Allele/Variant

rs3319632697

Species
Rattus norvegicus
Symbol
rs3319632697
Category
Variant
Variant type
SNP
Overlaps
Reg4
Location
2:185833102
Nucleotide Change
G>T
Most Severe Consequence
  • 3 prime UTR variant
See all consequences
HGVS.g name
  • (mRatBN7.2)2:185833102G>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000025821.3:c.*331G>T
  • RefSeq:NM_001004096.2:c.*331G>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
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Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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