Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106864347
- Species
- Rattus norvegicus
- Symbol
- rs106864347
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Katnal2
- Location
- 18:70591798
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051353.1:g.70591798A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000048702.7:c.51+15957T>A
- ENSEMBL:ENSRNOT00000117058.1:c.51+15957T>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:70531754...70608082 (76.33 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:ENSRNOT00000048702.7 | protein_coding | Katnal2 | Intron 1/15 |
| ||||
ENSEMBL:ENSRNOT00000117058.1 | protein_coding | Katnal2 | Intron 1/13 |
| ||||
RefSeq:XM_039097298.2 | protein_coding | Katnal2 | Intron 2/16 |
| ||||
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