Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199287041
- Species
- Rattus norvegicus
- Symbol
- rs199287041
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gpr75
- Location
- 14:104615287
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051349.1:g.104615287G>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000033437.5:c.-99-883G>C
- ENSEMBL:ENSRNOT00000067393.4:c.104+4142G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:104609542...104620370 (10.83 kb)
- Assembly version
- Not Available
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