Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs575587861
- Species
- Homo sapiens
- Symbol
- rs575587861
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT5
- Location
- 14:60976122
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)14:60976122C>T
- HGVS.c name
- ENSEMBL:ENST00000261249.7:c.797G>A
- RefSeq:NM_001350253.1:c.881G>A
- HGVS.p name
- ENSP00000261249:p.Arg266Gln
- NP_001337182:p.Arg294Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:60971441...60981690 (10.25 kb)
- Assembly version
- Not Available
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