Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs372395537
- Species
- Homo sapiens
- Symbol
- rs372395537
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STT3B
- Location
- 3:31619800
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.31619800A>C
- HGVS.c name
- ENSEMBL:ENST00000295770.4:c.1297A>C
- ENSEMBL:ENST00000423527.5:n.1324A>C
- HGVS.p name
- :p.Ile287Leu
- ENSP00000295770:p.Ile433Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:31532638...31638548 (105.91 kb)
- Assembly version
- Not Available
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