Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1384864058
- Species
- Homo sapiens
- Symbol
- rs1384864058
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TECPR2
- Location
- 14:102434980
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)14:102434980G>T
- HGVS.c name
- ENSEMBL:ENST00000359520.12:c.2163G>T
- ENSEMBL:ENST00000558678.1:c.2163G>T
- HGVS.p name
- ENSP00000352510:p.Val721=
- ENSP00000453671:p.Val721=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:102362941...102502477 (139.54 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction