Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs79917141
- Species
- Homo sapiens
- Symbol
- rs79917141
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUDT21
- Location
- 16:56434354
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000016.10:g.56434354A>G
- HGVS.c name
- ENSEMBL:ENST00000300291.10:c.639T>C
- ENSEMBL:ENST00000563860.1:n.551T>C
- HGVS.p name
- ENSP00000300291:p.Ser213=
- ENSP00000454790:p.Ser147=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:56429133...56452199 (23.07 kb)
- Assembly version
- Not Available
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