Version: 7.5.0
Date: Fri Dec 13 2024 Allele/Variant
rs766498367
- Species
- Homo sapiens
- Symbol
- rs766498367
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUP210L
- Location
- 1:154094963
- Nucleotide Change
C>T
- Most Severe Consequence
- See all consequences
- HGVS.g name
- HGVS.c name
- ENSEMBL:ENST00000271854.3:c.2159G>A
- ENSEMBL:ENST00000368559.8:c.2159G>A
- HGVS.p name
- ENSP00000271854:p.Arg720Gln
- ENSP00000357547:p.Arg720Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Assembly version
- Not Available
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Variant Molecular Consequences