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GCCAGACCACGACGCAGATGGACAC[C/T]GTGGGCCGGACCTGGAGGGGGCAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
28 submissions
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Phenotype: |
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Literature Links: |
TTLL10 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 | 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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TTLL10 - tubulin tyrosine ligase like 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130045.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | NP_001123517.1 | |
NM_153254.2 | 599 | Missense Mutation | CGT,TGT | R,C 24 | NP_694986.2 | |
XM_005244738.1 | 599 | Missense Mutation | CGT,TGT | R,C 24 | XP_005244795.1 | |
XM_011541177.2 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_011539479.1 | |
XM_017000906.1 | 599 | Missense Mutation | CGT,TGT | R,C 70 | XP_016856395.1 | |
XM_017000907.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856396.1 | |
XM_017000908.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856397.1 | |
XM_017000909.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856398.1 | |
XM_017000910.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856399.1 | |
XM_017000911.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856400.1 | |
XM_017000912.1 | 599 | Missense Mutation | CGT,TGT | R,C 97 | XP_016856401.1 |
TTLL10-AS1 - TTLL10 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |