Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105037128
- Species
- Rattus norvegicus
- Symbol
- rs105037128
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gkap1
- Location
- 17:6386979
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051352.1:g.6386979C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000111759.1:c.378+2259C>T
- RefSeq:NM_001012160.1:c.-43+2849C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:6383963...6423684 (39.72 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction