Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1258933474
- Species
- Homo sapiens
- Symbol
- rs1258933474
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLMN
- Location
- 1:92290197
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice donor variant
- HGVS.g name
- (GRCh38)1:92290197C>T
- HGVS.c name
- ENSEMBL:ENST00000370360.8:c.394+1G>A
- ENSEMBL:ENST00000495106.5:n.487+1G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:92246402...92370844 (124.44 kb)
- Assembly version
- Not Available
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