Table 3.
S. no. | Name | Gene(s) | Condition(s) | Clinical significance (Last reviewed) | GRCh37 | GRCh38 | Variation ID | Allele ID(s) | ||
---|---|---|---|---|---|---|---|---|---|---|
Chromosome | Location | Chromosome | Location | |||||||
1 | NM_000526.4(KRT14):c.1264G > A (p.Glu422Lys) | KRT14 | EBH-DM | Pathogenic (Apr 1, 2000) | 17 | 39739497 | 17 | 41583245 | 14623 | 29662 |
2 | NM_000526.4(KRT14):c.1256T > A (p.Leu419Gln) | KRT14 | EBH-DM | Pathogenic (Apr 1, 2000) | 17 | 39739505 | 17 | 41583253 | 14622 | 29661 |
3 | NM_000526.4(KRT14):c.1243T > C (p.Tyr415His) | KRT14 | EBH-DM | Pathogenic (Mar 27, 2015) | 17 | 39739518 | 17 | 41583266 | 14621 | 29660 |
4 | NM_000526.4(KRT14):c.1237G > A (p.Ala413Thr) | KRT 14 | Not provided | Pathogenic (Jul 31, 2012) | 17 | 39739524 | 17 | 41583272 | 66319 | 77216 |
5 | NM_000526.4(KRT14):c.1234A > T (p.Ile412Phe) | KRT14 | Not provided | Pathogenic (Apr 2, 2018) | 17 | 39739527 | 17 | 41583275 | 66317 | 77214 |
6 | NM_000526.4(KRT14):c.1228C > T (p.Gln410Ter) | KRT14 | Not provided | Pathogenic (Sep 15, 2016) | 17 | 39739533 | 17 | 41583281 | 66313 | 77210 |
7 | NM_000526.4(KRT14):c.1162C > T (p.Arg388Cys) | KRT14 | Not provided | Pathogenic (Oct 13, 2017) | 17 | 39739599 | 17 | 41583347 | 66306 | 77203 |
8 | NM_000526.4(KRT14):c.1151T > C (p.Leu384Pro) | KRT14 | EBS, Koebner type | Pathogenic (Nov 22, 1991) | 17 | 39739610 | 17 | 41583358 | 14611 | 29650 |
9 | NM_000526.4(KRT14):c.442C > T (p.Arg148Cys) | KRT14 | EBS, Koebner type | Pathogenic (Apr 2, 2018) | 17 | 39742645 | 17 | 41586393 | 66368 | 77265 |
10 | NM_000526.4(KRT14):c.374G > A (p.Arg125His) | KRT14 | EBH-DM | Pathogenic (Oct 30, 2017) | 17 | 39742713 | 17 | 41586461 | 14613 | 29652 |
11 | NM_000526.4(KRT14):c.357G > A (p.Met119Ile) | KRT14 | EBS, autosomal recessive | Pathogenic (Sep 1, 1997) | 17 | 39742730 | 17 | 41586478 | 14620 | 29659 |
12 | NM_000421.3(KRT10):c.1374-2A > C | KRT10 | Not provided | Pathogenic (Nov 25, 2015) | 17 | 38975415 | 17 | 40819163 | 449615 | 445767 |
13 | NM_000421.3(KRT10):c.1374-2A > G | KRT10 | EI, congenital reticular | Pathogenic (Oct 1, 2010) | 17 | 38975415 | 17 | 40819163 | 14581 | 29620 |
14 | NM_000421.3(KRT10):c.1373 + 2T > C | KRT10 | Not provided | Pathogenic (May 9, 2017) | 17 | 38975767 | 17 | 40819515 | 432261 | 426219 |
15 | NM_000421.3(KRT10):c.1373 + 1G > A | KRT10 | EI, congenital reticular | Pathogenic (Oct 1, 2010) | 17 | 38975768 | 17 | 40819516 | 14582 | 29621 |
16 | NM_000421.3(KRT10):c.1325T > A (p.Leu442Gln) | KRT10 | BIE | Pathogenic (Feb 1, 1994) | 17 | 38975817 | 17 | 40819565 | 14575 | 29614 |
17 | NM_000421.3(KRT10):c.1300C > T (p.Gln434Ter) | KRT10 | BIE | Pathogenic (Apr 1, 2006) | 17 | 38975842 | 17 | 40819590 | 29764 | 38719 |
18 | NM_000421.3(KRT10):c.1281C > A (p.Cys427Ter) | KRT10 | BIE | Pathogenic (Jul 1, 2008) | 17 | 38975861 | 17 | 40819609 | 29765 | 38720 |
19 | NM_000421.3(KRT10):c.494G > C (p.Arg165Pro) | KRT10 | Not provided | Likely pathogenic (Sep 1, 2016) | 17 | 38978344 | 17 | 40822092 | 432167 | 426220 |
20 | NM_000421.3(KRT10):c.482T > C (p.Leu161Ser) | KRT10 | BIE | Pathogenic (Aug 21, 1992) | 17 | 38978356 | 17 | 40822104 | 14569 | 29608 |
21 | NM_000421.3(KRT10):c.479A > C (p.Tyr160Ser) | KRT10 | Not provided | Pathogenic (Apr 2, 2018) | 17 | 38978359 | 17 | 40822107 | 66178 | 77075 |
22 | NM_000421.3(KRT10):c.478T > G (p.Tyr160Asp) | KRT10 | BIE | Pathogenic (Feb 1, 1994) | 17 | 38978360 | 17 | 40822108 | 14572 | 29611 |
23 | NM_000421.3(KRT10):c.467G > A (p.Arg156His) | KRT10 | BIE | Pathogenic (Sep 20, 2017) | 17 | 38978371 | 17 | 40822119 | 14573 | 29612 |
24 | NM_000421.3(KRT10):c.460A > C (p.Asn154His) | KRT10 | BIE | Pathogenic (Feb 1, 1994) | 17 | 38978378 | 17 | 40822126 | 14571 | 29610 |
EBH-DM epidermolysis bullosa herpetiformis-Dowling Meara, EBS epidermolysis bullosa simplex, EI erythroderma ichthyosiform, BIE Bullous ichthyosiform erythroderma
Italicized words indicate comparison of identical mutation obtained in our study (psoriasis) with other skin disease