Incidental Mutations

48 incidental mutations are currently displayed, and affect 48 genes.
9 are Possibly Damaging.
21 are Probably Damaging.
14 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 48 of 48] 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 406999 APN 2310035C23Rik 0.453 IGL02992 1 105719464 L684M T A missense Het possibly damaging 0.888 08/02/2016
2 406994 APN Abca4 0.000 IGL02992 3 122128286 K1164E A G missense Het probably damaging 0.957 phenotype 08/02/2016
3 407011 APN Arhgap42 0.875 IGL02992 9 8998248 G A splice site Het probably benign phenotype 08/02/2016
4 406964 APN Arhgef12 0.830 IGL02992 9 42999077 D612G T C missense Het probably damaging 1.000 phenotype 08/02/2016
5 406980 APN Cpne3 0.303 IGL02992 4 19532486 D309G T C missense Het probably benign 0.000 phenotype 08/02/2016
6 407009 APN Daw1 0.261 IGL02992 1 83197213 T C splice site Het probably benign phenotype 08/02/2016
7 406998 APN Daxx 1.000 IGL02992 17 33911748 C246S T A missense Het probably damaging 1.000 phenotype 08/02/2016
8 406987 APN Dpp7 0.182 IGL02992 2 25354577 D264G T C missense Het possibly damaging 0.648 phenotype 08/02/2016
9 406989 APN Dync2h1 1.000 IGL02992 9 7137074 H1472L T A missense Het probably benign 0.010 phenotype 08/02/2016
10 407008 APN Fastkd2 0.431 IGL02992 1 63737924 T C splice site Het probably benign phenotype 08/02/2016
11 406983 APN Fcrls 0.097 IGL02992 3 87259466 R73S T G missense Het probably damaging 0.987 phenotype 08/02/2016
12 407002 APN Gatb 0.953 IGL02992 3 85618916 D367G A G missense Het probably damaging 0.999 08/02/2016
13 406988 APN Gm20547 IGL02992 17 34857119 E654V T A missense Het probably damaging 0.981 phenotype 08/02/2016
14 406986 APN Gm839 0.167 IGL02992 6 89212527 T A exon Het noncoding transcript 08/02/2016
15 406995 APN Gtf2ird2 0.172 IGL02992 5 134217614 M905L A T missense Het possibly damaging 0.785 08/02/2016
16 407000 APN Hoxb2 0.714 IGL02992 11 96353084 I174F A T missense Het probably damaging 1.000 phenotype 08/02/2016
17 406990 APN Hrh3 0.243 IGL02992 2 180100815 V308A A G missense Het probably benign 0.110 phenotype 08/02/2016
18 406968 APN Ints9 0.976 IGL02992 14 64980164 K47E A G missense Het probably benign 0.082 phenotype 08/02/2016
19 406970 APN Irak3 0.391 IGL02992 10 120182661 Y61N A T missense Het probably damaging 0.995 phenotype 08/02/2016
20 407001 APN Itpr1 0.612 IGL02992 6 108381315 E614G A G missense Het probably damaging 1.000 phenotype 08/02/2016
21 406996 APN Lgals3 IGL02992 14 47385525 I214L A T missense Het probably benign 0.065 phenotype 08/02/2016
22 406997 APN Msh4 0.542 IGL02992 3 153872325 T444K G T missense Het possibly damaging 0.792 phenotype 08/02/2016
23 406984 APN Myh7b 0.415 IGL02992 2 155621410 Q521K C A missense Het probably damaging 0.994 phenotype 08/02/2016
24 406979 APN Naip5 0.078 IGL02992 13 100223028 I567F T A missense Het probably damaging 1.000 phenotype 08/02/2016
25 407007 APN Nf1 1.000 IGL02992 11 79434933 A G splice site Het probably benign phenotype 08/02/2016
26 407010 APN Nlrc3 0.160 IGL02992 16 3954023 C T splice site Het probably benign phenotype 08/02/2016
27 406967 APN Nlrc5 0.000 IGL02992 8 94506573 E1353A A C missense Het possibly damaging 0.692 phenotype 08/02/2016
28 406993 APN Nr1h3 0.000 IGL02992 2 91190566 I260F T A missense Het probably damaging 0.999 phenotype 08/02/2016
29 406978 APN Pcnx 0.000 IGL02992 12 81964120 R1211Q G A missense Het probably damaging 1.000 phenotype 08/02/2016
30 406991 APN Pde10a 0.000 IGL02992 17 8949461 K605E A G missense Het probably damaging 0.971 phenotype 08/02/2016
31 406969 APN Pdzd2 0.243 IGL02992 15 12382622 E1215G T C missense Het possibly damaging 0.775 phenotype 08/02/2016
32 406982 APN Pex12 0.188 IGL02992 11 83297927 S81P A G missense Het probably damaging 1.000 phenotype 08/02/2016
33 406974 APN Pik3c2b 0.252 IGL02992 1 133066980 Y227* C A nonsense Het probably null phenotype 08/02/2016
34 406992 APN Ppef2 0.000 IGL02992 5 92235900 W450* C T nonsense Het probably null 0.480 phenotype 08/02/2016
35 406973 APN Prkg2 0.294 IGL02992 5 99024506 S117R T G missense Het probably benign 0.000 phenotype 08/02/2016
36 406965 APN Prl3d2 0.073 IGL02992 13 27127283 E179D A T missense Het probably benign 0.002 08/02/2016
37 407006 APN Rxfp2 0.000 IGL02992 5 150051556 V210A T C missense Het probably benign 0.015 0.062 phenotype 08/02/2016
38 406976 APN Scn10a 0.348 IGL02992 9 119609560 T1748A T C missense Het possibly damaging 0.897 phenotype 08/02/2016
39 406975 APN Sept10 0.181 IGL02992 10 59192178 N107S T C missense Het possibly damaging 0.870 phenotype 08/02/2016
40 407004 APN Smu1 0.955 IGL02992 4 40739550 N420I T A missense Het probably damaging 0.969 08/02/2016
41 407003 APN Sos1 1.000 IGL02992 17 80419016 F835L A G missense Het probably benign 0.012 phenotype 08/02/2016
42 406977 APN Spg11 0.477 IGL02992 2 122058398 D2164G T C missense Het probably damaging 0.998 phenotype 08/02/2016
43 406985 APN Svbp 0.101 IGL02992 4 119195930 E8G A G missense Het probably damaging 0.999 08/02/2016
44 406981 APN Tgm3 0.088 IGL02992 2 130041979 M519K T A missense Het probably damaging 1.000 phenotype 08/02/2016
45 407005 APN Tspan12 0.281 IGL02992 6 21799877 A G critical splice donor site 2 bp Het probably null phenotype 08/02/2016
46 406972 APN Vps52 1.000 IGL02992 17 33958350 V122A T C missense Het probably damaging 0.966 phenotype 08/02/2016
47 406966 APN Wipf1 0.238 IGL02992 2 73434083 Y458C T C missense Het probably damaging 1.000 phenotype 08/02/2016
48 406971 APN Zfp369 0.181 IGL02992 13 65294451 D286E T A missense Het possibly damaging 0.505 08/02/2016
[records 1 to 48 of 48]