Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1205147646
- Species
- Homo sapiens
- Symbol
- rs1205147646
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT5
- Location
- 14:60979829
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000014.9:g.60979829G>A
- HGVS.c name
- ENSEMBL:ENST00000261249.7:c.69C>T
- ENSEMBL:ENST00000553903.1:c.153C>T
- HGVS.p name
- ENSP00000261249:p.Ser23=
- ENSP00000451666:p.Ser50=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction