Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132
1
Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Part of Oslo University Hospital, 0424 Oslo, Norway
2
Center for Hereditary Tumors, HELIOS-Klinikum Wuppertal, University ofWitten-Herdecke, 42283 Wuppertal, Germany
3
Department of Medical Genetics, The Norwegian Radium Hospital, Oslo University Hospital, 0424 Oslo, Norway
4
Center for Bioinformatics, Department of Informatics, University of Oslo, PO box 1080, Blindern, 0316 Oslo, Norway
*
Author to whom correspondence should be addressed.
Cancers 2020, 12(2), 410; https://doi.org/10.3390/cancers12020410
Submission received: 8 January 2020
/
Revised: 6 February 2020
/
Accepted: 6 February 2020
/
Published: 10 February 2020
(This article belongs to the Special Issue BRCA Mutations and Cancer)
The authors wish to make the following corrections to this paper [1]:
The authors would like to replace Table 3 in [1]. The corrections are correcting typographical errors when translating our database in BIC format to HGVS nomenclature, and removing four carriers which had zero follow-up time. The original version of Table 3 is:
and should be replaced with the following Table 3:
The authors would like to apologize for any inconvenience caused to the readers by these changes.
Conflicts of Interest
The authors declare no conflict of interest.
Reference
- Møller, P.; Dominguez-Valentin, M.; Rødland, E.A.; Hovig, E. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Table 3.
Path_BRCA1 variants detected.
| BRCA1 Variant | Number of Carriers |
|---|---|
| c.1016dupA | 366 |
| c.1556delA | 337 |
| c.3228_3229delAG | 193 |
| c.697_698delGT | 159 |
| c.3178G>T | 119 |
| c.4745delA | 63 |
| c.1A>C | 49 |
| c.2351_2357delCGTTACT | 47 |
| c.5075-2A>C | 37 |
| c.3084_3094delTAATAACATTA | 36 |
| c.5047G>T | 35 |
| c.(441 + 1_442–1)_(4357 + 1_4358–1)del | 24 |
| c.(4185 + 1_41861)_(4357 + 1_4358–1)dup | 22 |
| c.3607C>T | 22 |
| c.3048_3052dupTGAGA | 21 |
| c.5266dupC | 20 |
| c.3331_3334delCAAG | 20 |
| c.(5332 + 1_5333–1)_(5406 + 1_5407–1)del | 19 |
| c.1072delC | 18 |
| c.5511G>A | 15 |
| c.1450G>T | 14 |
| c.(80 + 1_81–1)_(4986 + 1_4987–1)del | 12 |
| c.5513T>G | 12 |
| c.66dupA | 12 |
| c.2475delC | 11 |
| c.3966delA | 11 |
| c.2869C>T | 10 |
| c.2591C>G | 10 |
| c.1058G>A | 10 |
| c.3319G>T | 10 |
| c.4065_4068delTCAA | 9 |
| c.5407-25T>A | 8 |
| c.1292dupT | 7 |
| c.2558ins356 | 7 |
| c.3874delT | 6 |
| c.68_69delAG | 6 |
| c.5251C>T | 6 |
| c.5534C>A | 5 |
| c.1687C>T | 5 |
| c.(?_1–1)_(4357 + 1_4358–1)del | 5 |
| c.794_795delCT | 5 |
| c.5503C>T | 5 |
| c.3710delT | 5 |
| c.4035delA | 4 |
| c.2989_2990dupAA | 4 |
| c.4689C>G | 4 |
| c.3319G>T | 4 |
| c.5213G>A | 4 |
| c.4300_4301delA | 4 |
| c.115T>G | 4 |
| c.5153G>C | 3 |
| c.848T>A | 3 |
| c.339_361dup | 3 |
| c.4612C>T | 3 |
| c.(?_1–1)_(134 + 1_135–1)del | 3 |
| c.457_458ins21 | 3 |
| c.3770_3771delAG | 3 |
| c.2869C>T | 3 |
| c.3700_3704delGTAAA | 2 |
| c.3477_3479delAAAinsC | 2 |
| c.3835_3835delG | 2 |
| c.2438dupG | 2 |
| c.2389G>T | 2 |
| c.1695dupG | 2 |
| c.65T>C | 2 |
| c.1287_1287delA | 2 |
| c.385_385delG | 2 |
| c.2681_2682delAA | 2 |
| c.4932_4933dupAA | 2 |
| c.4972_4972delA | 2 |
| c.(5074 + 1_5075–1)_(5592 + 1_?-1)del | 2 |
| c.(134 + 1_135–1)_(441 + 1_442–1)del | 2 |
| c.241C>T | 1 |
| c.5434C>G | 1 |
| c.3817C>T | 1 |
| c.2722G>T | 1 |
| (4185 + 1_41861)_(4357 + 1_4358–1)del | 1 |
| c.4883T>C | 1 |
| c.1059G>A | 1 |
| c.5123C>T | 1 |
| c.3937C>T | 1 |
| c.140G>T | 1 |
| c.1961dupA | 1 |
| c.3808T>G | 1 |
| c.(5193 + 1_5194–1)_(5592 + 1_?-1)del | 1 |
| c.514C>T | 1 |
| c.2185G>T | 1 |
| c.4689C>G | 1 |
| c.130T>A | 1 |
| c.4987-16T>G | 1 |
| c.1674_1674dupA | 1 |
| c.2745_2748delTCAA | 1 |
| c.5075A>C | 1 |
| c.(4675 + 1_4676–1)_(4986 + 1_4987–1)del | 1 |
| c.929delA | 1 |
| c.3005delA | 1 |
| c.5212G>A | 1 |
| Sum | 1918 |
Table 3.
Path_BRCA1 variants detected.
| BRCA1 Variant | Number of Carriers |
|---|---|
| c.1016dupA | 366 |
| c.1556delA | 337 |
| c.3228_3229delAG | 193 |
| c.697_698delGT | 159 |
| c.3178G>T | 119 |
| c.4745delA | 63 |
| c.1A>G | 49 |
| c.2351_2357delCGTTACT | 47 |
| c.5075-2A>C | 37 |
| c.3084_3094delTAATAACATTA | 36 |
| c.5047G>T | 35 |
| del exon 8–13 | 24 |
| c.3607C>T | 22 |
| dup exon 13 | 22 |
| c.3048_3052dupTGAGA | 21 |
| c.3331_3334delCAAG | 20 |
| c.5266dupC | 20 |
| del exon 22 | 19 |
| c.1072delC | 18 |
| c.5511G>A | 15 |
| c.1450G>T | 14 |
| c.3319G>T | 14 |
| c.2869C>T | 13 |
| c.5513T>G | 12 |
| c.66dupA | 12 |
| del exon 3-16 | 12 |
| c.2475delC | 11 |
| c.3966delA | 11 |
| c.1058G>A | 10 |
| c.2591C>G | 10 |
| c.4065_4068delTCAA | 9 |
| c.5407-25T>A | 8 |
| c.1292dupT | 7 |
| c.2558ins356 | 7 |
| c.3874delT | 6 |
| c.457_458ins21 | 6 |
| c.5251C>T | 6 |
| c.68_69delAG | 6 |
| c.1687C>T | 5 |
| c.3710delT | 5 |
| c.5503C>T | 5 |
| c.5534delA | 5 |
| c.794_795delCT | 5 |
| del exon 1–13 | 5 |
| c.4689C>G | 5 |
| c.115T>G | 4 |
| c.2989_2990dupAA | 4 |
| c.4035delA | 4 |
| c.4300delA | 4 |
| c.5213G>A | 4 |
| c.3770_3771delAG | 3 |
| c.4612C>T | 3 |
| c.5153G>C | 3 |
| c.848T>A | 3 |
| del exon 1–3 | 3 |
| c.1287delA | 2 |
| c.1695dupG | 2 |
| c.2389G>T | 2 |
| c.2438dupG | 2 |
| c.2681_2682delAA | 2 |
| c.3477_3479delAAAinsC | 2 |
| c.3700_3704delGTAAA | 2 |
| c.3835delG | 2 |
| c.386delG | 2 |
| c.4932_4933dupAA | 2 |
| c.4972delA | 2 |
| c.65T>C | 2 |
| del exon 18–24 | 2 |
| del exon 5–7 | 2 |
| c.1059G>A | 1 |
| c.130T>A | 1 |
| c.140G>T | 1 |
| c.1674dupA | 1 |
| c.1961dupA | 1 |
| c.2185G>T | 1 |
| c.241C>T | 1 |
| c.2722G>T | 1 |
| c.2727_2730delTCAA | 1 |
| c.3005delA | 1 |
| c.3817C>T | 1 |
| c.3937C>T | 1 |
| c.5075A>C | 1 |
| c.514C>T | 1 |
| c.5212G>A | 1 |
| c.5434C>G | 1 |
| c.929delA | 1 |
| del exon 13 | 1 |
| del exon 16 | 1 |
| del exon 20–24 | 1 |
| Sum | 1914 |
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MDPI and ACS Style
Møller, P.; Dominguez-Valentin, M.; Rødland, E.A.; Hovig, E. Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132. Cancers 2020, 12, 410. https://doi.org/10.3390/cancers12020410
AMA Style
Møller P, Dominguez-Valentin M, Rødland EA, Hovig E. Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132. Cancers. 2020; 12(2):410. https://doi.org/10.3390/cancers12020410
Chicago/Turabian StyleMøller, Pål, Mev Dominguez-Valentin, Einar Andreas Rødland, and Eivind Hovig. 2020. "Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132" Cancers 12, no. 2: 410. https://doi.org/10.3390/cancers12020410
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