ClinVar Miner

Submissions for variant NM_000132.3(F8):c.5960_5964del (p.Lys1987fs) (rs1569559514)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000756110 SCV000883828 pathogenic not provided 2017-12-28 criteria provided, single submitter clinical testing The F8 c.5960_5964delAAGAG; p.Lys1987fs variant is not published in the medical literature, in gene-specific databases, or in the ClinVar database. However, other deletions in the region are described in the medical literature in individuals with hemophilia A (Nair 2014, Vinciguerra 2006). The c.5960_5964del variant is not listed in the dbSNP variant database or included in the general population-based databases. This variant deletes 5 nucleotides, leading to a frameshift, and is predicted to result in a truncated protein or mRNA subject to non-sense mediated decay. Considering available information, this variant is classified as pathogenic. References: Nair PS et al. Mutations in intron 1 and intron 22 inversion negative haemophilia A patients from Western India. PLoS One. 2014 May 20;9(5):e97337. Vinciguerra C et al. Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France. Description of 62 novel mutations. Thromb Haemost. 2006 Apr;95(4):593-9.

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