Allele/Variant

rs3320838772

Species
Rattus norvegicus
Symbol
rs3320838772
Category
Variant
Variant type
SNP
Overlaps
Scyl2
Location
7:24078017
Nucleotide Change
G>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)7:24078017G>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000119175.1:c.1774-1045C>T
  • RefSeq:NM_001191780.1:c.1762-1045C>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

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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