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CCCTGATTATGAATAGAACCTTTCC[C/T]TTTTAATAACTTGTCTTTTAATATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607111 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC169 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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CCDC169 - coiled-coil domain containing 169 | ||||||
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There are no transcripts associated with this gene. |
CCDC169-SOHLH2 - CCDC169-SOHLH2 readthrough | ||||||
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There are no transcripts associated with this gene. |
SPG20 - spastic paraplegia 20 (Troyer syndrome) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142294.1 | 3197 | UTR 3 | NP_001135766.1 | |||
NM_001142295.1 | 3197 | UTR 3 | NP_001135767.1 | |||
NM_001142296.1 | 3197 | UTR 3 | NP_001135768.1 | |||
NM_015087.4 | 3197 | UTR 3 | NP_055902.1 | |||
XM_005266313.4 | 3197 | UTR 3 | XP_005266370.1 | |||
XM_005266314.3 | 3197 | UTR 3 | XP_005266371.1 | |||
XM_005266315.3 | 3197 | UTR 3 | XP_005266372.1 | |||
XM_005266317.3 | 3197 | UTR 3 | XP_005266374.1 | |||
XM_011535012.2 | 3197 | UTR 3 | XP_011533314.1 |