NM_001142571.2:c.758A>G

HGVS Expressions

  • NG_031858.1:g.21576A>G
  • NM_001142571.2:c.758A>G
  • NP_001136043.1:p.Glu253Gly

Associated Genes

RAD51 Paralog D
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Genomic Location

chr17:35103294

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

138873

Epidemiology in the Arab World

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