Allele/Variant

rs2050971311

Species
Homo sapiens
Symbol
rs2050971311
Category
Variant
Variant type
SNP
Overlaps
BRCA1
Location
17:43047622
Nucleotide Change
A>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCh38)17:43047622A>T
HGVS.c name
  • ENSEMBL:ENST00000352993.7:c.2041+21T>A
  • ENSEMBL:ENST00000461221.5:n.5568+21T>A
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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