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TTTGATGGCGACGACTTTGATGATG[C/T]GGAGGAGGATGAAGGGCTAGATGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604414 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C22orf23 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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C22orf23 - chromosome 22 open reading frame 23 | ||||||
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There are no transcripts associated with this gene. |
POLR2F - RNA polymerase II subunit F | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301129.1 | 172 | UTR 5 | NP_001288058.1 | |||
NM_001301130.1 | 172 | Missense Mutation | GCG,GTG | A,V 16 | NP_001288059.1 | |
NM_001301131.1 | 172 | Missense Mutation | GCG,GTG | A,V 16 | NP_001288060.1 | |
NM_021974.4 | 172 | Missense Mutation | GCG,GTG | A,V 16 | NP_068809.1 | |
XM_017028832.1 | 172 | Missense Mutation | GCG,GTG | A,V 16 | XP_016884321.1 |