Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1427896636
- Species
- Homo sapiens
- Symbol
- rs1427896636
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CFAP97
- Location
- 4:185175877
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:185175877G>A
- HGVS.c name
- ENSEMBL:ENST00000458385.7:c.1229C>T
- ENSEMBL:ENST00000502992.1:n.517C>T
- HGVS.p name
- ENSP00000409964:p.Thr410Ile
- ENSP00000423312:p.Thr410Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:185159665...185210248 (50.58 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction