Table 2.
Gene | Change | Functional effect | PP | Pathogenicity | MAF in ExAC browse non-Finnish Europeans | No of probands | Dx |
---|---|---|---|---|---|---|---|
CHD7 | c.8962 8963insG p.D2988GfsX2 | Frameshift | NA | Deleterious | Not seen | 1 | nIHH |
CHD7 | c.5051-4C>T | Splice site | NA | Deleterious | Not seen | 1 | KS |
CHD7 | c.101 8A>G p.M340V | Missense | 0/4 | Benign | 0.0063 | 2 | nIHH, KS |
CHD7 | c.7579A>C p.M2527L | Missense | 0/4 | Benign | 0.0031 | 2 | nIHH |
FGFR1 | c.760C>T p.R254W | Missense | 3/4 | Likely deleterious | Not seen | 1 | KS |
FGFR1 | c.1408C>T p.R470C | Missense | 2/4 | Likely deleterious | 0.000015 | 1 | nIHH |
SPRY4 | c.46G>A p.V16I | Missense | 1/4 | Likely benign | 0.0002462 | 1 | KS |
GNRHR | c.436C>T p.P146S | Missense | 3/4 | Likely deleterious | 0.0011 | 1 | nIHH |
GNRHR | c 317A>G p Q106R | Missense | 3/4 | Likely deleterious | 0.003 | 2 | nIHH |
GNRHR | c.785G>A p.R262Q | Missense | 3/4 | Likely deleterious | 0.002 | 1 | nIHH |
GNRHR | c.1-8G>A | Frameshift | NA | Deleterious | Not seen | 1 | nIHH |
KISS1R | c.458C>T p.R153C | Missense | 1/4 | Likely benign | Not seen | 1 | KS |
PROKR2 | c.254G>A p.R85H | Missense | 1/4 | Likely benign | 0.0011 | 1 | KS |
PROKR2 | c.1069C>T p.R357W | Missense | 3/4 | Likely deleterious | 0.00089 | 1 | nIHH |
TACR3 | c.1305T>A p.S435R | Missense | 1/4 | Likely benign | 0.000029 | 1 | nIHH |
ANOS1 | Possible deletion from KAL1 exon1 through Xp22.31 | Intragenic deletion | NA | Deleterious | NA | 2 | KS |
ANOS1 | c.550delC p.L184* | Nonsense | NA | Deleterious | Not seen | 1 | KS |
ANOS1 | c.1 532C>A p.S511Y | Missense | 0/4 | Benign | 0.0024 | 1 | KS |
KL | c.860G>A p.R287H | Missense | 3/4 | Likely deleterious | 0.00001648 | 1 | KS |
POLR3A | c.3734G>A p.R1245Q | Missense | 0/4 | Benign | 0.00283 | 1 | KS |
DMXL2 | c.31 04C>G p.P1035R | Missense | 0/4 | Benign | 0.00004946 | 1 | KS |
DMXL2 | c.1787C>G p.S596C | Missense | 1/4 | Likely benign | 0.0003747 | 1 | KS |
PNPLA6 | c.851 859delinsACCGTGT p.S284YfsX56 | Frameshift | NA | Deleterious | Not seen | 1 | KS |
POLR3B | c.1958A>T p.D653V | Missense | 1/4 | Likely benign | 0.006968 | 1 | nIHH |
POLR3B | c.3358A>G p.M1120V | Missense | 3/4 | Likely deleterious | 0.000008238 | 1 | KS |
RNF216 | c.1 06G>A p.D36N | Missense | 2/4 | Likely deleterious | Not seen | 1 | nIHH |
SPRY4 | c.46G>A p.V16I | Missense | 1/4 | Likely benign | 0.0002822 | 1 | KS |
SOX2 | c. 750 C>A p S250T | Missense | 4/4 | Deleterious | Not seen | 1 | KS |
SOX2 | c. 297 C>A pA99G | Missense | 4/4 | Deleterious | 0.000008347 | 1 | nIHH |
SEMA3A | c.1 457C>T p.P486L | Missense | 2/4 | Likely deleterious | 0.00006603 | 1 | KS |
Table 2 shows the characteristics of the detected RSVs including the genomic changes, function effect, number of prediction programs that consider the changes deleterious, pathogenicity, MAF in ExAC, number of probands carrying the diagnosis and associated diagnosis.