Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
4 are Possibly Damaging.
12 are Probably Damaging.
5 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 91683 APN Abcb4 0.000 IGL01594 G1 5 8946071 A T unclassified 4984 bp Het probably null phenotype 12/09/2013
2 91690 APN Acss1 0.000 IGL01594 G1 2 150621530 V618E A T missense Het probably damaging 0.977 phenotype 12/09/2013
3 91673 APN Adgrg6 1.000 IGL01594 G1 10 14434340 N774D T C missense Het probably damaging 1.000 phenotype 12/09/2013
4 91678 APN Atp9a 0.000 IGL01594 G1 2 168691012 V134A A G missense Het probably damaging 0.998 12/09/2013
5 91686 APN Csmd3 0.000 IGL01594 G1 15 47629239 T3169S T A missense Het probably benign 0.008 12/09/2013
6 91677 APN D030068K23Rik 0.310 IGL01594 G1 8 109251377 Q52L T A missense Het unknown 12/09/2013
7 91680 APN Dnah5 0.779 IGL01594 G1 15 28311334 S1820P T C missense Het possibly damaging 0.870 phenotype 12/09/2013
8 91679 APN Fem1c 0.000 IGL01594 G1 18 46506276 S220A A C missense Het probably benign 0.001 phenotype 12/09/2013
9 91685 APN Gm10305 0.205 IGL01594 G1 4 99273177 D108N G A missense Het unknown 12/09/2013
10 91694 APN Gtdc1 0.088 IGL01594 G1 2 44591879 A G critical splice donor site 2 bp Het probably null 12/09/2013
11 91682 APN Il2ra 0.000 IGL01594 G1 2 11680396 V181A T C missense Het possibly damaging 0.845 phenotype 12/09/2013
12 91689 APN Lrrn1 0.406 IGL01594 G1 6 107567493 I84T T C missense Het probably damaging 0.986 phenotype 12/09/2013
13 91693 APN Map3k1 0.928 IGL01594 G1 13 111758189 T A critical splice acceptor site Het probably null phenotype 12/09/2013
14 91674 APN Mical1 0.186 IGL01594 G1 10 41480329 Y293D T G missense Het probably damaging 1.000 phenotype 12/09/2013
15 91672 APN Mpzl1 0.000 IGL01594 G1 1 165593592 D266G T C missense Het probably damaging 1.000 phenotype 12/09/2013
16 91692 APN Olfr544 0.094 IGL01594 G1 7 102485047 M24I C A missense Het probably benign 0.000 phenotype 12/09/2013
17 91676 APN Pabpc4l 0.000 IGL01594 G1 3 46447146 V21D A T missense Het probably damaging 1.000 12/09/2013
18 91688 APN Prdm10 1.000 IGL01594 G1 9 31346853 C525R T C missense Het probably damaging 0.999 phenotype 12/09/2013
19 91695 APN Ptprj 0.159 IGL01594 G1 2 90440795 C A splice site Het probably benign phenotype 12/09/2013
20 91691 APN Rgs3 0.174 IGL01594 G1 4 62619744 F4S T C missense Het probably damaging 0.989 phenotype 12/09/2013
21 91684 APN Ryr3 0.331 IGL01594 G1 2 112772728 T2457I G A missense Het probably damaging 1.000 phenotype 12/09/2013
22 91671 APN Scn3a 1.000 IGL01594 G1 2 65461431 I1657T A G missense Het probably damaging 1.000 phenotype 12/09/2013
23 91687 APN Sema6a 0.000 IGL01594 G1 18 47248817 S888P A G missense Het probably damaging 1.000 phenotype 12/09/2013
24 91681 APN Slc37a1 0.000 IGL01594 G1 17 31319148 Y148* T A nonsense Het probably null phenotype 12/09/2013
25 91675 APN Tex10 0.963 IGL01594 G1 4 48469906 N53S T C missense Het possibly damaging 0.466 phenotype 12/09/2013
26 91696 APN Tyr 0.178 IGL01594 G1 7 87483814 A T splice site Het probably benign phenotype 12/09/2013
27 91670 APN Vmn2r100 0.089 IGL01594 G1 17 19531233 S513G A G missense Het possibly damaging 0.524 12/09/2013
[records 1 to 27 of 27]