Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs45823990
- Species
- Mus musculus
- Symbol
- rs45823990
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Cacng7
- Location
- 7:3415194
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:3415194T>C
- HGVS.c name
- ENSEMBL:ENSMUST00000092891.1:c.571-13T>C
- RefSeq:NM_001420208.1:c.571-13T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:3381471...3416737 (35.27 kb)
- Assembly version
- Not Available
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