Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs765563550
- Species
- Homo sapiens
- Symbol
- rs765563550
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PRTFDC1
- Location
- 10:24851444
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)10:24851444T>C
- HGVS.c name
- ENSEMBL:ENST00000320152.11:c.574A>G
- ENSEMBL:ENST00000376378.5:c.554-1553A>G
- HGVS.p name
- ENSP00000318602:p.Asn192Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:24848614...24952606 (103.99 kb)
- Assembly version
- Not Available
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