Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106627742
- Species
- Rattus norvegicus
- Symbol
- rs106627742
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Gmfb
- Location
- 15:20073731
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)15:20073731G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000075602.3:c.152-36C>T
- ENSEMBL:ENSRNOT00000101993.1:c.201-67C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:20067263...20081005 (13.74 kb)
- Assembly version
- Not Available
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