Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs376086109
- Species
- Homo sapiens
- Symbol
- rs376086109
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRIQ1
- Location
- 12:85244814
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:85244814C>T
- HGVS.c name
- ENSEMBL:ENST00000393217.7:c.5042C>T
- ENSEMBL:ENST00000528777.3:n.381C>T
- HGVS.p name
- ENSP00000376910:p.Thr1681Met
- ENSP00000497021:p.Thr9Met
- 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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