Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs938126566
- Species
- Homo sapiens
- Symbol
- rs938126566
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC6A6
- Location
- 3:14484934
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:14484934C>T
- HGVS.c name
- ENSEMBL:ENST00000613060.4:c.2093C>T
- ENSEMBL:ENST00000618278.4:n.1986C>T
- HGVS.p name
- ENSP00000480890:p.Pro597Leu
- ENSP00000481625:p.Pro698Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:14402576...14489349 (86.77 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction