ABCC7 p.Pro731Leu
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PMID: 22892530
[PubMed]
Sobczynska-Tomaszewska A et al: "Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy."
No.
Sentence
Comment
56
These newborns had the CFTR genotype as follows: [F508del];[D537N], [F508del];[P731L], [F508del];[T1053I] (two unrelated newborns) and [F508del];[L467F].
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ABCC7 p.Pro731Leu 22892530:56:79
status: NEW57 Mutations D537N and P731L have not been Period of NBS CF Method The most frequent mutations in Polish population under analysis September 2006 - December 2007 Estonia Asper Biotech assay E60X, G85E, 394delTT, R117H, R117P, R117L, I148T, 621G>A, 711+1G>T, 711+5G>A, 1078delT, R334W, R347H, R347P, R347L, IVS8-T, A455E, I507del, F508del, 1717-1G>A, G542X, p.G551D, Q552X, R553X, R553G, R560T, R560K, 1898+1G>A, 1898+1G>T, 1898+1G>C, 2143delT, 2184delA, 2183AA>G, 2789+5G>A, 3120+1G>A, 3199del6, 3272-26A>G, R1162X, 3659delC, 3849+10kbC>T, 3905insT, S1235R, S1251N, W1282X, W1282C, N1303K, CFTRdele2,3 January 2007 - June 2009 Sanger sequencing of exons: 4, 7, 10, 11, 13, 21, fragment of intron 19 F508del, CFTRdele2,3, 3849+10kbC>T, R117H+IVS8-T*, R334W, R347P, 1717-1G>A, G542X, R553X, K710X, 2184insA, 2143delT, 2183AA>G, N1303K July 2009 - currently Sanger sequencing of exons: 7, 10, 11, 13, 17b, 20, 21, fragment of intron 19 F508del, CFTRdele2,3, 3849+10kbC>T, R334W, R347P, 1717-1G>A, G542X, R553X, K710X, 2184insA, 2143delT, 2183AA>G, N1303K, 3272-26A>G**, W1282X** * removed from DNA analysis since July 2009 , **added into DNA analysis since July 2009 Figure 1 NBS CF in Poland.
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ABCC7 p.Pro731Leu 22892530:57:20
status: NEW65 The D537N variant in exon 11 was designated as possibly pathogenic and P731L as possibly tolerated.
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ABCC7 p.Pro731Leu 22892530:65:71
status: NEW106 In example, the detection of a sporadic missense variants (eg, D537N, P731L), still do not provide a clear answer to the biological and clinical significance of the defect.
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ABCC7 p.Pro731Leu 22892530:106:70
status: NEW107 The D537N variant was designated as possibly pathogenic by bioinformatic analysis, whereas the P731L was designated as 'tolerated`.
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ABCC7 p.Pro731Leu 22892530:107:95
status: NEW