Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
9 are Possibly Damaging.
12 are Probably Damaging.
12 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 34 of 34] 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 89513 APN 4932438A13Rik 1.000 IGL01524 G1 3 36942382 D1081G A G missense Het possibly damaging 0.901 phenotype 12/03/2013
2 89515 APN Aadat 0.000 IGL01524 G1 8 60516072 D117V A T missense Het probably damaging 0.973 phenotype 12/03/2013
3 89514 APN Abca14 0.000 IGL01524 G1 7 120253421 Y870H T C missense Het possibly damaging 0.572 12/03/2013
4 89507 APN Ankrd36 0.055 IGL01524 G1 11 5635092 I301T T C missense Het probably benign 0.000 12/03/2013
5 89492 APN Atp10b 0.093 IGL01524 G1 11 43259845 S1457T T A missense Het probably benign 0.177 12/03/2013
6 89522 APN Ccdc175 0.056 IGL01524 G1 12 72131142 G A splice site Het probably benign 12/03/2013
7 89498 APN Ccdc93 0.181 IGL01524 G1 1 121461899 K224E A G missense Het probably benign 0.049 12/03/2013
8 89497 APN Cep131 0.950 IGL01524 G1 11 120065960 A886T C T missense Het probably damaging 1.000 phenotype 12/03/2013
9 89503 APN Clip1 0.000 IGL01524 G1 5 123579379 H1282Q A C missense Het probably damaging 1.000 phenotype 12/03/2013
10 89494 APN Ctcfl 0.406 IGL01524 G1 2 173117384 D183A T G missense Het probably benign 0.075 phenotype 12/03/2013
11 89505 APN Cyp17a1 0.241 IGL01524 G1 19 46671056 V112I C T missense Het probably benign 0.004 phenotype 12/03/2013
12 89519 APN D3Ertd254e 0.097 IGL01524 G1 3 36164580 Y251H T C missense Het possibly damaging 0.861 12/03/2013
13 89512 APN Fhod3 1.000 IGL01524 G1 18 25130602 I1521T T C missense Het probably damaging 0.992 phenotype 12/03/2013
14 89504 APN Gipc2 0.172 IGL01524 G1 3 152137577 I141T A G missense Het probably damaging 1.000 12/03/2013
15 89506 APN Glo1 IGL01524 G1 17 30596419 R141G T C missense Het possibly damaging 0.750 phenotype 12/03/2013
16 89491 APN Ipmk 1.000 IGL01524 G1 10 71372801 A140E C A missense Het probably damaging 1.000 phenotype 12/03/2013
17 89517 APN Kynu 0.000 IGL01524 G1 2 43671382 D310G A G missense Het possibly damaging 0.906 phenotype 12/03/2013
18 89508 APN Myo1f 0.152 IGL01524 G1 17 33579883 I174N T A missense Het probably damaging 1.000 phenotype 12/03/2013
19 89496 APN Nat10 1.000 IGL01524 G1 2 103757757 N8Y T A missense Het probably damaging 1.000 phenotype 12/03/2013
20 89521 APN Nhlrc2 1.000 IGL01524 G1 19 56576155 I304V A G missense Het probably benign 0.393 12/03/2013
21 89499 APN Pdk4 0.000 IGL01524 G1 6 5491979 H31R T C missense Het probably damaging 1.000 phenotype 12/03/2013
22 89516 APN Sema6d 0.000 IGL01524 G1 2 124664075 V644A T C missense Het possibly damaging 0.857 phenotype 12/03/2013
23 89495 APN Slc30a4 0.000 IGL01524 G1 2 122702388 K11N T A missense Het possibly damaging 0.871 phenotype 12/03/2013
24 89520 APN Slc6a3 0.000 IGL01524 G1 13 73538549 S12P T C missense Het probably benign 0.008 phenotype 12/03/2013
25 89510 APN Spats2 0.481 IGL01524 G1 15 99212246 A508V C T missense Het probably benign 0.003 12/03/2013
26 89509 APN Tinag 0.142 IGL01524 G1 9 77045538 Y55H A G missense Het probably damaging 1.000 phenotype 12/03/2013
27 89500 APN Topbp1 1.000 IGL01524 G1 9 103311645 I172T T C missense Het possibly damaging 0.915 phenotype 12/03/2013
28 89511 APN Trim17 0.000 IGL01524 G1 11 58970597 T279A A G missense Het probably damaging 1.000 phenotype 12/03/2013
29 89490 APN Vmn1r216 0.190 IGL01524 G1 13 23099349 N67K C A missense Het probably benign 0.194 12/03/2013
30 89493 APN Washc4 0.953 IGL01524 G1 10 83576132 L709P T C missense Het probably benign 0.373 phenotype 12/03/2013
31 89523 APN Xdh 0.421 IGL01524 G1 17 73923137 T C critical splice acceptor site Het probably null phenotype 12/03/2013
32 89501 APN Zfhx4 0.724 IGL01524 G1 3 5243976 P754L C T missense Het probably damaging 1.000 12/03/2013
33 89518 APN Zfp623 0.382 IGL01524 G1 15 75947679 S161R C A missense Het probably benign 0.000 12/03/2013
34 89502 APN Zmat3 0.167 IGL01524 G1 3 32341678 R227C G A missense Het possibly damaging 0.822 phenotype 12/03/2013
[records 1 to 34 of 34]