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AGACGGCAAGCAGCAGAGGAATATC[A/G]CATCGGCCCAACTCACCAGATCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NOXRED1 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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NOXRED1 - NADP dependent oxidoreductase domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113475.2 | 496 | Missense Mutation | GCG,GTG | A,V 139 | NP_001106946.1 | |
XM_005267330.3 | 496 | Missense Mutation | GCG,GTG | A,V 139 | XP_005267387.1 | |
XM_011536427.2 | 496 | Missense Mutation | GCG,GTG | A,V 139 | XP_011534729.1 | |
XM_011536428.2 | 496 | Missense Mutation | GCG,GTG | A,V 139 | XP_011534730.1 | |
XM_011536429.2 | 496 | Missense Mutation | GCG,GTG | A,V 49 | XP_011534731.1 | |
XM_017020969.1 | 496 | Missense Mutation | GCG,GTG | A,V 139 | XP_016876458.1 | |
XM_017020970.1 | 496 | Intron | XP_016876459.1 |