Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197873779
- Species
- Rattus norvegicus
- Symbol
- rs197873779
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Wars2
- Location
- 2:186500192
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)2:186500192C>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000104876.1:c.91-7486C>A
- ENSEMBL:ENSRNOT00000106687.1:c.91-28894C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:186459444...186543581 (84.14 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction
Variant Molecular Consequences
Sequence feature | Sequence feature type | Associated gene | Location | Molecular consequence | Codon and amino acid change | |||
|---|---|---|---|---|---|---|---|---|
ENSEMBL:ENSRNOT00000104876.1 | protein_coding | Wars2 | Intron 1/5 |
| ||||
ENSEMBL:ENSRNOT00000106687.1 | protein_coding | Wars2 | Intron 1/4 |
| ||||
RefSeq:NM_001168641.1 | protein_coding | Wars2 | Intron 1/5 |
| ||||
RefSeq:XM_039103162.2 | protein_coding | Wars2 | Intron 1/5 |
| ||||
RefSeq:XM_039103163.2 | protein_coding | Wars2 | Intron 1/4 |
| ||||
Showing 1 - 5 of 5 rows
per page