Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs234629118
- Species
- Mus musculus
- Symbol
- rs234629118
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Tnnt3
- Location
- 7:142066952
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)7:142066952C>G
- HGVS.c name
- ENSEMBL:ENSMUST00000074187.1:c.651+593C>G
- ENSEMBL:ENSMUST00000078497.1:c.711+593C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:142052573...142069746 (17.17 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction