Allele/Variant

rs1463374308

Species
Homo sapiens
Symbol
rs1463374308
Category
Variant
Variant type
SNP
Overlaps
DDX3X
Location
X:41343726
Nucleotide Change
T>C
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • NC_000023.11:g.41343726T>C
HGVS.c name
  • ENSEMBL:ENST00000399959.7:c.677-11T>C
  • ENSEMBL:ENST00000441189.4:c.680-11T>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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