Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766566969
- Species
- Homo sapiens
- Symbol
- rs766566969
- Category
- Variant
- Variant type
- SNP
- Overlaps
- OSTF1
- Location
- 9:75140852
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000009.12:g.75140852G>C
- HGVS.c name
- ENSEMBL:ENST00000346234.7:c.506G>C
- HGVS.p name
- ENSP00000340836:p.Arg169Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:75088514...75147265 (58.75 kb)
- Assembly version
- Not Available
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