Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3320485621
- Species
- Rattus norvegicus
- Symbol
- rs3320485621
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Pgap4
- Location
- 5:63938115
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)5:63938115G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000008883.8:c.-76+354C>A
- ENSEMBL:ENSRNOT00000104584.1:c.-75-4372C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:63930682...63951716 (21.03 kb)
- Assembly version
- Not Available
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