Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199020117
- Species
- Rattus norvegicus
- Symbol
- rs199020117
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sap30l
- Location
- 10:41982489
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.41982489T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000003473.7:c.199-1347T>C
- RefSeq:NM_001398798.1:c.199-1347T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:41979687...41992307 (12.62 kb)
- Assembly version
- Not Available
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