Allele/Variant

rs104981455

Species
Rattus norvegicus
Symbol
rs104981455
Category
Variant
Variant type
SNP
Overlaps
Nol8
Location
17:15013616
Nucleotide Change
C>T
Most Severe Consequence
  • 5 prime UTR variant
See all consequences
HGVS.g name
  • (mRatBN7.2)17:15013616C>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000073035.2:c.-555G>A
  • ENSEMBL:ENSRNOT00000093381.2:c.-555G>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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