Allele/Variant

rs105553652

Species
Rattus norvegicus
Symbol
rs105553652
Category
Variant
Variant type
SNP
Overlaps
Stxbp5
Location
1:4283654
Nucleotide Change
C>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051336.1:g.4283654C>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000044778.5:c.434+4058G>T
  • ENSEMBL:ENSRNOT00000115103.1:c.434+4058G>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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