Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201126720
- Species
- Homo sapiens
- Symbol
- rs201126720
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TPRG1L
- Location
- 1:3625757
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:3625757C>T
- HGVS.c name
- ENSEMBL:ENST00000344579.5:c.293+242C>T
- ENSEMBL:ENST00000378344.7:c.338C>T
- HGVS.p name
- ENSP00000367595:p.Thr113Met
- NP_877429:p.Thr113Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:3625015...3630127 (5.11 kb)
- Assembly version
- Not Available
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