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CTGTAGCTGCTCACCGAGCTGCTGA[A/G]AAGAGCATCAATCTTCTCCTCCTCT
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 | |||
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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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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 | 1449 | Missense Mutation | CTC,TTC | L,F 484 | NP_001180243.1 | |
NM_001193315.1 | 1449 | Missense Mutation | CTC,TTC | L,F 484 | NP_001180244.1 | |
NM_001193316.1 | 1449 | Missense Mutation | CTC,TTC | L,F 435 | NP_001180245.1 | |
NM_001193317.1 | 1449 | Missense Mutation | CTC,TTC | L,F 484 | NP_001180246.1 | |
NM_022067.3 | 1449 | Missense Mutation | CTC,TTC | L,F 484 | NP_071350.2 | |
XM_011537066.1 | 1449 | Missense Mutation | CTC,TTC | L,F 453 | XP_011535368.1 | |
XM_017021579.1 | 1449 | Missense Mutation | CTC,TTC | L,F 453 | XP_016877068.1 | |
XM_017021580.1 | 1449 | Intron | XP_016877069.1 | |||
XM_017021581.1 | 1449 | Intron | XP_016877070.1 |