Allele/Variant

rs3321726623

Species
Rattus norvegicus
Symbol
rs3321726623
Category
Variant
Variant type
SNP
Overlaps
Clul1
Location
9:113367179
Nucleotide Change
C>G
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (mRatBN7.2)9:113367179C>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000089735.2:c.252G>C
  • RefSeq:NM_001033071.1:c.252G>C
HGVS.p name
  • ENSRNOP00000070864:p.Lys84Asn
  • NP_001028243:p.Lys84Asn
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available

Genome location
Assembly version
Not Available
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Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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