Version: 8.0.0
Date: Tue Jan 28 2025
rs756112106
Variant overlaps TSPAN18
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs756112106

Species
Homo sapiens
Symbol
rs756112106
Category
Variant
Variant type
SNP
Overlaps
TSPAN18
Location
11:44926750
Nucleotide Change
C>T
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)11:44926750C>T
HGVS.c name
  • ENSEMBL:ENST00000340160.7:c.692C>T
  • ENSEMBL:ENST00000354556.8:n.778+10053G>A
HGVS.p name
  • ENSP00000339820:p.Ala231Val
  • ENSP00000429020:p.Gly234=
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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