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- SNP ID:
- rs142624764
- Gene
-
GLYR1UBN1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.16: 4852953 - 4852953 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
CCCACAGGGTCCAGTTCACCTCTCT[C/G]CCAGGTTCCCTGAATCCTGCGTTTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610660
MIM: 609771
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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 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| UBN1 - ubinuclein 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001079514.2 | 840 | Silent Mutation | CTC,CTG | L,L 12 | NP_001072982.1 | |
| NM_001288656.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | NP_001275585.1 | |
| XM_005255277.3 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_005255334.1 | |
| XM_005255278.3 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_005255335.1 | |
| XM_005255279.3 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_005255336.1 | |
| XM_011522465.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_011520767.1 | |
| XM_011522466.2 | 840 | Intron | XP_011520768.1 | |||
| XM_011522467.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_011520769.1 | |
| XM_017023189.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_016878678.1 | |
| XM_017023190.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_016878679.1 | |
| XM_017023191.1 | 840 | Intron | XP_016878680.1 | |||
| XM_017023192.1 | 840 | Silent Mutation | CTC,CTG | L,L 12 | XP_016878681.1 | |
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