Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321405781
- Species
- Rattus norvegicus
- Symbol
- rs3321405781
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rpl36
- Location
- 9:1443637
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)9:1443637C>T
- HGVS.c name
- RefSeq:XM_039084146.2:c.-3+1517C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:98809534...98809897 (0.36 kb)
- Assembly version
- Not Available
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