Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3322242003
- Species
- Rattus norvegicus
- Symbol
- rs3322242003
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Foxn4
- Location
- 12:42351978
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)12:42351978A>G
- HGVS.c name
- RefSeq:NM_001389259.1:c.386-764A>G
- RefSeq:XM_039089275.2:c.386-764A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:42336706...42359932 (23.23 kb)
- Assembly version
- Not Available
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