Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106915065
- Species
- Rattus norvegicus
- Symbol
- rs106915065
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cuedc2
- Location
- 1:245197350
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)1:245197350T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000026609.7:c.-11+2355A>G
- ENSEMBL:ENSRNOT00000097448.1:c.-11+2941A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:245192057...245200594 (8.54 kb)
- Assembly version
- Not Available
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