Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs264047162
- Species
- Mus musculus
- Symbol
- rs264047162
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Mmp28
- Location
- 11:83333562
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)11:83333562C>T
- HGVS.c name
- ENSEMBL:ENSMUST00000021020.1:c.1348G>A
- ENSEMBL:ENSMUST00000103209.1:c.1306G>A
- HGVS.p name
- ENSEMBL:ENSMUSP00000021020:p.Ala450Thr
- ENSEMBL:ENSMUSP00000099498:p.Ala436Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:83331594...83353890 (22.30 kb)
- Assembly version
- Not Available
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