Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs198894992
- Species
- Rattus norvegicus
- Symbol
- rs198894992
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Matn4
- Location
- 3:153129502
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.153129502A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000018844.7:c.769+1009T>G
- ENSEMBL:ENSRNOT00000101725.1:c.650-1863T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:153120605...153135865 (15.26 kb)
- Assembly version
- Not Available
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