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TTTAGAAGCTGCCAGTTTTCATGAC[A/G]TATTTGATAAAGTGTTTACAAATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CCDC173 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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CCDC173 - coiled-coil domain containing 173 | ||||||
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There are no transcripts associated with this gene. |
PHOSPHO2 - phosphatase, orphan 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008489.3 | 648 | Missense Mutation | ATA,GTA | I,V 117 | NP_001008489.1 | |
NM_001199285.1 | 648 | Missense Mutation | ATA,GTA | I,V 117 | NP_001186214.1 | |
NM_001199286.1 | 648 | Missense Mutation | ATA,GTA | I,V 117 | NP_001186215.1 | |
NM_001199287.1 | 648 | Missense Mutation | ATA,GTA | I,V 117 | NP_001186216.1 | |
NM_001199288.1 | 648 | Missense Mutation | ATA,GTA | I,V 117 | NP_001186217.1 |
PHOSPHO2-KLHL23 - PHOSPHO2-KLHL23 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199290.1 | 648 | Intron | NP_001186219.1 |