Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs258912476
- Species
- Mus musculus
- Symbol
- rs258912476
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wdr93
- Location
- 7:79394498
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:79394498C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000035622.1:c.-39+1567C>T
- RefSeq:NM_001037927.1:c.-39+1567C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:79392911...79435698 (42.79 kb)
- Assembly version
- Not Available
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