Incidental Mutations

40 incidental mutations are currently displayed, and affect 40 genes.
4 are Possibly Damaging.
17 are Probably Damaging.
16 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 40 of 40] 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 437833 UTSW Abca15 0.075 R5596 G1 225 Y 7 120401749 M1503V A G missense Het possibly damaging 0.944 0.179 10/26/2016
2 437827 UTSW Abraxas1 0.251 R5596 G1 225 Y 5 100818537 V53D A T missense Het probably damaging 1.000 0.251 phenotype 10/26/2016
3 437810 UTSW Bub1b 1.000 R5596 G1 225 Y 2 118630982 S672P T C missense Het probably damaging 0.999 0.117 phenotype 10/26/2016
4 437825 UTSW C1qtnf7 0.000 R5596 G1 225 N 5 43515970 A T start gained Het probably benign phenotype 10/26/2016
5 437820 UTSW C87499 0.385 R5596 G1 225 Y 4 88630055 E38K C T missense Het probably damaging 1.000 0.647 10/26/2016
6 437831 UTSW Cacng7 0.000 R5596 G1 225 Y 7 3366904 I262F A T missense Het probably benign 0.213 0.060 phenotype 10/26/2016
7 437822 UTSW Capzb 1.000 R5596 G1 225 Y 4 139279427 T G intron Het probably benign 0.090 phenotype 10/26/2016
8 437826 UTSW Ccdc149 0.102 R5596 G1 225 Y 5 52404151 V229A A G missense Het probably damaging 0.961 0.097 10/26/2016
9 437824 UTSW Cfap69 0.000 R5596 G1 225 Y 5 5626020 L225P A G missense Het probably damaging 1.000 0.694 phenotype 10/26/2016
10 437829 UTSW Cftr 0.247 R5596 G1 225 Y 6 18268096 T685A A G missense Het probably benign 0.002 0.141 phenotype 10/26/2016
11 437837 UTSW Col12a1 0.681 R5596 G1 225 Y 9 79703759 T177M G A missense Het probably damaging 1.000 0.647 phenotype 10/26/2016
12 437840 UTSW Creb3l3 0.000 R5596 G1 225 Y 10 81085047 D383A T G missense Het probably benign 0.006 0.090 phenotype 10/26/2016
13 437821 UTSW Cyp2j8 0.090 R5596 G1 225 Y 4 96507341 I16F T A missense Het probably benign 0.001 0.090 10/26/2016
14 437845 UTSW Dnah5 0.737 R5596 G1 225 Y 15 28343608 A2385S G T missense Het probably damaging 1.000 0.469 phenotype 10/26/2016
15 437844 UTSW Enox1 0.000 R5596 G1 225 Y 14 77579053 I158V A G missense Het probably benign 0.423 0.104 phenotype 10/26/2016
16 486822 UTSW Erich3 0.000 R5596 G1 225 Y 3 154727396 T139S A T missense Het probably damaging 0.994 0.083 08/18/2017
17 437846 UTSW Fam186b 0.000 R5596 G1 225 Y 15 99271289 S926T A T missense Het possibly damaging 0.904 0.179 phenotype 10/26/2016
18 437809 UTSW Gjd2 0.194 R5596 G1 225 Y 2 114011484 V171F C A missense Het possibly damaging 0.926 0.094 phenotype 10/26/2016
19 457986 UTSW Gm13088 0.056 R5596 G1 225 N 4 143654455 T333S T A missense Het probably damaging 1.000 0.273 02/16/2017
20 437815 UTSW Helz2 0.000 R5596 G1 113 Y 2 181237289 A T intron Het probably benign 0.090 phenotype 10/26/2016
21 486823 UTSW Herc1 0.000 R5596 G1 134 N 9 66434063 T TTN critical splice acceptor site Het probably benign phenotype 08/18/2017
22 437838 UTSW Impg1 0.061 R5596 G1 225 Y 9 80345218 V483E A T missense Het probably benign 0.239 0.090 phenotype 10/26/2016
23 437843 UTSW Irx4 0.873 R5596 G1 225 Y 13 73267680 N196S A G missense Het probably damaging 1.000 0.958 phenotype 10/26/2016
24 486824 UTSW Kcnip1 0.098 R5596 G1 225 Y 11 33630597 D213G T C missense Het probably damaging 1.000 0.741 phenotype 08/18/2017
25 437830 UTSW Lmntd1 0.060 R5596 G1 225 Y 6 145413414 T191S T A missense Het probably benign 0.342 0.090 10/26/2016
26 437816 UTSW Med12l 0.293 R5596 G1 225 Y 3 59252350 N1273K T A missense Het probably benign 0.451 0.074 phenotype 10/26/2016
27 437819 UTSW Musk 1.000 R5596 G1 225 Y 4 58373036 C654R T C missense Het probably damaging 1.000 0.896 phenotype 10/26/2016
28 437832 UTSW Nlrp4d 0.000 R5596 G1 225 Y 7 10382024 S274T A T missense Het noncoding transcript 10/26/2016
29 437842 UTSW Omd 0.078 R5596 G1 225 Y 13 49592338 H408R A G missense Het probably benign 0.163 0.067 phenotype 10/26/2016
30 437839 UTSW Pbld2 0.000 R5596 G1 225 Y 10 63072012 A219V C T missense Het probably damaging 0.997 0.610 10/26/2016
31 437813 UTSW Ptpn1 0.898 R5596 G1 225 Y 2 167974763 I246T T C missense Het probably damaging 0.996 0.910 phenotype 10/26/2016
32 437835 UTSW Sap18b 0.936 R5596 G1 191 Y 8 95825370 A3S G T missense Het unknown 0.102 phenotype 10/26/2016
33 437811 UTSW Sptbn5 0.326 R5596 G1 166 Y 2 120046484 G A unclassified Het probably benign 0.069 10/26/2016
34 437812 UTSW Sstr4 0.179 R5596 G1 225 Y 2 148395732 V88F G T missense Het possibly damaging 0.655 0.179 phenotype 10/26/2016
35 437817 UTSW Tdpoz4 0.781 R5596 G1 225 Y 3 93797499 T368S A T missense Het probably benign 0.070 0.090 10/26/2016
36 437808 UTSW Tmcc2 0.128 R5596 G1 189 Y 1 132360483 N489D T C missense Het probably damaging 0.998 0.138 10/26/2016
37 437823 UTSW Tnfrsf9 0.091 R5596 G1 225 Y 4 150929874 V10A T C missense Het probably benign 0.015 0.090 phenotype 10/26/2016
38 457987 UTSW Tnxb 0.000 R5596 G1 225 N 17 34688804 V1274E T A missense Het probably damaging 1.000 phenotype 02/16/2017
39 437828 UTSW Ube3b 1.000 R5596 G1 225 Y 5 114406160 T A splice site Het probably null 0.976 phenotype 10/26/2016
40 437836 UTSW Vwa5a 0.000 R5596 G1 225 Y 9 38722578 I26F A T missense Het probably damaging 1.000 0.648 10/26/2016
[records 1 to 40 of 40]