# a | Mutation name b | Base change c | Intron/Exon | Protein change d | Length of the putative protein product | 1st author & year of 1streport [ref.] | Number of cases |
1 | Afula | c.1A>C | E-1 | undefined defect | ? | Caridi-2013 [18] | 2 closely related families |
2 | Baghdad | c.79+1G>A | I-1 | undefined splicing defect | ? | Campagnoli-2002 [4] | 1 |
3 | Madeira | C.138-2A>G | I-2 | undefined splicing defect | ? | Caridi-2018 [22] | 1 |
4 | Codogno | c.166C>T | E-3 | p.Gln56* | 31 | Watkins-1994 [3] | 1 |
5 | Kayseri | c.228_229delAT | E-3 | p.Val78Cysfs*2 | 54 | Galliano-2002 [5] | 14 |
6 | Amasya | c.229_230delTG | E-3 | p.Val78Cysfs*2 | 54 | Caridi-2012 [16] | 1 |
7 | Treves | c.270+1G>T | I-3 | undefined splicing defect | ? | Caridi-2016 [20] | 1 |
8 | Bethesda | c.412C>T | E-4 | p.Arg138* | 113 | Watkins-1994 [3] | 3 (unrelated) |
9 | Erzurum | c.527delC | E-5 | p.Pro176Argfs*65 | 239 | Caridi-2016 [21] | 2 (same family) |
10 | Zonguldak | c.597T>A | E-5 | splicing defect? | ? | Caridi-2008 [9] | 1 |
11 | Nijmegen-2 | c.615G>A | E-5 | undefined splicing defect | ? | Unpublished | 1 |
12 | Vancouver | c.714-2A>G | I-6 | undefined splicing defect | ? | Watkins-1994 [3] | 1 |
13 | Seattle | c.714G>A | E-7 | p.Trp238* | 213 | Rufner-1988 [1] | 1 |
14 | El Jadida | c.802G>T | E-7 | p.Glu268Ter | 243 | Campagnoli – 2005 [6] | 2 unrelated |
15 | Roma | c.872dupA | E-8 | p.Asn291Lysfs*8 | 273 | Watkins-1994 [2] | 2 (same family) |
16 | Bologna | c.920delT | E-8 | p.Leu307Argfs*23 | 304 | Dagnino-2010 [12] | 1 |
17 | Ghazaouet | c.1098dup | E-9 | p.Val367fs*12 | 353 | Caridi – 2019 [23] | 2 (same family) |
18 | Roma-2 | c.1225C>T | E-10 | p.Gln409* | 384 | Campagna-2005 [7] | 1 |
19 | Monastir | c.1275C>A | E-10 | p.Tyr425* | 400 | Caridi-2009 [11] | 1 |
20 | Guimarães | c.1289+1G>A | I- 10 | p.Phe398Alafs*33 | 405 | Caridi-2012 [15] | 5 (2 same family + 3 unrelated) |
21 | Hama | c.1309A>T | E-11 | p. Lys437Ter | 412 | Caridi-2020 [24] | 1 |
22 | Fondi | c.1427A>G | E-11 | p.Tyr476Serfs*13 | 463 | Campagna-2005 [7] | 1 |
23 | Tripoli | c.1428+1 G>T | I-11 | undefined splicing defect | ? | Bibi-2012 [17] | 2 (same family) |
24 | Bartin | c.1428+2T>C | I-11 | p.Leu431Tyrfs*5 | 410 | Dolcini-2007 [8] | 1 |
25 | Tubingen | c.1525C>T | E-12 | p.Arg509* | 484 | Ruhoff-2010 [14] | 2 (same family) |
26 | Locust Valley | c.1610delT | E-12 | p.Ile537Asnfs*21 | 532 | Davis-2008 [10] | 1 |
27 | Safranbolu | c.1614_15delCA | E-12 | p.Leu540Phefs*2 | 516 | Dagnino-2010 [13] | 2 |
28 | Ankara | c.1652+1G>A | I-12 | p.Leu477Cysfs*4 | 479 | Caridi-2014 [19] | 1 |
aThe mutations are ordered on the basis of their positions in the albumin gene
bThe mutations have been named after the place from where the first detected carrier originates. cbp and codon numbering is according to HGVS rules and is based on the cDNA sequence NM_000477.7. dThe protein changes in analbuminemia are deduced from mRNA (Guimarães , Fondi, Bartin and Ankara) or DNA (all the others) sequence and were not established at the protein level. Subtract 24 from amino acid numbers to convert to starting at the Asp1 of mature albumin. |
REVISED 22.01.2021