Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs107016957
- Species
- Rattus norvegicus
- Symbol
- rs107016957
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rmdn1
- Location
- 5:33078370
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.33078370C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000036050.5:c.247+2586C>T
- ENSEMBL:ENSRNOT00000092054.2:c.247+2586C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:33070265...33127328 (57.06 kb)
- Assembly version
- Not Available
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