Table 1 Shows the NGS myopathy panel used including the genes for congenital nemaline myopathy

ABHD5, ACADS, ACADVL, ACTA1, ACTN3, ACVR1, AGK, AGL, AGRN, ALG13,  ALG14, ALG2, ANO5, AR, ATP2A1, B3GALNT2, B3GNT1, B4GALNT1, BAG3, BICD2, BIN1,C10orf2, CACNA1A, CACNA1S, CAPN3, CASQ1, CAV3, CCDC78, CFL2, CHAT, CHKB, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CKM, CLCN1, CMYA5, CNBP, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, COLQ, COX15, CPT2, CRYAB, DAG1, DCST2, DES, DMD, DNAJB6, DNM2, DOK7, DOLK, DPAGT1, DPM1, DPM2, DPM3, DYNC1H1, DYSF, ECEL1, EMD, ENO3, ERBB3, ETFA, ETFB, ETFDH, FAM111B, FBN2, FBXO32, FHL1, FHL2, FKBP14, FKRP, FKTN, FLNC, GATM, GBE1, GFPT1, GMPPB, GNB4, GNE, GOSR2, GTDC2, GYG1, GYS1, GAA, HSPB8, HSPG2, IGHMBP2, ISCU, ISPD,  ITGA7, ITPR1, KBTBD13, KCNE1, KCNE3, KCNJ2, KCNQ1, KLHL40, KLHL41, KLHL9, LAMA2, LAMB1, LAMB2, LAMP1, LAMP2, LARGE, LDB3, LDHA, LDHB, LIMS2, LMNA, LMOD3, LPIN1, LRP4,  MATR3, MBNL1, MEGF10, MGME1, MICU1, MSTN, MTM1, MTMR14, MTTP, MUSK, MYBPC1, MYBPC2, MYBPC3, MYF6, MYH14, MYH2, MYH3, MYH4, MYH7, MYH8, MYL1, MYL3, MYLPF, MYOM1, MYOM2, MYOM3, MYOT, MYOZ1, MYOZ2, MYOZ3, MYPN, NBR1, NEB, NEBL, NEFL, NTRK1, OBSL1, OPA1, ORAI1, PABPN1, PDK3, PDLIM3, PDLIM5, PDLIM7, PFKM, PGAM2, PGK1, PGM1, PHKA1, PIP5K1C, PLEC, PLEKHG4, LEKHG5,  PLN, PNPLA2, POLG, POLG2, POMGNT1, POMK, POMT1, POMT2, PREPL, PRKAG2, PTPLA, PTRF, PYGM, RAPSN, RBCK1, RRM2B, RYR1, SCN4A, SEPN1, SGCA, SGCB, SGCD, SGCG, SIL1, SLC22A5, SLC25A20, SLC25A4, SLC52A2, SLC52A3, SLC5A2, SMCHD1, SPEG, QSTM1, SRF, STAC3, STIM1, STIM2, SUCLA2, SYNE1, SYNE2, SYNE3, SYNPO2, TAZ, TCAP, TFG, TIA1, TIAL1, TK2, TMEM43, TMEM5, TMEM55A, TMOD3, TNNC1, TNNC2, TNNI1, TNNI2, NNI3, TNNT1, TNNT3, TNPO3, TNXB, TOR1AIP1, TPM1, TPM2, TPM3, TPP1, TRAPPC1, TRAPPC11, TRIM32, TRIM54, TRIM55, TRIM63, TRPV4, TTC19, TTN, TTR, UBA1, VAPB, VCP, VIPAS39, VMA21, VRK1, YARS2.

Genes associated with congenital nemaline myopathy:

ACTA1, CFL2, KBTBD13, KLH40, KLH41,LMOD3, MYPN, NEB, NEBL,TNNT1, TNNT3, TPM1, TPM2, TPM3