Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105688538
- Species
- Rattus norvegicus
- Symbol
- rs105688538
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Unc5b
- Location
- 20:28701564
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)20:28701564T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000038537.6:c.2651+322A>G
- RefSeq:NM_022207.2:c.2675+322A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:28697726...28764537 (66.81 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction