Allele/Variant

rs106402863

Species
Rattus norvegicus
Symbol
rs106402863
Category
Variant
Variant type
SNP
Overlaps
Prpf38b
Location
2:196555362
Nucleotide Change
C>A
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051337.1:g.196555362C>A
HGVS.c name
  • ENSEMBL:ENSRNOT00000027738.6:c.782+161G>T
  • ENSEMBL:ENSRNOT00000104883.1:c.776+167G>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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