Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105630768
- Species
- Rattus norvegicus
- Symbol
- rs105630768
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Matn4
- Location
- 3:153128469
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.153128469G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000018844.7:c.770-830C>T
- ENSEMBL:ENSRNOT00000106259.1:c.650-830C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:153120605...153135865 (15.26 kb)
- Assembly version
- Not Available
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