Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs215828607
- Species
- Mus musculus
- Symbol
- rs215828607
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fam107b
- Location
- 2:3624181
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:3624181T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000115052.1:c.-49+9206T>C
- ENSEMBL:ENSMUST00000226435.1:c.415-25084T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:3705049...3783179 (78.13 kb)
- Assembly version
- Not Available
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