Allele/Variant

rs3319683552

Species
Rattus norvegicus
Symbol
rs3319683552
Category
Variant
Variant type
SNP
Overlaps
Lrrc39
Location
2:204521523
Nucleotide Change
C>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051337.1:g.204521523C>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000020297.6:c.114-153C>A
  • RefSeq:NM_001109637.1:c.114-153C>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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