Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198149876
- Species
- Rattus norvegicus
- Symbol
- rs198149876
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rpl36Al2
- Location
- 1:72505316
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)1:72505316A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000043603.4:c.160A>C
- ENSEMBL:ENSRNOT00000046111.2:c.-311+19698T>G
- HGVS.p name
- ENSRNOP00000048252:p.Thr54Pro
- XP_008757082:p.Thr54Pro
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:72505021...72505474 (0.45 kb)
- Assembly version
- Not Available
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