Allele/Variant

rs760655471

Species
Homo sapiens
Symbol
rs760655471
Category
Variant
Variant type
SNP
Overlaps
BRCA2
Location
13:32319099
Nucleotide Change
T>C
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000013.11:g.32319099T>C
HGVS.c name
  • ENSEMBL:ENST00000470094.2:n.289T>C
  • ENSEMBL:ENST00000530893.7:c.-280T>C
HGVS.p name
  • ENSP00000439902:p.Asn30=
  • ENSP00000505508:p.Asn30=
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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