Allele/Variant

rs1567756588

Species
Homo sapiens
Symbol
rs1567756588
Category
Variant
Variant type
SNP
Overlaps
BRCA1
Location
17:43045752
Nucleotide Change
C>G
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_000017.11:g.43045752C>G
HGVS.c name
  • ENSEMBL:ENST00000352993.7:c.2092G>C
  • ENSEMBL:ENST00000461221.5:n.5619G>C
HGVS.p name
  • ENSP00000312236:p.Asp698His
  • ENSP00000417554:p.Asp1838His
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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