Allele/Variant

rs8152970

Species
Rattus norvegicus
Symbol
rs8152970
Category
Variant
Variant type
SNP
Overlaps
Tnfsf13
Location
10:54400060
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)10:54400060C>T
HGVS.c name
  • RefSeq:NM_001009623.2:c.*651G>A
  • RefSeq:XM_008767796.4:c.*365G>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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