Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322374218
- Species
- Rattus norvegicus
- Symbol
- rs3322374218
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Smg7
- Location
- 13:64986984
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)13:64986984C>T
- HGVS.c name
- RefSeq:XM_039090906.2:c.*2720G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:64986145...65050698 (64.55 kb)
- Assembly version
- Not Available
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