Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106067436
- Species
- Rattus norvegicus
- Symbol
- rs106067436
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pgap4
- Location
- 5:63932502
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (mRatBN7.2)5:63932502A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000008883.8:c.1167T>G
- ENSEMBL:ENSRNOT00000104584.1:c.1167T>G
- HGVS.p name
- ENSRNOP00000008883:p.Gly389=
- ENSRNOP00000097268:p.Gly389=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:63930682...63951716 (21.03 kb)
- Assembly version
- Not Available
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