Allele/Variant

rs1026273725

Species
Homo sapiens
Symbol
rs1026273725
Category
Variant
Variant type
SNP
Overlaps
BRCA2
Location
13:32315507
Nucleotide Change
C>G
Most Severe Consequence
  • 5 prime UTR variant
See all consequences
HGVS.g name
  • NC_000013.11:g.32315507C>G
HGVS.c name
  • ENSEMBL:ENST00000530893.7:c.-565C>G
  • ENSEMBL:ENST00000544455.6:c.-40+362C>G
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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