Allele/Variant
rs3322943085
- Species
- Rattus norvegicus
- Symbol
- rs3322943085
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Eif4ebp1
- Location
- 16:64803088
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)16:64803088C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000016885.6:c.142+2703G>A
- ENSEMBL:ENSRNOT00000096679.1:c.142+2703G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:64790226...64805984 (15.76 kb)
- Assembly version
- Not Available
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