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GTTCTTGTGCAAAATTTCGACAACC[C/G]GATGGAAGCCAATGGGTGCTCTCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613401 | ||||||||||||||||||||
Literature Links: |
NOXRED1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NOXRED1 - NADP dependent oxidoreductase domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
VIPAS39 - VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193314.1 | 1225 | Missense Mutation | CCG,CGG | P,R 409 | NP_001180243.1 | |
NM_001193315.1 | 1225 | Missense Mutation | CCG,CGG | P,R 409 | NP_001180244.1 | |
NM_001193316.1 | 1225 | Missense Mutation | CCG,CGG | P,R 360 | NP_001180245.1 | |
NM_001193317.1 | 1225 | Missense Mutation | CCG,CGG | P,R 409 | NP_001180246.1 | |
NM_022067.3 | 1225 | Missense Mutation | CCG,CGG | P,R 409 | NP_071350.2 | |
XM_011537066.1 | 1225 | Missense Mutation | CCG,CGG | P,R 378 | XP_011535368.1 | |
XM_017021579.1 | 1225 | Missense Mutation | CCG,CGG | P,R 378 | XP_016877068.1 | |
XM_017021580.1 | 1225 | Intron | XP_016877069.1 | |||
XM_017021581.1 | 1225 | Intron | XP_016877070.1 |