Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs16992223
- Species
- Homo sapiens
- Symbol
- rs16992223
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LARGE1
- Location
- 22:33382239
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)22:33382239C>T
- HGVS.c name
- ENSEMBL:ENST00000354992.7:c.1006-195G>A
- ENSEMBL:ENST00000397394.8:c.1006-195G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:33066663...33922841 (856.18 kb)
- Assembly version
- Not Available
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