Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106512890
- Species
- Rattus norvegicus
- Symbol
- rs106512890
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Scyl2
- Location
- 7:24110895
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)7:24110895T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000119175.1:c.-28-4602A>G
- RefSeq:NM_001191780.1:c.-28-4602A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:24064404...24117338 (52.93 kb)
- Assembly version
- Not Available
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