Allele/Variant

rs3321675691

Species
Rattus norvegicus
Symbol
rs3321675691
Category
Variant
Variant type
SNP
Overlaps
Plekhm3
Location
9:66310162
Nucleotide Change
C>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051344.1:g.66310162C>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000032782.7:c.-211-4409G>C
  • RefSeq:XM_006245080.5:c.-123-4497G>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
Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
No records match query. Try removing filters.
Showing 0 - 0 of 0 rows
per page