Allele/Variant

rs199096755

Species
Rattus norvegicus
Symbol
rs199096755
Category
Variant
Variant type
SNP
Overlaps
Ube2m
Location
1:73665468
Nucleotide Change
T>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (mRatBN7.2)1:73665468T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000031007.7:c.-969A>G
  • ENSEMBL:ENSRNOT00000108453.1:c.73A>G
HGVS.p name
  • ENSRNOP00000083234:p.Lys25Glu
  • NP_001101941:p.Lys25Glu
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