Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs587108412
- Species
- Mus musculus
- Symbol
- rs587108412
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ptger2
- Location
- 14:45227965
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000080.7:g.45227965C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000046891.1:c.843+701C>T
- RefSeq:NM_008964.4:c.843+701C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:45225652...45241277 (15.63 kb)
- Assembly version
- Not Available
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