Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs199166445
- Species
- Rattus norvegicus
- Symbol
- rs199166445
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Traf7
- Location
- 10:13540883
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)10:13540883T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000004192.5:c.228+365A>G
- ENSEMBL:ENSRNOT00000097263.1:c.89+365A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:13533570...13552290 (18.72 kb)
- Assembly version
- Not Available
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