Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs140202814
- Species
- Homo sapiens
- Symbol
- rs140202814
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT61B
- Location
- 2:28865109
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- start lost
- HGVS.g name
- (GRCh38)2:28865109A>G
- HGVS.c name
- ENSEMBL:ENST00000306108.10:c.710T>C
- ENSEMBL:ENST00000439947.1:n.728T>C
- HGVS.p name
- ENSP00000302801:p.Met237Thr
- XP_016859892:p.Met1?
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:28849821...28870309 (20.49 kb)
- Assembly version
- Not Available
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