Incidental Mutations

38 incidental mutations are currently displayed, and affect 38 genes.
5 are Possibly Damaging.
14 are Probably Damaging.
14 are Probably Benign.
5 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 28597 APN Alox12b 1.000 IGL00959 G1 11 69166243 H430L A T missense Het probably damaging 1.000 phenotype 04/17/2013
2 26718 APN Aox4 0.000 IGL00959 G1 1 58239174 V443F G T missense Het probably damaging 0.998 phenotype 04/17/2013
3 26719 APN Bmpr2 1.000 IGL00959 G1 1 59815315 I108F A T missense Het possibly damaging 0.878 phenotype 04/17/2013
4 26720 APN Cflar 1.000 IGL00959 G1 1 58729162 G A critical splice donor site 1 bp Het probably null phenotype 04/17/2013
5 27679 APN Chchd3 1.000 IGL00959 G1 6 32968253 V106A A G missense Het probably benign 0.157 phenotype 04/17/2013
6 278123 APN Chl1 0.456 IGL00959 G1 6 103709250 G T splice site 5 bp Het probably null phenotype 04/16/2015
7 28383 APN Clvs2 0.102 IGL00959 G1 10 33528463 M252I C T missense Het probably benign 0.026 phenotype 04/17/2013
8 26717 APN Cntnap5a 0.000 IGL00959 G1 1 116184327 L449Q T A missense Het probably benign 0.001 phenotype 04/17/2013
9 28382 APN Col6a2 0.000 IGL00959 G1 10 76614534 I188F T A missense Het probably damaging 0.962 phenotype 04/17/2013
10 29532 APN Cyp2c55 0.080 IGL00959 G1 19 39038143 D398G A G missense Het probably benign 0.003 0.090 phenotype 04/17/2013
11 26721 APN Dennd1b 0.000 IGL00959 G1 1 139143888 T C splice site Het probably benign phenotype 04/17/2013
12 28225 APN Dopey1 0.238 IGL00959 G1 9 86487431 Y106N T A missense Het probably damaging 1.000 04/17/2013
13 28226 APN Dpy19l1 0.205 IGL00959 G1 9 24423197 A T splice site Het probably null 04/17/2013
14 28972 APN Extl3 1.000 IGL00959 G1 14 65076912 V274I C T missense Het probably benign 0.006 phenotype 04/17/2013
15 27484 APN Fras1 0.000 IGL00959 G1 5 96781281 R3848H G A missense Het probably damaging 0.964 phenotype 04/17/2013
16 28599 APN Gm11437 0.114 IGL00959 G1 11 84148622 A C intron Het probably benign 04/17/2013
17 26968 APN Gss 1.000 IGL00959 G1 2 155581951 D2V T A missense Het probably damaging 0.999 phenotype 04/17/2013
18 278122 APN Hnrnpm 1.000 IGL00959 G1 17 33649902 R517L C A missense Het probably damaging 0.988 phenotype 04/16/2015
19 28381 APN Ilvbl 0.124 IGL00959 G1 10 78583905 D548N G A missense Het probably damaging 1.000 phenotype 04/17/2013
20 28598 APN Jmjd6 1.000 IGL00959 G1 11 116842376 D115E A T missense Het possibly damaging 0.683 phenotype 04/17/2013
21 28770 APN Kidins220 1.000 IGL00959 G1 12 25051133 S1110R T A missense Het possibly damaging 0.740 phenotype 04/17/2013
22 27483 APN Kmt2c 1.000 IGL00959 G1 5 25276229 I4784F T A missense Het probably damaging 0.999 phenotype 04/17/2013
23 28973 APN Mrpl52 IGL00959 G1 14 54427037 V11A T C missense Het possibly damaging 0.634 phenotype 04/17/2013
24 26969 APN Myo3b 0.000 IGL00959 G1 2 70314292 Y1036C A G missense Het probably damaging 0.999 phenotype 04/17/2013
25 28384 APN Olfr769 0.076 IGL00959 G1 10 129112024 M134L T A missense Het probably benign 0.014 phenotype 04/17/2013
26 27884 APN Omp 0.082 IGL00959 G1 7 98145150 D90G T C missense Het probably damaging 0.998 phenotype 04/17/2013
27 29086 APN Osmr 0.067 IGL00959 G1 15 6824605 I541V T C missense Het probably benign 0.119 phenotype 04/17/2013
28 29533 APN Ppp1r32 0.000 IGL00959 G1 19 10477523 A T critical splice donor site 2 bp Het probably null 04/17/2013
29 29320 APN Ppp2r1a 1.000 IGL00959 G1 17 20961578 A T unclassified Het probably benign phenotype 04/17/2013
30 27485 APN Ptpn13 0.281 IGL00959 G1 5 103517571 T A critical splice donor site 2 bp Het probably null phenotype 04/17/2013
31 28769 APN Rock2 0.860 IGL00959 G1 12 16978055 N1429K C A missense Het probably benign 0.113 phenotype 04/17/2013
32 28224 APN Slc25a20 1.000 IGL00959 G1 9 108681999 M188R T G missense Het possibly damaging 0.864 phenotype 04/17/2013
33 27885 APN Slc28a1 0.094 IGL00959 G1 7 81169068 T C splice site Het probably benign 04/17/2013
34 27883 APN Sult2a6 0.061 IGL00959 G1 7 14254709 Y42C T C missense Het probably damaging 1.000 phenotype 04/17/2013
35 26716 APN Tgfb2 1.000 IGL00959 G1 1 186704587 V63A A G missense Het probably benign 0.394 phenotype 04/17/2013
36 27482 APN Ugt2b38 0.063 IGL00959 G1 5 87411823 N403K A T missense Het probably damaging 1.000 04/17/2013
37 27882 APN Vmn2r29 IGL00959 G1 7 7241856 W340R A G missense Het probably benign 0.003 04/17/2013
38 28974 APN Wnt5a 1.000 IGL00959 G1 14 28522909 T351M C T missense Het probably damaging 0.995 phenotype 04/17/2013
[records 1 to 38 of 38]