Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs199409656
- Species
- Rattus norvegicus
- Symbol
- rs199409656
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pgap4
- Location
- 5:63933194
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051340.1:g.63933194A>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000008883.8:c.475T>A
- ENSEMBL:ENSRNOT00000104584.1:c.475T>A
- HGVS.p name
- ENSRNOP00000008883:p.Ser159Thr
- ENSRNOP00000097268:p.Ser159Thr
- 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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