Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197932302
- Species
- Rattus norvegicus
- Symbol
- rs197932302
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ten1
- Location
- 10:101446482
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:101446482T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000083022.2:c.247+1845T>C
- RefSeq:NM_001108307.1:c.247+1845T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:101431328...101455105 (23.78 kb)
- Assembly version
- Not Available
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