Table 2.
Base pair location in hg19 | Variant type | Nucleotide change | Protein change | phylop | 1-sift | PolyPhen2 | Grantham score | dbSNP137 | Frequency in 1KG Project | Casesa genotypes (homozygous reference allele, heterozygous, homozygous alternative allele) | Controlsb genotypes (homozygous reference allele, heterozygous, homozygous alternative allele) | MAF within combined cases and controls cohort |
---|---|---|---|---|---|---|---|---|---|---|---|---|
31779233 | ifd | c.515_517del | p.Leu172del | . | . | . | . | . | . | 135,1,0 | 106,0,0 | 0.0020c |
31778076 | ns | c.1674A > T | p.Glu558Asp | 0.108385 | T | B | C | . | 0.0000089e | 135,1,0 | 106,0,0 | 0.0020c |
31779521 | ns | c.229G > A | p.Gly77Ser | 0.936178 | D | D | MC | rs368138379 | 0.0000770d | 135,1,0 | 106,0,0 | 0.0020c |
31778948 | ns | c.802G > A | p.Ala268Thr | 0.997482 | D | D | MC | rs34620296 | 0.0014000 | 134,2,0 | 106,0,0 | 0.0041c |
31778950 | ns | c.800C > T | p.Thr267Ile | 0.998993 | D | D | MC | rs139868987 | 0.0014000 | 135,1,0 | 106,0,0 | 0.0020c |
31779728 | ns | c.22G > C | p.Ala8Pro | 0.995889 | D | D | C | rs9469057 | 0.0130000 | 136,0,0 | 103,3,0 | 0.0061 |
31778077 | ns | c.1673A > C | p.Glu558Ala | 0.995982 | T | P | MR | rs2227955 | 0.0480000 | 129,7,0 | 98,8,0 | 0.0309 |
31777946 | ns | c.1804G > A | p.Glu602Lys | 0.997651 | D | B | MC | rs2075800 | 0.2900000 | 57,57,22 | 48,49,9 | 0.3471 |
31778272 | ns | c.1478C > T | p.Thr493Met | 0.008994 | T | B | MC | rs2227956 | 0.8800000 | 6,33,97 | 2,23,81 | 0.1487 |
31778697 | sn | c.1053G > C | p.Leu351Leu | . | . | . | . | rs199780750 | 0.0000400e | 135,1,0 | 106,0,0 | 0.0020 |
31779003 | sn | c.747G > A | p.Arg249Arg | . | . | . | . | rs116768554 | 0.0027000 | 135,1,0 | 106,0,0 | 0.0020 |
31778322 | sn | c.1428C > T | p.Ile476Ile | . | . | . | . | rs35347921 | 0.0040000 | 135,1,0 | 106,0,0 | 0.0020 |
31778831 | sn | c.919 T > C | p.Leu307Leu | . | . | . | . | rs35326839 | 0.0200000 | 133,3,0 | 102,4,0 | 0.0144 |
31778529 | sn | c.1221G > A | p.Thr407Thr | . | . | . | . | rs2075799 | 0.1400000 | 123,13,0 | 90,14,2 | 0.0640 |
14 variants ordered by variant type and within type ordered by frequency in 1000 Genome Project
aSoton PIBD exomes, n = 136
bSoton controls, n = 106
cVariants used in the SKAT-O test
dFrequency in NHLBI ESP
eFrequency in ExAC Browser
Dots denote missing data
ns non-synonymous, sn synonymous, ifd in-frame deletion
B benign, C conservative, D deleterious, MC moderately conservative, MR moderately radical, P possibly damaging, T tolerated