Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs223730002
- Species
- Mus musculus
- Symbol
- rs223730002
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30l
- Location
- 11:57694259
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000077.7:g.57694259C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000020826.1:c.198+1144C>T
- RefSeq:NM_001081168.2:c.198+1144C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:57692463...57701043 (8.58 kb)
- Assembly version
- Not Available
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