Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1567756588
- Species
- Homo sapiens
- Symbol
- rs1567756588
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BRCA1
- Location
- 17:43045752
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.43045752C>G
- HGVS.c name
- ENSEMBL:ENST00000352993.7:c.2092G>C
- ENSEMBL:ENST00000461221.5:n.5619G>C
- HGVS.p name
- ENSP00000312236:p.Asp698His
- ENSP00000417554:p.Asp1838His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:43044295...43170327 (126.03 kb)
- Assembly version
- Not Available
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