Supplementary Table 1



Supplementary Table 1. FUS sequence variations not predicting aminoacid changes identified in ALS patients and/or controls

| |Nucleotide change |Patients |Controls |

|intronic |c.38+11delT |1/338 |nt |

| |c.190+32A>C |1/338 |nt |

| |c.335 -15delTTTT |0/338 |1/621 |

| |c.524-21T>C |2/1009 |2/793 |

| |c.833-29C>T |1/338 |nt |

| |(rs72550862) | | |

| |c.1168+51A>C |1/338 |nt |

| |c.1542-8T>C |0/1009 |1/538 |

| | | | |

|synonymous |c.153C>T |1/338 |nt |

| |(rs61733962) | | |

| |c.675C>T |0/1009 |1/793 |

| |c.1464C>T |2/1009 |1/500 |

| |c.1566G>A |8 /1009 |5/538 |

| | | | |

|3’UTR |c.*41G>A |29/1009 |17/538 |

Only rare variations (Minor Allele Frequency ................
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