Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs80348727
- Species
- Homo sapiens
- Symbol
- rs80348727
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STT3B
- Location
- 3:31621984
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)3:31621984C>T
- HGVS.c name
- ENSEMBL:ENST00000295770.4:c.1328-113C>T
- ENSEMBL:ENST00000462235.6:c.890-113C>T
- HGVS.p name
- Not Available
- 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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