006722290.2 | Intron | XP_006722353.1 | ||||
XM_006722291.3 | Intron | XP_006722354.1 | ||||
XM_006722292.2 | Intron | XP_006722355.1 | ||||
XM_011523589.1 | Intron | XP_011521891.1 | ||||
XM_011523590.1 | Intron | XP_011521892.1 | ||||
XM_011523591.1 | Intron | XP_011521893.1 | ||||
XM_011523593.1 | Intron | XP_011521895.1 | ||||
XM_011523594.1 | Intron | XP_011521896.1 | ||||
XM_011523595.2 | Intron | XP_011521897.1 | ||||
XM_011523597.2 | Intron | XP_011521899.1 | ||||
XM_011523598.1 | Intron | XP_011521900.1 | ||||
XM_011523599.2 | Intron | XP_011521901.1 | ||||
XM_011523600.2 | Intron | XP_011521902.1 | ||||
XM_017024987.1 | Intron | XP_016880476.1 | ||||
XM_017024988.1 | Intron | XP_016880477.1 | ||||
XM_017024989.1 | Intron | XP_016880478.1 | ||||
XM_017024990.1 | Intron | XP_016880479.1 |