Version: 8.0.0
Date: Tue Jan 28 2025
rs3319642276
Variant overlaps Lrrc39
Rattus norvegicus
SummaryVariant Molecular Consequences
Allele/Variant

rs3319642276

Species
Rattus norvegicus
Symbol
rs3319642276
Category
Variant
Variant type
SNP
Overlaps
Lrrc39
Location
2:204528158
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)2:204528158T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000020297.6:c.514-122T>C
  • RefSeq:NM_001109637.1:c.514-122T>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
ENSEMBL:ENSRNOT00000020297.6
protein_codingLrrc39Intron 5/8
  • intron variant
RefSeq:NM_001109637.1
protein_codingLrrc39Intron 5/8
  • intron variant
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