Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142991497
- Species
- Homo sapiens
- Symbol
- rs142991497
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STYXL1
- Location
- 7:76000934
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.76000934C>T
- HGVS.c name
- ENSEMBL:ENST00000340062.9:c.478G>A
- ENSEMBL:ENST00000359697.8:c.766G>A
- HGVS.p name
- ENSP00000343383:p.Ala160Thr
- ENSP00000352726:p.Ala256Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:75996337...76048004 (51.67 kb)
- Assembly version
- Not Available
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