Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs51669776
- Species
- Mus musculus
- Symbol
- rs51669776
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Prss54
- Location
- 8:96286141
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)8:96286141T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000052690.1:c.931A>G
- ENSEMBL:ENSMUST00000180075.1:c.931A>G
- HGVS.p name
- ENSEMBL:ENSMUSP00000058859:p.Thr311Ala
- ENSEMBL:ENSMUSP00000137577:p.Thr311Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:96285694...96302965 (17.27 kb)
- Assembly version
- Not Available
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