Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs229097600
- Species
- Mus musculus
- Symbol
- rs229097600
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pcdhga3
- Location
- 18:37857695
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)18:37857695C>G
- HGVS.c name
- ENSEMBL:ENSMUST00000073447.1:c.2412+47735C>G
- ENSEMBL:ENSMUST00000115661.1:c.2386-100379C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:37807388...37974926 (167.54 kb)
- Assembly version
- Not Available
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