Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107384658
- Species
- Rattus norvegicus
- Symbol
- rs107384658
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prtfdc1
- Location
- 17:83599301
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051352.1:g.83599301C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000034907.6:c.466-26367G>A
- ENSEMBL:ENSRNOT00000080193.2:c.340-24801G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:83548803...83655179 (106.38 kb)
- Assembly version
- Not Available
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