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 (GRCm38) D1081G A G missense Het possibly damaging 0.901 phenotype 2013-12-03
2 89515 APN Aadat 0.000 IGL01524 G1 8 60516072 (GRCm38) D117V A T missense Het probably damaging 0.973 phenotype 2013-12-03
3 89514 APN Abca14 0.000 IGL01524 G1 7 120253421 (GRCm38) Y870H T C missense Het possibly damaging 0.572 2013-12-03
4 89507 APN Ankrd36 0.052 IGL01524 G1 11 5635092 (GRCm38) I301T T C missense Het probably benign 0.000 2013-12-03
5 89492 APN Atp10b 0.083 IGL01524 G1 11 43259845 (GRCm38) S1457T T A missense Het probably benign 0.177 2013-12-03
6 89522 APN Ccdc175 0.056 IGL01524 G1 12 72131142 (GRCm38) G A splice site Het probably benign 2013-12-03
7 89498 APN Ccdc93 0.137 IGL01524 G1 1 121461899 (GRCm38) K224E A G missense Het probably benign 0.049 2013-12-03
8 89497 APN Cep131 0.951 IGL01524 G1 11 120065960 (GRCm38) A886T C T missense Het probably damaging 1.000 phenotype 2013-12-03
9 89503 APN Clip1 0.000 IGL01524 G1 5 123579379 (GRCm38) H1282Q A C missense Het probably damaging 1.000 phenotype 2013-12-03
10 89494 APN Ctcfl 0.441 IGL01524 G1 2 173117384 (GRCm38) D183A T G missense Het probably benign 0.075 phenotype 2013-12-03
11 89505 APN Cyp17a1 0.200 IGL01524 G1 19 46671056 (GRCm38) V112I C T missense Het probably benign 0.004 phenotype 2013-12-03
12 89519 APN D3Ertd254e 0.106 IGL01524 G1 3 36164580 (GRCm38) Y251H T C missense Het possibly damaging 0.861 2013-12-03
13 89512 APN Fhod3 1.000 IGL01524 G1 18 25130602 (GRCm38) I1521T T C missense Het probably damaging 0.992 phenotype 2013-12-03
14 89504 APN Gipc2 0.116 IGL01524 G1 3 152137577 (GRCm38) I141T A G missense Het probably damaging 1.000 2013-12-03
15 89506 APN Glo1 IGL01524 G1 17 30596419 (GRCm38) R141G T C missense Het possibly damaging 0.750 phenotype 2013-12-03
16 89491 APN Ipmk 1.000 IGL01524 G1 10 71372801 (GRCm38) A140E C A missense Het probably damaging 1.000 phenotype 2013-12-03
17 89517 APN Kynu 0.000 IGL01524 G1 2 43671382 (GRCm38) D310G A G missense Het possibly damaging 0.906 phenotype 2013-12-03
18 89508 APN Myo1f 0.252 IGL01524 G1 17 33579883 (GRCm38) I174N T A missense Het probably damaging 1.000 phenotype 2013-12-03
19 89496 APN Nat10 1.000 IGL01524 G1 2 103757757 (GRCm38) N8Y T A missense Het probably damaging 1.000 phenotype 2013-12-03
20 89521 APN Nhlrc2 1.000 IGL01524 G1 19 56576155 (GRCm38) I304V A G missense Het probably benign 0.393 2013-12-03
21 89499 APN Pdk4 0.000 IGL01524 G1 6 5491979 (GRCm38) H31R T C missense Het probably damaging 1.000 phenotype 2013-12-03
22 89516 APN Sema6d 0.000 IGL01524 G1 2 124664075 (GRCm38) V644A T C missense Het possibly damaging 0.857 phenotype 2013-12-03
23 89495 APN Slc30a4 0.000 IGL01524 G1 2 122702388 (GRCm38) K11N T A missense Het possibly damaging 0.871 phenotype 2013-12-03
24 89520 APN Slc6a3 0.000 IGL01524 G1 13 73538549 (GRCm38) S12P T C missense Het probably benign 0.008 phenotype 2013-12-03
25 89510 APN Spats2 0.409 IGL01524 G1 15 99212246 (GRCm38) A508V C T missense Het probably benign 0.003 2013-12-03
26 89509 APN Tinag 0.084 IGL01524 G1 9 77045538 (GRCm38) Y55H A G missense Het probably damaging 1.000 phenotype 2013-12-03
27 89500 APN Topbp1 1.000 IGL01524 G1 9 103311645 (GRCm38) I172T T C missense Het possibly damaging 0.915 phenotype 2013-12-03
28 89511 APN Trim17 0.000 IGL01524 G1 11 58970597 (GRCm38) T279A A G missense Het probably damaging 1.000 phenotype 2013-12-03
29 89490 APN Vmn1r216 0.312 IGL01524 G1 13 23099349 (GRCm38) N67K C A missense Het probably benign 0.194 2013-12-03
30 89493 APN Washc4 0.955 IGL01524 G1 10 83576132 (GRCm38) L709P T C missense Het probably benign 0.373 phenotype 2013-12-03
31 89523 APN Xdh 0.326 IGL01524 G1 17 73923137 (GRCm38) T C critical splice acceptor site Het probably null phenotype 2013-12-03
32 89501 APN Zfhx4 0.622 IGL01524 G1 3 5243976 (GRCm38) P754L C T missense Het probably damaging 1.000 2013-12-03
33 89518 APN Zfp623 0.446 IGL01524 G1 15 75947679 (GRCm38) S161R C A missense Het probably benign 0.000 2013-12-03
34 89502 APN Zmat3 0.102 IGL01524 G1 3 32341678 (GRCm38) R227C G A missense Het possibly damaging 0.822 phenotype 2013-12-03
[records 1 to 34 of 34]