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CTCATATAAGCCCCTGTCTCCAGCC[A/G]CTAAGATCACCAACATCCCGTCATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610660 MIM: 614574 | ||||||||||||||||||||
Literature Links: |
GLYR1 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 |
GLYR1 - glyoxylate reductase 1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308096.1 | 1373 | Intron | NP_001295025.1 | |||
NM_001324096.1 | 1373 | Intron | NP_001311025.1 | |||
NM_001324097.1 | 1373 | Intron | NP_001311026.1 | |||
NM_001324098.1 | 1373 | Intron | NP_001311027.1 | |||
NM_032569.3 | 1373 | Intron | NP_115958.2 | |||
XM_005255639.4 | 1373 | Intron | XP_005255696.2 | |||
XM_011522716.2 | 1373 | Missense Mutation | GCG,GTG | A,V 398 | XP_011521018.1 | |
XM_011522717.1 | 1373 | Intron | XP_011521019.1 | |||
XM_017023786.1 | 1373 | Intron | XP_016879275.1 | |||
XM_017023787.1 | 1373 | Intron | XP_016879276.1 | |||
XM_017023788.1 | 1373 | Intron | XP_016879277.1 | |||
XM_017023789.1 | 1373 | Intron | XP_016879278.1 |
ROGDI - rogdi homolog | ||||||
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There are no transcripts associated with this gene. |