Allele/Variant

rs197839116

Species
Rattus norvegicus
Symbol
rs197839116
Category
Variant
Variant type
SNP
Overlaps
Mansc4
Location
4:179992484
Nucleotide Change
T>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_051339.1:g.179992484T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000055463.2:c.481A>G
  • RefSeq:XM_001077890.8:c.481A>G
HGVS.p name
  • ENSRNOP00000052329:p.Ile161Val
  • XP_001077890:p.Ile161Val
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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