Allele/Variant

rs3321896747

Species
Rattus norvegicus
Symbol
rs3321896747
Category
Variant
Variant type
SNP
Overlaps
Grk3
Location
12:43639716
Nucleotide Change
G>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051347.1:g.43639716G>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000082322.2:c.113+14704G>A
  • ENSEMBL:ENSRNOT00000082593.2:c.113+14704G>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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