Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321067172
- Species
- Rattus norvegicus
- Symbol
- rs3321067172
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 7:24114934
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051342.1:g.24114934G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000119175.1:c.-29+2140C>G
- RefSeq:NM_001191780.1:c.-29+2140C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:24064404...24117338 (52.93 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction