Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106875259
- Species
- Rattus norvegicus
- Symbol
- rs106875259
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tmem218
- Location
- 8:36932422
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)8:36932422T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000012060.7:c.-1-2615T>C
- RefSeq:NM_001008325.1:c.-1-2615T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:36924553...36940564 (16.01 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction