Allele/Variant

rs3319177646

Species
Rattus norvegicus
Symbol
rs3319177646
Category
Variant
Variant type
SNP
Overlaps
Atg2a
Location
1:203548827
Nucleotide Change
G>A
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_051336.1:g.203548827G>A
HGVS.c name
  • RefSeq:NM_001109545.1:c.1510G>A
  • RefSeq:XR_005492572.2:n.1613G>A
HGVS.p name
  • NP_001103015:p.Gly504Ser
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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