Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs261716069
- Species
- Mus musculus
- Symbol
- rs261716069
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Lsm3
- Location
- 6:91497768
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)6:91497768A>T
- HGVS.c name
- ENSEMBL:ENSMUST00000040607.1:c.228+1142A>T
- ENSEMBL:ENSMUST00000206947.1:c.228+1142A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:91493017...91499602 (6.59 kb)
- Assembly version
- Not Available
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