Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107361008
- Species
- Rattus norvegicus
- Symbol
- rs107361008
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Unc5b
- Location
- 20:28717662
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)20:28717662G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000038537.6:c.56C>T
- RefSeq:NM_022207.2:c.83-422C>T
- HGVS.p name
- ENSRNOP00000034951:p.Ser19Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:28697726...28764537 (66.81 kb)
- Assembly version
- Not Available
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