Allele/Variant

rs107323599

Species
Rattus norvegicus
Symbol
rs107323599
Category
Variant
Variant type
SNP
Overlaps
Opa3
Location
1:78887530
Nucleotide Change
C>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)1:78887530C>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000029552.7:c.-352+5936C>G
  • ENSEMBL:ENSRNOT00000096607.1:c.142+5936C>G
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