Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107079669
- Species
- Rattus norvegicus
- Symbol
- rs107079669
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rbbp9
- Location
- 3:131932017
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (mRatBN7.2)3:131932017T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000010678.5:c.78+3A>G
- RefSeq:NM_019219.3:c.81A>G
- HGVS.p name
- NP_062092:p.Val27=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:131925095...131939042 (13.95 kb)
- Assembly version
- Not Available
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