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TATTTTCATGATCAAGTCTGATGAT[A/T]TGAAGAAGAGAAGAGAGCCTCACAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604978 MIM: 615857 | ||||||||||||||||||||
Literature Links: |
NUDT21 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 |
NUDT21 - nudix hydrolase 21 | ||||||
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There are no transcripts associated with this gene. |
OGFOD1 - 2-oxoglutarate and iron dependent oxygenase domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324357.1 | 478 | Missense Mutation | ATG,TTG | M,L 103 | NP_001311286.1 | |
NM_001324358.1 | 478 | Missense Mutation | ATG,TTG | M,L 49 | NP_001311287.1 | |
NM_001324359.1 | 478 | Missense Mutation | ATG,TTG | M,L 7 | NP_001311288.1 | |
NM_001324360.1 | 478 | Missense Mutation | ATG,TTG | M,L 7 | NP_001311289.1 | |
NM_001324361.1 | 478 | Missense Mutation | ATG,TTG | M,L 49 | NP_001311290.1 | |
NM_001324362.1 | 478 | UTR 5 | NP_001311291.1 | |||
NM_001324363.1 | 478 | Missense Mutation | ATG,TTG | M,L 104 | NP_001311292.1 | |
NM_018233.3 | 478 | Missense Mutation | ATG,TTG | M,L 104 | NP_060703.3 |