Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs227429029
- Species
- Mus musculus
- Symbol
- rs227429029
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fam98c
- Location
- 7:28853516
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000073.7:g.28853516G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000123416.1:c.339+525C>T
- ENSEMBL:ENSMUST00000134176.1:c.117+328C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:28851935...28855653 (3.72 kb)
- Assembly version
- Not Available
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