Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1488761832
- Species
- Homo sapiens
- Symbol
- rs1488761832
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LZTFL1
- Location
- 3:45835659
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:45835659C>A
- HGVS.c name
- ENSEMBL:ENST00000296135.11:c.254G>T
- ENSEMBL:ENST00000411866.5:n.267G>T
- HGVS.p name
- ENSP00000296135:p.Arg85Leu
- ENSP00000412240:p.Arg68Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:45823316...45916042 (92.73 kb)
- Assembly version
- Not Available
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