Allele/Variant

rs106312444

Species
Rattus norvegicus
Symbol
rs106312444
Category
Variant
Variant type
SNP
Overlaps
Nol8
Location
17:15002312
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051352.1:g.15002312C>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000073035.2:c.2665+401G>A
  • ENSEMBL:ENSRNOT00000093381.2:c.2683+401G>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
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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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