Allele/Variant

rs3322216506

Species
Rattus norvegicus
Symbol
rs3322216506
Category
Variant
Variant type
SNP
Overlaps
Gltp
Location
12:41912936
Nucleotide Change
A>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (mRatBN7.2)12:41912936A>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000001581.7:c.103+5602A>C
  • RefSeq:NM_001134413.1:c.103+5602A>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
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