Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTACTGTGTGCGCCGGGGAGGCGCC[A/G]GCTTGTACTCGGCAGCGCGGGAATA
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 - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | 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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001015508.2 | 576 | Intron | NP_001015508.1 | |||
NM_001323311.1 | 576 | Intron | NP_001310240.1 | |||
NM_001323312.1 | 576 | Intron | NP_001310241.1 | |||
NM_013357.2 | 576 | Intron | NP_037489.1 |
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 | 576 | UTR 5 | NP_000544.2 | |||
XM_011544639.2 | 576 | UTR 5 | XP_011542941.1 | |||
XM_011544640.1 | 576 | Intron | XP_011542942.1 |
Set Membership: |
HapMap |