Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs750010814
- Species
- Homo sapiens
- Symbol
- rs750010814
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL10
- Location
- 1:206772315
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)1:206772315G>A
- HGVS.c name
- ENSEMBL:ENST00000423557.1:c.121C>T
- ENSEMBL:ENST00000656872.2:c.-149+1485G>A
- HGVS.p name
- ENSP00000412237:p.Leu41Phe
- ENSP00000499509:p.Leu2Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:206767602...206774541 (6.94 kb)
- Assembly version
- Not Available
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