Allele/Variant

rs3318816910

Species
Rattus norvegicus
Symbol
rs3318816910
Category
Variant
Variant type
SNP
Overlaps
Stxbp5
Location
1:4210319
Nucleotide Change
C>G
Most Severe Consequence
  • 3 prime UTR variant
See all consequences
HGVS.g name
  • (mRatBN7.2)1:4210319C>G
HGVS.c name
  • ENSEMBL:ENSRNOT00000044778.5:c.2150-289G>C
  • ENSEMBL:ENSRNOT00000115103.1:c.2234-289G>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
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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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