Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141588771
- Species
- Homo sapiens
- Symbol
- rs141588771
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AVPI1
- Location
- 10:97679752
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.97679752C>T
- HGVS.c name
- ENSEMBL:ENST00000370626.4:c.154G>A
- HGVS.p name
- ENSP00000359660:p.Glu52Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:97677424...97687241 (9.82 kb)
- Assembly version
- Not Available
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