Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs197467385
- Species
- Rattus norvegicus
- Symbol
- rs197467385
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Traf7
- Location
- 10:13542583
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051345.1:g.13542583T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000004192.5:c.136+736A>G
- ENSEMBL:ENSRNOT00000097263.1:c.-7+736A>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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