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- SNP ID:
- rs1200425
- Gene
-
LOC105375077RUNX2 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.6: 45559395 - 45559395 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TACCTATAGATTTGGAATGGCTTTT[A/G]GAATGGAGAAATTATGGGGAGTTTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600211
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Literature Links: |
LOC105375077 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| LOC105375077 - uncharacterized LOC105375077 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| RUNX2 - runt related transcription factor 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001015051.3 | Intron | NP_001015051.3 | ||||
| NM_001024630.3 | Intron | NP_001019801.3 | ||||
| NM_001278478.1 | Intron | NP_001265407.1 | ||||
| XM_006715232.1 | Intron | XP_006715295.1 | ||||
| XM_011514960.2 | Intron | XP_011513262.1 | ||||
| XM_011514961.2 | Intron | XP_011513263.1 | ||||
| XM_011514962.2 | Intron | XP_011513264.1 | ||||
| XM_011514963.2 | Intron | XP_011513265.1 | ||||
| XM_011514964.2 | Intron | XP_011513266.1 | ||||
| XM_011514965.2 | Intron | XP_011513267.1 | ||||
| XM_011514966.2 | Intron | XP_011513268.1 | ||||
| XM_017011391.1 | Intron | XP_016866880.1 | ||||
| XM_017011392.1 | Intron | XP_016866881.1 | ||||
| XM_017011393.1 | Intron | XP_016866882.1 | ||||
| XM_017011394.1 | Intron | XP_016866883.1 | ||||
| XM_017011395.1 | Intron | XP_016866884.1 | ||||
| XM_017011396.1 | Intron | XP_016866885.1 | ||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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