Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs766067329
- Species
- Homo sapiens
- Symbol
- rs766067329
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRIQ1
- Location
- 12:85160670
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000012.12:g.85160670A>T
- HGVS.c name
- ENSEMBL:ENST00000393217.7:c.4778A>T
- ENSEMBL:ENST00000526363.1:c.40A>T
- HGVS.p name
- ENSP00000376910:p.Lys1593Ile
- ENSP00000431756:p.Asn14Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:85036314...85272805 (236.49 kb)
- Assembly version
- Not Available
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