Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320810748
- Species
- Rattus norvegicus
- Symbol
- rs3320810748
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wdcp
- Location
- 6:27860035
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051341.1:g.27860035C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000075574.3:c.1821+1062C>T
- ENSEMBL:ENSRNOT00000110968.1:c.1821+1062C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:27850684...27865540 (14.86 kb)
- Assembly version
- Not Available
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