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CATGCGCCTCCAGTCCCTGCAGCGC[A/G]CCCAGCAGCGGGCCAGGCGGCCCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
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Literature Links: |
C1orf159 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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C1orf159 - chromosome 1 open reading frame 159 | ||||||
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There are no transcripts associated with this gene. |
LOC100288175 - uncharacterized LOC100288175 | ||||||
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There are no transcripts associated with this gene. |
LOC105378948 - uncharacterized LOC105378948 | ||||||
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There are no transcripts associated with this gene. |
RNF223 - ring finger protein 223 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205252.1 | 867 | Missense Mutation | GCG,GTG | A,V 189 | NP_001192181.1 | |
XM_017001286.1 | 867 | Missense Mutation | GCG,GTG | A,V 189 | XP_016856775.1 | |
XM_017001287.1 | 867 | Intron | XP_016856776.1 |