Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105552662
- Species
- Rattus norvegicus
- Symbol
- rs105552662
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Btg1
- Location
- 7:31341738
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)7:31341738C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000005910.5:c.148+200C>T
- RefSeq:NM_017258.2:c.148+200C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:31341027...31343649 (2.62 kb)
- Assembly version
- Not Available
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