Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3318955138
- Species
- Rattus norvegicus
- Symbol
- rs3318955138
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rpl36l2
- Location
- 1:86062943
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (mRatBN7.2)1:86062943C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000003180.7:c.11G>A
- RefSeq:XM_008759257.4:c.11G>A
- HGVS.p name
- ENSRNOP00000067354:p.Arg4His
- XP_008757479:p.Arg4His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:86062525...86062968 (0.44 kb)
- Assembly version
- Not Available
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