Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs377360983
- Species
- Homo sapiens
- Symbol
- rs377360983
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT1L
- Location
- 1:185137723
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:185137723C>G
- HGVS.c name
- ENSEMBL:ENST00000367506.10:c.1396G>C
- ENSEMBL:ENST00000458395.1:c.268G>C
- HGVS.p name
- ENSP00000356476:p.Val466Leu
- ENSP00000414339:p.Val90Leu
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction