Allele/Variant

rs198453263

Species
Rattus norvegicus
Symbol
rs198453263
Category
Variant
Variant type
SNP
Overlaps
Cul5
Location
8:54025058
Nucleotide Change
A>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051343.1:g.54025058A>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000099521.1:c.2003+114T>C
  • ENSEMBL:ENSRNOT00000114900.1:c.2249+114T>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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