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CTCATCCAGGGGCTGAGAGACGGCG[A/G]GACGCTGGGGCAGGGCACACTGGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606249 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C9orf129 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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C9orf129 - chromosome 9 open reading frame 129 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098808.1 | 931 | Silent Mutation | TCC,TCT | S,S 189 | NP_001092278.1 | |
XM_006717117.3 | 931 | Silent Mutation | TCC,TCT | S,S 189 | XP_006717180.1 |