Allele/Variant

rs197132890

Species
Rattus norvegicus
Symbol
rs197132890
Category
Variant
Variant type
SNP
Overlaps
Cmpk2
Location
6:43080045
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051341.1:g.43080045C>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000052003.6:c.992+513C>T
  • RefSeq:NM_001108017.1:c.902+513C>T
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