Allele/Variant

rs3321728842

Species
Rattus norvegicus
Symbol
rs3321728842
Category
Variant
Variant type
SNP
Overlaps
Clul1
Location
9:113367109
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051344.1:g.113367109C>T
HGVS.c name
  • ENSEMBL:ENSRNOT00000089735.2:c.255+67G>A
  • RefSeq:NM_001033071.1:c.255+67G>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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