Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs774667879
- Species
- Homo sapiens
- Symbol
- rs774667879
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RO60
- Location
- 1:193069188
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:193069188C>T
- HGVS.c name
- ENSEMBL:ENST00000367441.1:c.134C>T
- ENSEMBL:ENST00000367443.5:c.134C>T
- HGVS.p name
- ENSP00000356411:p.Thr45Ile
- ENSP00000356413:p.Thr45Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:193059454...193091777 (32.32 kb)
- Assembly version
- Not Available
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