Allele/Variant

rs3321845061

Species
Rattus norvegicus
Symbol
rs3321845061
Category
Variant
Variant type
SNP
Overlaps
Sox9
Location
10:97811902
Nucleotide Change
T>C
Most Severe Consequence
  • 3 prime UTR variant
See all consequences
HGVS.g name
  • NC_051345.1:g.97811902T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000003511.7:c.*2105T>C
  • RefSeq:NM_080403.2:c.*2105T>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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