Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs259903363
- Species
- Mus musculus
- Symbol
- rs259903363
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Kat14
- Location
- 2:144225086
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:144225086C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000028911.1:c.500+2338C>T
- ENSEMBL:ENSMUST00000130654.1:n.234+2338C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:144210952...144249595 (38.64 kb)
- Assembly version
- Not Available
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