Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3319399791
- Species
- Rattus norvegicus
- Symbol
- rs3319399791
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Brix1
- Location
- 2:59456573
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)2:59456573A>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000024285.7:c.412T>G
- RefSeq:NM_001029915.1:c.312+933T>G
- HGVS.p name
- ENSRNOP00000024285:p.Tyr138Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:59450608...59461495 (10.89 kb)
- Assembly version
- Not Available
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