Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs265028152
- Species
- Mus musculus
- Symbol
- rs265028152
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Mbnl1
- Location
- 3:60438452
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)3:60438452A>C
- HGVS.c name
- ENSEMBL:ENSMUST00000099087.1:c.174+1227A>C
- ENSEMBL:ENSMUST00000191638.1:n.187+29608A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:60380251...60537171 (156.92 kb)
- Assembly version
- Not Available
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