Allele/Variant

rs198282694

Species
Rattus norvegicus
Symbol
rs198282694
Category
Variant
Variant type
SNP
Overlaps
Perp
Location
1:13546710
Nucleotide Change
G>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051336.1:g.13546710G>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000016037.7:c.215-4322G>A
  • RefSeq:NM_001106265.2:c.215-4322G>A
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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