Allele/Variant

rs1553363925

Species
Homo sapiens
Symbol
rs1553363925
Category
Variant
Variant type
SNP
Overlaps
PRKCE
Location
2:46151104
Nucleotide Change
G>A
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)2:46151104G>A
HGVS.c name
  • ENSEMBL:ENST00000306156.8:c.1795G>A
  • ENSEMBL:ENST00000469753.5:n.882G>A
HGVS.p name
  • ENSP00000306124:p.Glu599Lys
  • NP_005391:p.Arg656Gln
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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