Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198119290
- Species
- Rattus norvegicus
- Symbol
- rs198119290
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tmem39b
- Location
- 5:142028193
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)5:142028193A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000032558.7:c.1116-1807T>G
- ENSEMBL:ENSRNOT00000117815.1:c.1116-1807T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:142024271...142046607 (22.34 kb)
- Assembly version
- Not Available
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