Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs587658173
- Species
- Homo sapiens
- Symbol
- rs587658173
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PACS2
- Location
- 14:105369908
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000014.9:g.105369908C>T
- HGVS.c name
- ENSEMBL:ENST00000325438.12:c.801+8C>T
- ENSEMBL:ENST00000430725.6:c.576+8C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:105300563...105398147 (97.58 kb)
- Assembly version
- Not Available
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