Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs8160538
- Species
- Rattus norvegicus
- Symbol
- rs8160538
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prb1
- Location
- 4:165509641
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (mRatBN7.2)4:165509641A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000013887.6:c.267T>G
- RefSeq:NM_001395623.1:c.267T>G
- HGVS.p name
- ENSRNOP00000013885:p.Arg89=
- NP_001382552:p.Arg89=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:165508927...165512393 (3.47 kb)
- Assembly version
- Not Available
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