Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGAGTTTCCAGTGTTTGGGGAAG[G/T]GGAGGGTGTACTTCTTGTTGGAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
83 submissions
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Phenotype: |
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Literature Links: |
EXO5 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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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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EXO5 - exonuclease 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022774.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | NP_073611.1 | |
XM_005271125.3 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_005271182.1 | |
XM_005271126.3 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_005271183.1 | |
XM_005271128.3 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_005271185.1 | |
XM_011541970.2 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_011540272.1 | |
XM_017002099.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857588.1 | |
XM_017002100.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857589.1 | |
XM_017002101.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857590.1 | |
XM_017002102.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857591.1 | |
XM_017002103.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857592.1 | |
XM_017002104.1 | 947 | Missense Mutation | GGG,GTG | G,V 172 | XP_016857593.1 |