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- SNP ID:
- rs138448676
- Gene
-
MIR4757OSR1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.2: 19352348 - 19352348 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
CGTCTTGTGGACAGCGAGAGTCCTG[A/G]ACTGGCAGAATCCTTTCCCACACTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608891
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Literature Links: |
MIR4757 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 |
| MIR4757 - microRNA 4757 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| OSR1 - odd-skipped related transciption factor 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_145260.2 | 1900 | Missense Mutation | TCC,TTC | S,F 243 | NP_660303.1 | |
| XM_006711942.3 | 1900 | Missense Mutation | TCC,TTC | S,F 243 | XP_006712005.1 | |
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