Allele/Variant

rs431825417

Species
Homo sapiens
Symbol
rs431825417
Category
Variant
Variant type
SNP
Overlaps
BRCA1
Location
17:43047640
Nucleotide Change
T>A
Most Severe Consequence
  • splice region variant&intron variant
See all consequences
HGVS.g name
  • NC_000017.11:g.43047640T>A
HGVS.c name
  • ENSEMBL:ENST00000352993.7:c.2041+3A>T
  • ENSEMBL:ENST00000461221.5:n.5568+3A>T
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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