Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs114355007
- Species
- Homo sapiens
- Symbol
- rs114355007
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT1L
- Location
- 1:185144020
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:185144020G>A
- HGVS.c name
- ENSEMBL:ENST00000367506.10:c.665C>T
- ENSEMBL:ENST00000487028.1:n.519C>T
- HGVS.p name
- ENSP00000356476:p.Ala222Val
- NP_001189352:p.Ala66Val
- 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