Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs138631745
- Species
- Homo sapiens
- Symbol
- rs138631745
- Category
- Variant
- Variant type
- SNP
- Overlaps
- OSTF1
- Location
- 9:75146721
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:75146721G>T
- HGVS.c name
- ENSEMBL:ENST00000346234.7:c.625G>T
- HGVS.p name
- ENSP00000340836:p.Asp209Tyr
- 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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