Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs105068976
- Species
- Rattus norvegicus
- Symbol
- rs105068976
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Avpi1
- Location
- 1:240931911
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)1:240931911C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000019978.4:c.203G>A
- RefSeq:NM_134373.2:c.68G>A
- HGVS.p name
- ENSRNOP00000019978:p.Gly68Asp
- NP_599200:p.Gly23Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:240930236...240936154 (5.92 kb)
- Assembly version
- Not Available
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Data currently unavailable; sequence viewer under construction