Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs145942606
- Species
- Homo sapiens
- Symbol
- rs145942606
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STYXL1
- Location
- 7:76030435
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)7:76030435T>C
- HGVS.c name
- ENSEMBL:ENST00000340062.9:c.89A>G
- ENSEMBL:ENST00000359697.8:c.89A>G
- HGVS.p name
- ENSP00000343383:p.Tyr30Cys
- ENSP00000352726:p.Tyr30Cys
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction