Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198343932
- Species
- Rattus norvegicus
- Symbol
- rs198343932
- Category
- Variant
- Variant type
- SNP
- Overlaps
- 6430548M08Rikl
- Location
- 19:48198722
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (mRatBN7.2)19:48198722T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000023478.6:c.105T>C
- ENSEMBL:ENSRNOT00000099058.1:c.105T>C
- HGVS.p name
- ENSRNOP00000023478:p.Asp35=
- ENSRNOP00000077825:p.Asp35=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:48168651...48216575 (47.92 kb)
- Assembly version
- Not Available
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