Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs197113221
- Species
- Rattus norvegicus
- Symbol
- rs197113221
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Smg7
- Location
- 13:64988179
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (mRatBN7.2)13:64988179T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000044235.6:c.*1525A>G
- ENSEMBL:ENSRNOT00000092269.2:c.*1525A>G
- 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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