Allele/Variant

rs197232735

Species
Rattus norvegicus
Symbol
rs197232735
Category
Variant
Variant type
SNP
Overlaps
Vasp
Location
1:78911342
Nucleotide Change
A>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)1:78911342A>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000022214.8:c.1039-332T>A
  • ENSEMBL:ENSRNOT00000088676.2:c.967-332T>A
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
78.912M78.914M78.916M78.918M78.920M78.922M78.924M

Variant Molecular Consequences