Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142093260
- Species
- Homo sapiens
- Symbol
- rs142093260
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IL10
- Location
- 1:206768663
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)1:206768663G>A
- HGVS.c name
- ENSEMBL:ENST00000367099.4:n.1515C>T
- ENSEMBL:ENST00000423557.1:c.510C>T
- HGVS.p name
- ENSP00000412237:p.Ala170=
- ENSP00000493073:p.Ala85=
- 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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