Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
4 are Possibly Damaging.
15 are Probably Damaging.
17 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 43 of 43] 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 420732 APN 9930021J03Rik 0.097 IGL03382 19 29717276 G1606R C T missense Het probably damaging 0.996 08/02/2016
2 420738 APN Aff1 0.394 IGL03382 5 103841060 D831G A G missense Het possibly damaging 0.860 phenotype 08/02/2016
3 420751 APN Amer2 0.142 IGL03382 14 60379882 K509E A G missense Het possibly damaging 0.766 08/02/2016
4 420739 APN Ankrd6 0.000 IGL03382 4 32808771 K449E T C missense Het probably damaging 0.998 phenotype 08/02/2016
5 420735 APN Atp8b2 0.179 IGL03382 3 89948521 P459L G A missense Het probably benign 0.004 phenotype 08/02/2016
6 420723 APN Atr 1.000 IGL03382 9 95920822 R1846* C T nonsense Het probably null phenotype 08/02/2016
7 420756 APN Ccdc159 0.000 IGL03382 9 21931696 C A splice site Het probably null 08/02/2016
8 420729 APN Ccna1 0.351 IGL03382 3 55047277 Y338D A C missense Het probably damaging 1.000 phenotype 08/02/2016
9 420725 APN Cpq 0.699 IGL03382 15 33212943 E36V A T missense Het probably damaging 0.957 phenotype 08/02/2016
10 420750 APN Cyp2c23 0.000 IGL03382 19 44014932 I268T A G missense Het probably damaging 0.985 phenotype 08/02/2016
11 420744 APN Dctn2 1.000 IGL03382 10 127278188 Q332H G T missense Het probably damaging 0.991 phenotype 08/02/2016
12 420737 APN Dnah17 0.000 IGL03382 11 118081943 I2055F T A missense Het probably damaging 1.000 phenotype 08/02/2016
13 420733 APN Dnmt3b 1.000 IGL03382 2 153686359 H764R A G missense Het probably damaging 0.999 phenotype 08/02/2016
14 420716 APN Gphn 1.000 IGL03382 12 78481313 I135K T A missense Het probably damaging 1.000 phenotype 08/02/2016
15 420730 APN Hnrnpul1 0.577 IGL03382 7 25750984 M1T A G start codon destroyed Het probably null 0.533 phenotype 08/02/2016
16 420748 APN Htra4 0.000 IGL03382 8 25029698 D406G T C missense Het probably benign 0.168 phenotype 08/02/2016
17 420755 APN Klk10 0.061 IGL03382 7 43784459 G T splice site Het probably benign phenotype 08/02/2016
18 420718 APN Lilrb4a 0.195 IGL03382 10 51491520 W53R T A missense Het probably benign 0.101 phenotype 08/02/2016
19 420747 APN Magel2 1.000 IGL03382 7 62378713 V455A T C missense Het probably benign 0.001 phenotype 08/02/2016
20 420728 APN Mrgprb5 0.060 IGL03382 7 48168694 T98A T C missense Het probably benign 0.006 08/02/2016
21 420714 APN Mrps35 0.952 IGL03382 6 147049875 C76* T A nonsense Het probably null phenotype 08/02/2016
22 420727 APN Myh7b 0.000 IGL03382 2 155623479 R701C C T missense Het probably damaging 1.000 phenotype 08/02/2016
23 420754 APN Nbeal1 0.000 IGL03382 1 60261586 G A critical splice donor site 1 bp Het probably null 0.949 08/02/2016
24 420726 APN Neb 0.881 IGL03382 2 52325708 M196L T A missense Het probably benign 0.001 phenotype 08/02/2016
25 420719 APN Nmd3 0.961 IGL03382 3 69735088 K207R A G missense Het probably damaging 0.994 phenotype 08/02/2016
26 420742 APN Plxna4 0.648 IGL03382 6 32202194 R962Q C T missense Het probably benign 0.233 phenotype 08/02/2016
27 420741 APN Pom121 1.000 IGL03382 5 135392407 K230E T C missense Het unknown 08/02/2016
28 420720 APN Psme4 0.000 IGL03382 11 30807788 D307G A G missense Het possibly damaging 0.941 phenotype 08/02/2016
29 420746 APN Rnf41 0.000 IGL03382 10 128438280 M267R T G missense Het possibly damaging 0.909 phenotype 08/02/2016
30 420734 APN Sis 0.000 IGL03382 3 72928719 N846D T C missense Het probably benign 0.002 phenotype 08/02/2016
31 420722 APN Slc22a19 0.058 IGL03382 19 7681862 I463L T A missense Het probably benign 0.006 phenotype 08/02/2016
32 420753 APN Slc25a39 0.907 IGL03382 11 102406204 A T critical splice donor site 2 bp Het probably null phenotype 08/02/2016
33 420745 APN Slc35b2 0.110 IGL03382 17 45566645 R233C C T missense Het probably damaging 0.980 phenotype 08/02/2016
34 420740 APN Slc4a4 1.000 IGL03382 5 89228836 L983P T C missense Het probably damaging 1.000 phenotype 08/02/2016
35 420724 APN Sp110 0.351 IGL03382 1 85577329 F434C A C missense Het probably benign 0.000 0.090 08/02/2016
36 420736 APN Tbc1d10a 0.000 IGL03382 11 4209984 Y123C A G missense Het probably damaging 1.000 phenotype 08/02/2016
37 420721 APN Thbs4 0.000 IGL03382 13 92769548 I395S A C missense Het probably benign 0.365 phenotype 08/02/2016
38 420743 APN Triml2 0.061 IGL03382 8 43193739 T422A A G missense Het probably benign 0.001 phenotype 08/02/2016
39 420752 APN Ubn2 0.870 IGL03382 6 38440447 T C unclassified Het probably benign 08/02/2016
40 420715 APN Vmn1r15 0.136 IGL03382 6 57258570 M141K T A missense Het probably benign 0.043 08/02/2016
41 420717 APN Vmn2r80 0.125 IGL03382 10 79169528 E333G A G missense Het probably damaging 0.999 08/02/2016
42 420731 APN Zfp169 0.070 IGL03382 13 48491163 T C unclassified Het probably benign phenotype 08/02/2016
43 420749 APN Zfp942 0.069 IGL03382 17 21929102 P182L G A missense Het probably benign 0.038 08/02/2016
[records 1 to 43 of 43]