Allele/Variant

rs8162687

Species
Rattus norvegicus
Symbol
rs8162687
Category
Variant
Variant type
SNP
Overlaps
Pgc
Location
9:13258902
Nucleotide Change
G>A
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_051344.1:g.13258902G>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000019650.4:c.822C>T
  • RefSeq:NM_133284.2:c.822C>T
HGVS.p name
  • ENSRNOP00000019650:p.Gly274=
  • NP_579818:p.Gly274=
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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