Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs140582774
- Species
- Homo sapiens
- Symbol
- rs140582774
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PGAP4
- Location
- 9:101476033
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)9:101476033C>G
- HGVS.c name
- ENSEMBL:ENST00000374847.5:c.1060G>C
- ENSEMBL:ENST00000374848.8:c.1060G>C
- HGVS.p name
- ENSP00000363980:p.Val354Leu
- ENSP00000363981:p.Val354Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:101473170...101533686 (60.52 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction