Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs773375066
- Species
- Homo sapiens
- Symbol
- rs773375066
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT5
- Location
- 14:60975662
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)14:60975662A>G
- HGVS.c name
- ENSEMBL:ENST00000261249.7:c.1257T>C
- RefSeq:NM_001350253.1:c.1341T>C
- HGVS.p name
- ENSP00000261249:p.Tyr419=
- NP_001337182:p.Tyr447=
- 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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