Version: 8.0.0
Date: Tue Jan 28 2025
rs115173488
Variant overlaps ST3GAL5
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs115173488

Species
Homo sapiens
Symbol
rs115173488
Category
Variant
Variant type
SNP
Overlaps
ST3GAL5
Location
2:85848441
Nucleotide Change
C>G
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCh38)2:85848441C>G
HGVS.c name
  • ENSEMBL:ENST00000306262.10:n.278-237G>C
  • ENSEMBL:ENST00000377332.8:c.319-357G>C
HGVS.p name
Not Available
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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