Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs763566646
- Species
- Homo sapiens
- Symbol
- rs763566646
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SAP30L
- Location
- 5:154446644
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:154446644C>A
- HGVS.c name
- ENSEMBL:ENST00000297109.11:c.40C>A
- ENSEMBL:ENST00000519683.1:n.23C>A
- HGVS.p name
- ENSP00000297109:p.Pro14Thr
- XP_047273665:p.Pro14Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:154445997...154461053 (15.06 kb)
- Assembly version
- Not Available
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