Table 1.
Gene | OMIM/ OMIA number | Variant designationa | Alternative allele frequency | ||
---|---|---|---|---|---|
Genomic position | Coding DNA change | Protein change | |||
ATXN7 | 607640 | chr20:27,234,549 | c.2285 T > C | p.Val762Ala | 0.1154 |
CEP55 | 610000 | chr28:7,777,489 | c.1334A > C | p.Tyr446Ser | 0.0256 |
CNTF | 118945 | chr18:37,758,771 | c.401_402insA | p.Asn137fs | 0.0128 |
ELOVL4 | 605512 | chr12:40,850,011 | c.424_433delGGAGCACAGC | p.Gly142fs | 0.0128 |
FDX1L | 614585 | chr20:50,798,661 | c.124_125insGGCCGCCATCACCACGGCGGTGAGCACCGCCGCCAGCAGCACCAGCCCGTCAGCGTTGAGCCG | p.Thr41_Ala42insGlyProProSerProArgArgTer | 0.0128 |
GJA9b | 611923/2119–9615 | chr15:3,863,519 | c.1108_1109delGA | p.Glu370fs | 0.0513 |
MCM3AP | 603294 | chr31:39,553,337 | c.1785_1793delCTCTGAAGG | p.Ser596_Gly598del | 0.0128 |
NAPEPLDc | 612334/1788–9615 | chr18:16,987,520 | c.559G > C | p.Ala187Pro | 0.1154 |
PLEKHG5 | 611101 | chr5:60,325,903 | c.1585C > T | p.Gln529* | 0.0128 |
SPTBN4 | 606214/2232–9823 | chr1:113,215,064 | c.1247_1248insGGTAGCCCATGCGGT | p.Ala416_Ala417insValAlaHisAlaVal | 0.0128 |
SYNE1 | 608441 | chr1:42,549,994 | c.17359C > T | p.Arg5788Trp | 0.0256 |
aAdditional details including the protein prediction effects are described in Additional file 10 Table S6. All positions refer to the CanFam3.1 reference sequence assembly
bPreviously described polyneuropathy-associated variant [5]
cPreviously described leukoencephalomyelopathy-associated variant [6]