Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs568879359
- Species
- Homo sapiens
- Symbol
- rs568879359
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL10
- Location
- 1:206768666
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:206768666T>G
- HGVS.c name
- ENSEMBL:ENST00000367099.4:n.1512A>C
- ENSEMBL:ENST00000423557.1:c.507A>C
- HGVS.p name
- ENSP00000412237:p.Glu169Asp
- ENSP00000493073:p.Glu84Asp
- 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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