Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs239907643
- Species
- Mus musculus
- Symbol
- rs239907643
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wdr55
- Location
- 18:36894659
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)18:36894659T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000049323.1:c.195-371T>C
- RefSeq:NM_026464.3:c.195-371T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:36893275...36896761 (3.49 kb)
- Assembly version
- Not Available
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