Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197473693
- Species
- Rattus norvegicus
- Symbol
- rs197473693
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Noto
- Location
- 4:117962095
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)4:117962095A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000057516.4:c.380-427A>T
- RefSeq:NM_001192014.1:c.380-427A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:117961163...117965402 (4.24 kb)
- Assembly version
- Not Available
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