Allele/Variant

rs3318946483

Species
Rattus norvegicus
Symbol
rs3318946483
Category
Variant
Variant type
SNP
Overlaps
Opa3
Location
1:78886328
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051336.1:g.78886328T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000029552.7:c.-352+4734T>C
  • ENSEMBL:ENSRNOT00000096607.1:c.142+4734T>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
Viewer Help
78.880M78.885M78.890M78.895M78.900M78.905M78.910M

Variant Molecular Consequences