Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199522267
- Species
- Homo sapiens
- Symbol
- rs199522267
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLTP
- Location
- 12:109855720
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:109855720G>A
- HGVS.c name
- ENSEMBL:ENST00000318348.9:c.346C>T
- ENSEMBL:ENST00000536390.5:n.409C>T
- HGVS.p name
- ENSP00000315263:p.Arg116Trp
- ENSP00000440136:p.Ala89Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109850945...109880541 (29.60 kb)
- Assembly version
- Not Available
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