Somatic mutations affecting CHD2 in CLL and MBL patients
Case . | Genomic . | Exon . | Mutation . | AF . | Type . | Prediction . | IGHV status . |
---|---|---|---|---|---|---|---|
CLL | |||||||
7 | 93552555 | 35-36 | — | 0.20-0.52 | Splicing | — | Mutated |
17 | 93467744 | 3 | p.P86A | 0.40-0.59 | Missense | Neutral | Unmutated |
43 | 93540558 | 30 | p.L1270F | 0.23-0.50 | Missense | Deleterious | Mutated |
175 | 93510647 | 17 | p.L698Gfs*35 | 0.32-0.57 | Deletion | — | Mutated |
181 | 93534730 | 27 | p.F1146L | 0.37-0.64 | Missense | Deleterious | Mutated |
185 | 93499738 | 16 | p.H620L | 0.39-0.64 | Missense | Deleterious | Mutated |
274 | 93522456 | 22 | p.I940Gfs*21 | 0.12-0.29 | Deletion | — | Mutated |
381 | 93514997 | 18 | p.W731* | 0.26-0.48 | Nonsense | — | Mutated |
569 | 93521534 | 21 | p.V883D | 0.38-0.55 | Missense | Deleterious | Mutated |
591 | 93521549 | 21 | p.D888V | 0.42-0.67 | Missense | Deleterious | Mutated |
709 | 93536130 | 28 | p.S1166del | 0.16-0.43 | Deletion | — | Mutated |
723 | 93545499 | 33 | p.D1410Kfs*65 | 0.35-0.58 | Deletion | — | Unmutated |
767 | 93540618 | 30 | p.L1290Nfs*2 | 0.30-0.50 | Deletion | — | Mutated |
788 | 93552392 | 35 | p.R1477Pfs*13 | 0.35-0.68 | Insertion | — | Mutated |
853 | 93485082 | 8 | p.D241Dfs*3 | 0.23-0.52 | Insertion | — | Unmutated |
880 | 93540545 | 30 | p.D1266V | 0.13-0.28 | Missense | Deleterious | Mutated |
1162 | 93540578 | 30 | p.G1277V | 0.09-0.46 | Missense | Deleterious | Mutated |
1177 | 93541759 | 31 | p.Q1306Rfs*55 | 0.16-0.70 | Deletion | — | Mutated |
1191 | 93540226 | 29 | p.I1212T | 0.29-0.63 | Missense | Deleterious | Mutated |
1192 | 93499759 | 16 | p.S627F | 0.14-0.43 | Missense | Deleterious | Unmutated |
1343 | 93487716 | 10 | p.K375Kfs*5 | 0.26-0.56 | Insertion | — | Mutated |
1424 | 93510649 | 17 | p.R699W | 0.31-0.64 | Missense | Deleterious | Mutated |
1431 | 93510649 | 17 | p.R699W | 0.46-0.77 | Missense | Deleterious | Unmutated |
1535 | 93552489 | 35 | p.G1510R | 0.21-0.65 | Missense | Deleterious | Mutated |
MBL | |||||||
152 | 93444511 | 2 | p.L15Hfs*79 | 0.24-0.71 | Insertion | — | — |
190 | 93487649 | 10 | p.G353W | 0.09-0.48 | Missense | Neutral | — |
383 | 93524650 | 24 | p.T1011Nfs*6 | 0.19-0.44 | Insertion | — | — |
Case . | Genomic . | Exon . | Mutation . | AF . | Type . | Prediction . | IGHV status . |
---|---|---|---|---|---|---|---|
CLL | |||||||
7 | 93552555 | 35-36 | — | 0.20-0.52 | Splicing | — | Mutated |
17 | 93467744 | 3 | p.P86A | 0.40-0.59 | Missense | Neutral | Unmutated |
43 | 93540558 | 30 | p.L1270F | 0.23-0.50 | Missense | Deleterious | Mutated |
175 | 93510647 | 17 | p.L698Gfs*35 | 0.32-0.57 | Deletion | — | Mutated |
181 | 93534730 | 27 | p.F1146L | 0.37-0.64 | Missense | Deleterious | Mutated |
185 | 93499738 | 16 | p.H620L | 0.39-0.64 | Missense | Deleterious | Mutated |
274 | 93522456 | 22 | p.I940Gfs*21 | 0.12-0.29 | Deletion | — | Mutated |
381 | 93514997 | 18 | p.W731* | 0.26-0.48 | Nonsense | — | Mutated |
569 | 93521534 | 21 | p.V883D | 0.38-0.55 | Missense | Deleterious | Mutated |
591 | 93521549 | 21 | p.D888V | 0.42-0.67 | Missense | Deleterious | Mutated |
709 | 93536130 | 28 | p.S1166del | 0.16-0.43 | Deletion | — | Mutated |
723 | 93545499 | 33 | p.D1410Kfs*65 | 0.35-0.58 | Deletion | — | Unmutated |
767 | 93540618 | 30 | p.L1290Nfs*2 | 0.30-0.50 | Deletion | — | Mutated |
788 | 93552392 | 35 | p.R1477Pfs*13 | 0.35-0.68 | Insertion | — | Mutated |
853 | 93485082 | 8 | p.D241Dfs*3 | 0.23-0.52 | Insertion | — | Unmutated |
880 | 93540545 | 30 | p.D1266V | 0.13-0.28 | Missense | Deleterious | Mutated |
1162 | 93540578 | 30 | p.G1277V | 0.09-0.46 | Missense | Deleterious | Mutated |
1177 | 93541759 | 31 | p.Q1306Rfs*55 | 0.16-0.70 | Deletion | — | Mutated |
1191 | 93540226 | 29 | p.I1212T | 0.29-0.63 | Missense | Deleterious | Mutated |
1192 | 93499759 | 16 | p.S627F | 0.14-0.43 | Missense | Deleterious | Unmutated |
1343 | 93487716 | 10 | p.K375Kfs*5 | 0.26-0.56 | Insertion | — | Mutated |
1424 | 93510649 | 17 | p.R699W | 0.31-0.64 | Missense | Deleterious | Mutated |
1431 | 93510649 | 17 | p.R699W | 0.46-0.77 | Missense | Deleterious | Unmutated |
1535 | 93552489 | 35 | p.G1510R | 0.21-0.65 | Missense | Deleterious | Mutated |
MBL | |||||||
152 | 93444511 | 2 | p.L15Hfs*79 | 0.24-0.71 | Insertion | — | — |
190 | 93487649 | 10 | p.G353W | 0.09-0.48 | Missense | Neutral | — |
383 | 93524650 | 24 | p.T1011Nfs*6 | 0.19-0.44 | Insertion | — | — |
AF, allelic frequency (95% CI); CI, confidence interval.