Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106777511
- Species
- Rattus norvegicus
- Symbol
- rs106777511
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Emc3
- Location
- 4:146677448
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051339.1:g.146677448A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000013488.5:c.155+1263T>A
- RefSeq:NM_001008355.1:c.155+1263T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:146663065...146679029 (15.96 kb)
- Assembly version
- Not Available
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