Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs49918283
- Species
- Mus musculus
- Symbol
- rs49918283
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Epcip
- Location
- 16:90865826
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000082.7:g.90865826T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000035689.1:c.-259+94A>G
- ENSEMBL:ENSMUST00000114076.1:c.-11+94A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:90841534...90866040 (24.51 kb)
- Assembly version
- Not Available
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