Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs183355161
- Species
- Homo sapiens
- Symbol
- rs183355161
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT5
- Location
- 14:60979684
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)14:60979684A>G
- HGVS.c name
- ENSEMBL:ENST00000261249.7:c.214T>C
- ENSEMBL:ENST00000553903.1:c.298T>C
- HGVS.p name
- ENSP00000261249:p.Leu72=
- ENSP00000451666:p.Leu99=
- 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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