Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198095192
- Species
- Rattus norvegicus
- Symbol
- rs198095192
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Bmp4
- Location
- 15:19627636
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051350.1:g.19627636C>T
- HGVS.c name
- RefSeq:XM_006251751.4:c.-132-5361G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:19618538...19633494 (14.96 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction