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AGCAGGAGCAAAAGCATCCTTTCCC[A/G]TACCAGAGGAGAGTCCCGAAATTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604611 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PURG 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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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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PURG - purine rich element binding protein G | ||||||
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There are no transcripts associated with this gene. |
WRN - Werner syndrome RecQ like helicase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000553.4 | Intron | NP_000544.2 | ||||
XM_011544639.2 | Intron | XP_011542941.1 | ||||
XM_011544640.1 | Intron | XP_011542942.1 |
Set Membership: |
HapMap Validated |