Allele/Variant

rs3318805731

Species
Rattus norvegicus
Symbol
rs3318805731
Category
Variant
Variant type
SNP
Overlaps
Ten1
Location
10:101437843
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051345.1:g.101437843T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000083022.2:c.-46-5711T>C
  • RefSeq:NM_001108307.1:c.-46-5711T>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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