Allele/Variant

rs3322172134

Species
Rattus norvegicus
Symbol
rs3322172134
Category
Variant
Variant type
SNP
Overlaps
Lemd1
Location
13:43684383
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)13:43684383C>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000076457.3:c.203-12912C>T
  • ENSEMBL:ENSRNOT00000080556.2:c.274-11356C>T
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