Allele/Variant

rs3322881547

Species
Rattus norvegicus
Symbol
rs3322881547
Category
Variant
Variant type
SNP
Overlaps
Eif4ebp1
Location
16:64803537
Nucleotide Change
A>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051351.1:g.64803537A>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000016885.6:c.142+2254T>C
  • ENSEMBL:ENSRNOT00000096679.1:c.142+2254T>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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