Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770116608
- Species
- Homo sapiens
- Symbol
- rs770116608
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FRMD4A
- Location
- 10:13810846
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)10:13810846C>T
- HGVS.c name
- ENSEMBL:ENST00000264546.10:c.273G>A
- ENSEMBL:ENST00000342409.3:n.603G>A
- HGVS.p name
- ENSP00000264546:p.Lys91=
- ENSP00000350032:p.Lys58=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:13643706...14462142 (818.44 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction