Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs762258694
- Species
- Homo sapiens
- Symbol
- rs762258694
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT1L
- Location
- 1:185137687
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:185137687T>C
- HGVS.c name
- ENSEMBL:ENST00000367506.10:c.1432A>G
- ENSEMBL:ENST00000458395.1:c.304A>G
- HGVS.p name
- ENSP00000356476:p.Thr478Ala
- ENSP00000414339:p.Thr102Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:185118101...185157537 (39.44 kb)
- Assembly version
- Not Available
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