Allele/Variant

rs558041696

Species
Homo sapiens
Symbol
rs558041696
Category
Variant
Variant type
SNP
Overlaps
DUSP12
Location
1:161756789
Nucleotide Change
C>T
Most Severe Consequence
  • non coding transcript exon variant
See all consequences
HGVS.g name
  • NC_000001.11:g.161756789C>T
HGVS.c name
  • ENSEMBL:ENST00000367943.5:c.865C>T
  • ENSEMBL:ENST00000484291.5:n.803C>T
HGVS.p name
  • ENSP00000356920:p.Leu289Phe
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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