Allele/Variant

rs199267050

Species
Rattus norvegicus
Symbol
rs199267050
Category
Variant
Variant type
SNP
Overlaps
Nfatc2ip
Location
1:180971675
Nucleotide Change
T>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_051336.1:g.180971675T>C
HGVS.c name
  • ENSEMBL:ENSRNOT00000090200.2:c.52A>G
  • RefSeq:NM_001007692.1:c.52A>G
HGVS.p name
  • ENSRNOP00000073844:p.Ser18Gly
  • NP_001007693:p.Ser18Gly
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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