Allele/Variant

rs758449088

Species
Homo sapiens
Symbol
rs758449088
Category
Variant
Variant type
SNP
Overlaps
BRCA1
Location
17:43045705
Nucleotide Change
T>A
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000017.11:g.43045705T>A
HGVS.c name
  • ENSEMBL:ENST00000352993.7:c.2139A>T
  • ENSEMBL:ENST00000461221.5:n.5666A>T
HGVS.p name
  • ENSP00000312236:p.Ile713=
  • ENSP00000417554:p.Ile1853=
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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