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GGTGACATATGTCAATTGAATCCAC[A/G]TATCTTTTTGCTTTTAAGTAATTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612014 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC100506124 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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LOC100506124 - uncharacterized LOC100506124 | ||||||
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There are no transcripts associated with this gene. |
TTC21B - tetratricopeptide repeat domain 21B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024753.4 | 3953 | Silent Mutation | NP_079029.3 | |||
XM_006712761.1 | 3953 | Intron | XP_006712824.1 | |||
XM_011511871.2 | 3953 | Silent Mutation | XP_011510173.1 | |||
XM_011511872.2 | 3953 | UTR 3 | XP_011510174.1 | |||
XM_017004967.1 | 3953 | Intron | XP_016860456.1 | |||
XM_017004968.1 | 3953 | Silent Mutation | XP_016860457.1 | |||
XM_017004969.1 | 3953 | Nonsense Mutation | XP_016860458.1 |