Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs105072695
- Species
- Rattus norvegicus
- Symbol
- rs105072695
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Nek7
- Location
- 13:50042422
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)13:50042422T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000000817.7:c.590-3098A>G
- ENSEMBL:ENSRNOT00000090162.2:c.704-3098A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:50022212...50149374 (127.16 kb)
- Assembly version
- Not Available
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