Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs8155031
- Species
- Rattus norvegicus
- Symbol
- rs8155031
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Slc3a2
- Location
- 1:205609479
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_051336.1:g.205609479C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000025196.4:c.622G>A
- RefSeq:NM_001271089.2:c.505G>A
- HGVS.p name
- ENSRNOP00000025196:p.Asp208Asn
- NP_001258018:p.Asp169Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:205604468...205618931 (14.46 kb)
- Assembly version
- Not Available
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