Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs587777098
- Species
- Homo sapiens
- Symbol
- rs587777098
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNC2I2
- Location
- 9:128634291
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000009.12:g.128634291T>C
- HGVS.c name
- ENSEMBL:ENST00000372715.7:c.1307A>G
- RefSeq:NM_052844.4:c.1307A>G
- HGVS.p name
- ENSP00000361800:p.Lys436Arg
- NP_443076:p.Lys436Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:128633653...128684460 (50.81 kb)
- Assembly version
- Not Available
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