Table 3.
ID | BAP1 mutation | Metastases | chr 3 | DNA change | Protein change | Predictred effect | Predicted pathogenic effecta | Previously reported mutations in UM | |
---|---|---|---|---|---|---|---|---|---|
UM_44 | germline | yes | monosomy | exon 1 | c.3G>A | p.Met1Ile | misense: start site lost | LP | [36] |
UM_76 | somatic | yes | monosomy | intron 1 | c.38-1G>C | p.? | splicing | P | [36] |
UM_9 | somatic | yes | monosomy | exon 2 | c.40_52del13 | p.Leu14SerfsTer54 | truncating | P | [36] |
UM_1136 | germline | no | monosomy | exon 2 | c.58_59insTG | p.Glu20ValfsTer53 | truncating | P | |
UM_113 | somatic | yes | monosomy | intron 2 | c.67+1G>A | p.? | splicing | P | [27, 36] |
UM_1123 | somatic | yes | monosomy | intron 2 | c.67+2dupT | p.? | splicing | P | |
UM_1080 | somatic | no | monosomy | intron 2/exon 3 | c.68-12_75del20 | p.? | splicing | P | |
UM_802 | somatic | yes | monosomy | intron 2/exon 3 | c.68-16_69del18 | p.? | splicing | P | [36] |
UM_584 | germline | no | monosomy | exon 3 | c.79delG | p.Val27CysfsTer45 | truncating | P | |
UM_17 | somatic | yes | monosomy | exon 3 | c.82C>T | p.Gln28Ter | truncating | P | [36] |
UM_1207 | somatic | no | monosomy | exon 3 | c.91_93delGAG | p.Glu31del | in-frame deletion | LP | |
UM_1133 | germline | no | disomyb | intron 3 | c.122+1G>C | p.? | splicing | P | |
UM_109 | germline | yes | monosomy | intron 3 | c.122+1G>T | p.? | splicing | P | [36] |
UM_75 | somatic | no | monosomy | exon 4 | c.125_145del21 | p.Pro42_Phe48del | in-frame deletion | LP | [36] |
UM_88 | somatic | yes | monosomy | exon 4 | c.145delC | p.Leu49CysfsTer23 | truncating | P | [36] |
UM_877 | somatic | yes | monosomy | exon 4 | c.165_180del16 | p.Arg57SerfsTer10 | truncating | P | |
UM_13 | somatic | yes | disomyb | exon 4 | c.178C>T | p.Arg60Ter | truncating | P | [36, 45] |
UM_62 | somatic | yes | monosomy | exon 4 | c.202_227del26 | p.Asp68CysfsTer3 | truncating | P | [36] |
UM_780 | somatic | yes | monosomy | exon 4/intron 4 | c.234del96 | p.? | splicing | P | |
UM_119 | somatic | yes | monosomy | exon 4 | c.253C>T | p.Gln85Ter | truncating | P | [36] |
UM_106 | somatic | yes | monosomy | exon 4 | c.254A>C | p.Gln85Pro | missense | P | [36] |
UM_1126 | somatic | no | monosomy | exon 5 | c.295_312del18 | p.Val99_Ser104del | in-frame deletion | LP | |
UM_1046 | somatic | no | monosomy | exon5/intron5 | c.370_375+12del18 | p.? | splicing | P | |
UM_1208 | somatic | yes | monosomy | intron 5/exon 6 | c.376-20_383del28 | p.? | splicing | P | |
UM_56 | somatic | yes | monosomy | exon 6 | c.422A>G | p.His141Arg | missense | LP | [36, 46] |
UM_23 | germline | yes | monosomy | intron 6 | c.438-2A>G | p.? | splicing | P | [36] |
UM_11 | somatic | no | disomyb | intron 6 | c.438-2A>G | p.? | splicing | P | |
UM_27 | somatic | yes | monosomy | intron 6 | c.438-2A>G | p.? | splicing | P | |
UM_58 | germline | no | monosomy | exon 7 | c.458_459delCT | p.Pro153ArgfsTer7 | truncating | P | [9, 36] |
UM_114 | somatic | yes | monosomy | exon 7 | c.497_509del13 | p.Glu166ValfsTer17 | truncating | P | [36] |
UM_51 | somatic | no | monosomy | exon 7 | c.506A>C | p.His169Pro | missense | P | [36] |
UM_1118 | somatic | no | monosomy | exon 7 | c.524C>G | p.Pro175Arg | missense | LP | [27] |
UM_1086 | somatic | yes | monosomy | intron 7/exon 8 | c.581-2_591del13 | p.? | splicing | P | |
UM_60 | somatic | yes | monosomy | exon 8 | c.588G>A | p.Trp196Ter | truncating | P | [23, 47] |
UM_1334 | germline | no | mosaic | exon 8 | c.619delC | p.Arg207GlyfsTer24 | truncating | P | |
UM_105 | somatic | yes | monosomy | intron 8 | c.659+1G>A | p.? | splicing | P | [27, 36] |
UM_35 | somatic | yes | monosomy | exon 9 | c.723T>A | p.Tyr241Ter | truncating | P | [36, 48:c.723T>C] |
UM_107 | somatic | yes | monosomy | exon 9 | c.781C>T | p.Gln261Ter | truncating | P | [36, 49] rs772448753c |
UM_46 | somatic | yes | monosomy | exon 10 | c.904_905insT | p.Pro302LeufsTer5 | truncating | P | [36] |
UM_1029 | somatic | yes | monosomy | exon 12 | c.1134_1143del10_insAA | p.Ala379ArgfsTer16 | truncating | P | |
UM_115 | somatic | yes | monosomy | exon 12 | c.1153C>T | p.Arg385Ter | truncating | P | [32, 36, 44, 50] |
UM_55 | somatic | no | monosomy | exon 12 | c.1175_1182delAGCAGTAC | p.Gln392LeufsTer3 | truncating | P | [36] |
UM_863 | somatic | no | monosomy | exon 12 | c.1192G>T | p.Glu398Ter | truncating | P | |
UM_950 | germline | yes | mosaic | exon 12 | c.1203dupT | p.Glu402Ter | truncating | P | |
UM_69 | somatic | yes | monosomy | exon 12 | c.1217_1220delAGGA | p.Glu406ValfsTer23 | truncating | P | [36] |
UM_1333 | germline | no | mosaic | exon 13 | c.1695dupT | p.Glu566Ter | truncating | P | |
UM_48 | somatic | no | monosomy | exon 13 | c.1729G>C | p.Glu577Gln | missense | P | [36] |
UM_61 | somatic | yes | monosomy | exon 14 | c.1881C>G | p.Tyr627Ter | truncating | P | [36] |
UM_74 | germline | no | monosomy | exon 14 | c.1882_1885delTCAC | p.Ser628ProfsTer8 | truncating | P | [29, 36, 51] |
UM_708 | somatic | no | disomyb | intron 14-3'UTR | c.1890+38_2573del | p.Glu631Ter | truncating (3 exon deletion) | P | |
UM_1113 | somatic | yes | monosomy | exon 15 | c.1926_1951del 26 | p.Ile643GlyfsTer12 | truncating | P | |
UM_104 | somatic | yes | monosomy | exon 15 | c.1932_1948deldel17 | p.Asn645GlnfsTer13 | truncating | P | [36] |
UM_804 | somatic | yes | monosomy | exon 16 | c.1986_1989delTGAT | p.Ile662MetfsTer29 | truncating | P | [36] |
UM_108 | somatic | yes | monosomy | exon 16 | c.2015A>G | p.Asp672Gly | missense | LP | [23, 36] |
aPredicted pathogenic effect based on ACMG guidelines [39] P, pathogenic; LP, likely pathogenic
bindicates UM with chromosome 3 disomy and carrying a germline or somatic BAP1 mutation
**Population frequency rs772448753: 8.2E-06