Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs773909069
- Species
- Homo sapiens
- Symbol
- rs773909069
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CGNL1
- Location
- 15:57546184
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000015.10:g.57546184A>G
- HGVS.c name
- ENSEMBL:ENST00000281282.6:c.3718A>G
- RefSeq:XM_017022686.2:c.3718A>G
- HGVS.p name
- ENSP00000281282:p.Met1240Val
- XP_016878175:p.Met1240Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:57375967...57550717 (174.75 kb)
- Assembly version
- Not Available
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