Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197756622
- Species
- Rattus norvegicus
- Symbol
- rs197756622
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Depdc7
- Location
- 3:91114196
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)3:91114196G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000016677.6:c.74-5887C>G
- ENSEMBL:ENSRNOT00000111299.1:c.35-5887C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:91099111...91121152 (22.04 kb)
- Assembly version
- Not Available
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