Allele/Variant

rs107290178

Species
Rattus norvegicus
Symbol
rs107290178
Category
Variant
Variant type
SNP
Overlaps
Nol8
Location
17:14995866
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051352.1:g.14995866T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000073035.2:c.2880-110A>G
  • ENSEMBL:ENSRNOT00000093381.2:c.2898-110A>G
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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