Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs31082292
- Species
- Mus musculus
- Symbol
- rs31082292
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Vmn1r88
- Location
- 7:12912217
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)7:12912217A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000171783.1:c.572A>C
- ENSEMBL:ENSMUST00000236472.1:c.572A>C
- HGVS.p name
- ENSEMBL:ENSMUSP00000128946:p.Asp191Ala
- ENSEMBL:ENSMUSP00000158066:p.Asp191Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:12911646...12912596 (0.95 kb)
- Assembly version
- Not Available
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