Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs367936727
- Species
- Homo sapiens
- Symbol
- rs367936727
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GATB
- Location
- 4:151717018
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:151717018T>C
- HGVS.c name
- ENSEMBL:ENST00000263985.11:c.498A>G
- ENSEMBL:ENST00000503160.5:n.390-17A>G
- HGVS.p name
- ENSP00000263985:p.Ile166Met
- ENSP00000420831:p.Ile166Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:151670504...151761007 (90.50 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction