Allele/Variant

rs198042098

Species
Rattus norvegicus
Symbol
rs198042098
Category
Variant
Variant type
SNP
Overlaps
Rxra
Location
3:11070146
Nucleotide Change
G>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051338.1:g.11070146G>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000012892.5:c.1150+284G>C
  • ENSEMBL:ENSRNOT00000099288.1:c.1240+284G>C
HGVS.p name
Not Available
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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