Allele/Variant

rs199114032

Species
Rattus norvegicus
Symbol
rs199114032
Category
Variant
Variant type
SNP
Overlaps
Kmt2c
Location
4:9705424
Nucleotide Change
A>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_051339.1:g.9705424A>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000093625.2:c.588-1719A>C
  • ENSEMBL:ENSRNOT00000101551.1:c.591-1719A>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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