Incidental Mutations

46 incidental mutations are currently displayed, and affect 46 genes.
7 are Possibly Damaging.
18 are Probably Damaging.
19 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46] 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 294788 APN 1110038F14Rik IGL02472 15 76950378 N158S A G missense Het probably damaging 0.976 04/16/2015
2 294789 APN Ankrd17 1.000 IGL02472 5 90264151 L1285V A C missense Het probably damaging 1.000 phenotype 04/16/2015
3 294784 APN Atp8b2 0.249 IGL02472 3 89954239 T267I G A missense Het probably damaging 1.000 phenotype 04/16/2015
4 294781 APN Becn1 1.000 IGL02472 11 101291398 G115D C T missense Het probably benign 0.032 phenotype 04/16/2015
5 294790 APN Cd3eap 1.000 IGL02472 7 19359105 D50G T C missense Het probably damaging 0.998 04/16/2015
6 294759 APN Cdc45 1.000 IGL02472 16 18798729 M200I C T missense Het probably benign 0.059 0.115 phenotype 04/16/2015
7 294793 APN Chd6 0.806 IGL02472 2 160984452 A C splice site Het probably benign phenotype 04/16/2015
8 294792 APN Col22a1 0.000 IGL02472 15 71827753 A G splice site Het probably benign phenotype 04/16/2015
9 294787 APN Csgalnact1 0.070 IGL02472 8 68401492 G219V C A missense Het probably damaging 1.000 phenotype 04/16/2015
10 294761 APN Dnm2 1.000 IGL02472 9 21485708 I494V A G missense Het possibly damaging 0.554 phenotype 04/16/2015
11 294786 APN Dock2 0.000 IGL02472 11 34249801 E1416D T A missense Het probably benign 0.001 phenotype 04/16/2015
12 294778 APN Eif2ak1 0.139 IGL02472 5 143884883 H339R A G missense Het probably benign 0.001 phenotype 04/16/2015
13 294772 APN Espnl 0.000 IGL02472 1 91340534 P294L C T missense Het probably benign 0.016 04/16/2015
14 294760 APN Ftmt 0.000 IGL02472 18 52331840 I76N T A missense Het possibly damaging 0.922 phenotype 04/16/2015
15 294795 APN Gorasp2 0.120 IGL02472 2 70676459 T G splice site Het probably benign phenotype 04/16/2015
16 294776 APN Hadhb 0.169 IGL02472 5 30184063 M468K T A missense Het possibly damaging 0.684 phenotype 04/16/2015
17 294799 APN Hfm1 0.131 IGL02472 5 106873928 A G splice site Het probably benign phenotype 04/16/2015
18 294797 APN Inpp5j 0.324 IGL02472 11 3495338 T C unclassified Het probably benign phenotype 04/16/2015
19 294767 APN Ipo7 0.962 IGL02472 7 110040853 F288I T A missense Het probably damaging 1.000 phenotype 04/16/2015
20 294770 APN Kcnv1 0.000 IGL02472 15 45109123 K455* T A nonsense Het probably null phenotype 04/16/2015
21 294800 APN Kdm5a 1.000 IGL02472 6 120406730 A G splice site Het probably benign phenotype 04/16/2015
22 294766 APN Kmt2d 1.000 IGL02472 15 98850077 S3122F G A missense Het probably benign 0.226 phenotype 04/16/2015
23 294785 APN Kndc1 0.000 IGL02472 7 139910901 I440V A G missense Het probably benign 0.008 phenotype 04/16/2015
24 294783 APN Mib2 0.000 IGL02472 4 155656746 I545F T A missense Het probably damaging 0.996 phenotype 04/16/2015
25 294773 APN Nav2 0.626 IGL02472 7 49546041 P1055L C T missense Het probably damaging 1.000 phenotype 04/16/2015
26 294765 APN Olfr111 0.665 IGL02472 17 37530749 F257L C A missense Het probably damaging 0.999 phenotype 04/16/2015
27 294757 APN Olfr1257 0.068 IGL02472 2 89881411 I195N T A missense Het probably benign 0.444 phenotype 04/16/2015
28 294764 APN Plch1 0.120 IGL02472 3 63701849 L65Q A T missense Het probably damaging 1.000 phenotype 04/16/2015
29 294755 APN Ppp3ca 0.000 IGL02472 3 136921862 I396V A G missense Het possibly damaging 0.571 phenotype 04/16/2015
30 294768 APN Ryr1 1.000 IGL02472 7 29040844 N3917K A T missense Het probably damaging 0.999 phenotype 04/16/2015
31 294769 APN Scn7a 0.112 IGL02472 2 66752314 T80A T C missense Het probably damaging 0.999 phenotype 04/16/2015
32 294762 APN Sema3f 0.000 IGL02472 9 107687736 E307K C T missense Het probably damaging 1.000 phenotype 04/16/2015
33 294791 APN Serpinb9b 0.000 IGL02472 13 33039970 A T utr 3 prime Het probably benign 04/16/2015
34 294782 APN Siglec15 0.000 IGL02472 18 78043617 K342N T A missense Het possibly damaging 0.719 phenotype 04/16/2015
35 294774 APN Slc2a12 0.000 IGL02472 10 22665155 F303S T C missense Het probably damaging 1.000 phenotype 04/16/2015
36 294780 APN Slc9c1 0.585 IGL02472 16 45580142 V705A T C missense Het probably benign 0.099 phenotype 04/16/2015
37 294794 APN Tenm4 1.000 IGL02472 7 96774176 T C unclassified Het probably benign phenotype 04/16/2015
38 294796 APN Tm6sf1 0.070 IGL02472 7 81875824 A T splice site Het probably benign 04/16/2015
39 294779 APN Tmem245 0.748 IGL02472 4 56899119 Y269C T C missense Het probably damaging 1.000 04/16/2015
40 294771 APN Txndc2 0.148 IGL02472 17 65637976 I402T A G missense Het possibly damaging 0.861 phenotype 04/16/2015
41 294798 APN Ube4b 1.000 IGL02472 4 149387079 A G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
42 294775 APN Usp28 0.000 IGL02472 9 49037769 Y863N T A missense Het possibly damaging 0.955 phenotype 04/16/2015
43 294756 APN Vmn2r69 0.088 IGL02472 7 85409752 I534V T C missense Het probably benign 0.011 04/16/2015
44 294758 APN Wdr89 0.000 IGL02472 12 75632969 D170E A T missense Het probably damaging 0.999 phenotype 04/16/2015
45 294777 APN Zfp280d 0.365 IGL02472 9 72301711 N74K C A missense Het probably damaging 0.997 04/16/2015
46 294763 APN Zfp518a 0.896 IGL02472 19 40914617 G997R G A missense Het probably damaging 1.000 phenotype 04/16/2015
[records 1 to 46 of 46]