Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs107367208
- Species
- Rattus norvegicus
- Symbol
- rs107367208
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 7:24079748
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)7:24079748C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000002638.8:c.1761+463G>A
- ENSEMBL:ENSRNOT00000082016.2:c.1773+463G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:24064404...24117338 (52.93 kb)
- Assembly version
- Not Available
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