Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107427578
- Species
- Rattus norvegicus
- Symbol
- rs107427578
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rufy2
- Location
- 20:25649021
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)20:25649021T>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000037409.7:c.404+1004A>C
- ENSEMBL:ENSRNOT00000084720.2:c.398+1004A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:25621999...25658186 (36.19 kb)
- Assembly version
- Not Available
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