Allele/Variant

rs938522132

Species
Homo sapiens
Symbol
rs938522132
Category
Variant
Variant type
SNP
Overlaps
HIPK3
Location
11:33287358
Nucleotide Change
G>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_000011.10:g.33287358G>C
HGVS.c name
  • ENSEMBL:ENST00000303296.9:c.944G>C
  • ENSEMBL:ENST00000379016.7:c.944G>C
HGVS.p name
  • ENSP00000304226:p.Ser315Thr
  • ENSP00000368301:p.Ser315Thr
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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