NM_000059.4:c.8117A>G

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HGVS Expressions

  • NG_012772.3:g.52840A>G
  • NM_000059.4:c.8117A>G
  • NP_000050.3:p.Asn2706Ser
  • NC_000013.11:g.32363319A>G

Associated Genes

BRCA2 Gene
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

Variant Type

Substitution

dbSNP

80359055

Clinvar

38139

Contributors

  • Pratibha Nair: 24.01.2024

Edit History

  • Pratibha Nair: 24.01.2024
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.