Allele/Variant

rs198741167

Species
Rattus norvegicus
Symbol
rs198741167
Category
Variant
Variant type
SNP
Overlaps
Trpv1
Location
10:57856302
Nucleotide Change
C>A
Most Severe Consequence
  • missense variant&splice region variant
See all consequences
HGVS.g name
  • (mRatBN7.2)10:57856302C>A
HGVS.c name
  • RefSeq:NM_031982.1:c.287C>A
HGVS.p name
  • NP_114188:p.Pro96Gln
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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