Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PYROXD2 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PYROXD2 - pyridine nucleotide-disulphide oxidoreductase domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032709.2 | 1644 | Missense Mutation | ACC,GCC | T,A 533 | NP_116098.2 | |
XM_011540293.2 | 1644 | Missense Mutation | ACC,GCC | T,A 567 | XP_011538595.1 | |
XM_011540301.2 | 1644 | Missense Mutation | ACC,GCC | T,A 264 | XP_011538603.1 | |
XM_017016835.1 | 1644 | Missense Mutation | ACC,GCC | T,A 533 | XP_016872324.1 | |
XM_017016836.1 | 1644 | Intron | XP_016872325.1 | |||
XM_017016837.1 | 1644 | Intron | XP_016872326.1 | |||
XM_017016838.1 | 1644 | Missense Mutation | ACC,GCC | T,A 412 | XP_016872327.1 | |
XM_017016839.1 | 1644 | Missense Mutation | ACC,GCC | T,A 412 | XP_016872328.1 | |
XM_017016840.1 | 1644 | Missense Mutation | ACC,GCC | T,A 412 | XP_016872329.1 | |
XM_017016841.1 | 1644 | Missense Mutation | ACC,GCC | T,A 412 | XP_016872330.1 |
Set Membership: |
HapMap |