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TTGTTCTCAAAGAGACCTTCATTGC[A/G]GGGGATTCCATGAGAACCATCAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613597 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HOGA1 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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HOGA1 - 4-hydroxy-2-oxoglutarate aldolase 1 | ||||||
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There are no transcripts associated with this gene. |
MORN4 - MORN repeat containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098831.1 | 636 | Intron | NP_001092301.1 | |||
NM_178832.3 | 636 | Missense Mutation | CGC,TGC | R,C 111 | NP_849154.1 | |
XM_011539250.2 | 636 | Missense Mutation | CGC,TGC | R,C 169 | XP_011537552.1 | |
XM_011539251.2 | 636 | Missense Mutation | CGC,TGC | R,C 111 | XP_011537553.1 |