Allele/Variant

rs3320346000

Species
Rattus norvegicus
Symbol
rs3320346000
Category
Variant
Variant type
SNP
Overlaps
Emc3
Location
4:146664091
Nucleotide Change
T>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (mRatBN7.2)4:146664091T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000013488.5:c.761A>G
  • RefSeq:NM_001008355.1:c.761A>G
HGVS.p name
  • ENSRNOP00000013488:p.Lys254Arg
  • NP_001008356:p.Lys254Arg
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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