Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs561294281
- Species
- Homo sapiens
- Symbol
- rs561294281
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EXOSC7
- Location
- 3:45007567
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)3:45007567A>T
- HGVS.c name
- ENSEMBL:ENST00000265564.8:c.763A>T
- ENSEMBL:ENST00000461361.5:n.942A>T
- HGVS.p name
- ENSP00000265564:p.Met255Leu
- NP_055819:p.Met255Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:44975241...45036066 (60.83 kb)
- Assembly version
- Not Available
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