Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197166799
- Species
- Rattus norvegicus
- Symbol
- rs197166799
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ubap1
- Location
- 5:56530830
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051340.1:g.56530830G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000096821.1:c.-7-8661G>A
- RefSeq:NM_001012190.1:c.-7-8661G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:56520722...56561153 (40.43 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:ENSRNOT00000096821.1 | protein_coding | Ubap1 | Intron 1/6 |
| ||||
RefSeq:NM_001012190.1 | protein_coding | Ubap1 | Intron 1/6 |
| ||||
RefSeq:XM_008763626.4 | protein_coding | Ubap1 | Intron 1/5 |
| ||||
Showing 1 - 3 of 3 rows
per page