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- SNP ID:
- rs199678307
- Gene
-
OVOL1OVOL1-AS1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 65794610 - 65794610 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CTGCCAGAAGGCCTTCACCTACCAG[C/T]GCATGCTGAACCGCCACATGAAGTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602313
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Literature Links: |
OVOL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| OVOL1 - ovo like transcriptional repressor 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_004561.3 | 731 | Missense Mutation | CGC,TGC | R,C 131 | NP_004552.2 | |
| XM_005274018.3 | 731 | Missense Mutation | CGC,TGC | R,C 69 | XP_005274075.1 | |
| XM_011545067.2 | 731 | Missense Mutation | CGC,TGC | R,C 69 | XP_011543369.1 | |
| XM_011545068.2 | 731 | Missense Mutation | CGC,TGC | R,C 69 | XP_011543370.1 | |
| XM_017017837.1 | 731 | Missense Mutation | CGC,TGC | R,C 69 | XP_016873326.1 | |
| XM_017017838.1 | 731 | Missense Mutation | CGC,TGC | R,C 69 | XP_016873327.1 | |
| OVOL1-AS1 - OVOL1 antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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