Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319801542
- Species
- Rattus norvegicus
- Symbol
- rs3319801542
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Trub2
- Location
- 3:13039923
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)3:13039923C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000114551.1:c.534-6097G>A
- RefSeq:XM_006233904.5:c.*3286C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:13033745...13059930 (26.19 kb)
- Assembly version
- Not Available
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