Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
2 are Possibly Damaging.
26 are Probably Damaging.
13 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 43 of 43] 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 406604 APN Adam5 0.057 IGL02982 8 24804431 (GRCm38) A384D G T missense Het probably benign 0.020 phenotype 2016-08-02
2 406590 APN Adamts19 0.000 IGL02982 18 59024518 (GRCm38) C961S T A missense Het probably damaging 1.000 phenotype 2016-08-02
3 406582 APN Agbl2 0.000 IGL02982 2 90805815 (GRCm38) C565Y G A missense Het probably damaging 0.996 phenotype 2016-08-02
4 406572 APN Aox3 0.000 IGL02982 1 58127687 (GRCm38) E190K G A missense Het probably benign 0.001 2016-08-02
5 406593 APN Arf2 0.000 IGL02982 11 103981776 (GRCm38) D74E T G missense Het probably damaging 0.974 2016-08-02
6 406568 APN Bptf 1.000 IGL02982 11 107076674 (GRCm38) D960A T G missense Het probably damaging 0.998 phenotype 2016-08-02
7 406608 APN Ccdc180 0.000 IGL02982 4 45903840 (GRCm38) G T splice site Het probably benign phenotype 2016-08-02
8 406577 APN Ces1a 0.000 IGL02982 8 93044975 (GRCm38) F65L A G missense Het probably damaging 1.000 2016-08-02
9 406607 APN Def8 0.185 IGL02982 8 123456539 (GRCm38) T C unclassified Het probably benign 2016-08-02
10 406576 APN Fat4 1.000 IGL02982 3 38890843 (GRCm38) L1295P T C missense Het probably damaging 1.000 phenotype 2016-08-02
11 406578 APN Filip1l 0.000 IGL02982 16 57572232 (GRCm38) H1061R A G missense Het probably damaging 1.000 2016-08-02
12 406592 APN Fut2 0.000 IGL02982 7 45650769 (GRCm38) G193E C T missense Het possibly damaging 0.939 phenotype 2016-08-02
13 406609 APN Gldc 1.000 IGL02982 19 30145145 (GRCm38) A G critical splice donor site 2 bp Het probably null phenotype 2016-08-02
14 406594 APN Gm597 0.070 IGL02982 1 28778054 (GRCm38) H299R T C missense Het probably damaging 1.000 2016-08-02
15 406605 APN Golgb1 0.900 IGL02982 16 36925810 (GRCm38) D2917A A C missense Het probably damaging 0.975 phenotype 2016-08-02
16 406598 APN Gpc5 0.000 IGL02982 14 115369988 (GRCm38) C334Y G A missense Het probably damaging 1.000 phenotype 2016-08-02
17 406589 APN Gpsm1 0.000 IGL02982 2 26324859 (GRCm38) L252Q T A missense Het probably damaging 1.000 phenotype 2016-08-02
18 406587 APN Iars 1.000 IGL02982 13 49709709 (GRCm38) R546C C T missense Het probably benign 0.004 phenotype 2016-08-02
19 406591 APN Kbtbd8 0.460 IGL02982 6 95126566 (GRCm38) V399L G T missense Het probably benign 0.006 2016-08-02
20 406581 APN Kcnd2 0.094 IGL02982 6 21217149 (GRCm38) D284V A T missense Het probably damaging 0.998 phenotype 2016-08-02
21 406574 APN Kcnj6 0.114 IGL02982 16 94832517 (GRCm38) K227R T C missense Het possibly damaging 0.891 phenotype 2016-08-02
22 406570 APN Lhx9 0.811 IGL02982 1 138838611 (GRCm38) H155Q A T missense Het probably damaging 1.000 phenotype 2016-08-02
23 406595 APN Mcm9 0.000 IGL02982 10 53625826 (GRCm38) V221A A G missense Het probably damaging 0.988 phenotype 2016-08-02
24 406569 APN Myo9a 0.000 IGL02982 9 59908208 (GRCm38) K2237* A T nonsense Het probably null phenotype 2016-08-02
25 406586 APN Ntf3 1.000 IGL02982 6 126102377 (GRCm38) D55E A T missense Het probably damaging 0.994 phenotype 2016-08-02
26 406602 APN Olfr1229 0.062 IGL02982 2 89283109 (GRCm38) T29K G T missense Het probably damaging 0.981 phenotype 2016-08-02
27 406567 APN Olfr61 0.072 IGL02982 7 140637952 (GRCm38) I84F A T missense Het probably benign 0.057 phenotype 2016-08-02
28 406597 APN Plek 0.243 IGL02982 11 16981826 (GRCm38) I342F T A missense Het probably damaging 0.998 phenotype 2016-08-02
29 406583 APN Polrmt 0.960 IGL02982 10 79738348 (GRCm38) Y853H A G missense Het probably damaging 1.000 phenotype 2016-08-02
30 406600 APN Psg29 0.053 IGL02982 7 17211707 (GRCm38) T401A A G missense Het probably damaging 0.981 2016-08-02
31 406603 APN Ptprb 1.000 IGL02982 10 116322628 (GRCm38) T822A A G missense Het probably benign 0.199 phenotype 2016-08-02
32 406588 APN Ptprq 0.252 IGL02982 10 107586684 (GRCm38) F1616V A C missense Het probably damaging 0.999 phenotype 2016-08-02
33 406599 APN Rpe65 0.123 IGL02982 3 159600361 (GRCm38) V19E T A missense Het probably damaging 0.993 phenotype 2016-08-02
34 406596 APN Scamp2 0.000 IGL02982 9 57581549 (GRCm38) A178T G A missense Het probably benign 0.000 phenotype 2016-08-02
35 406580 APN Spta1 0.911 IGL02982 1 174187288 (GRCm38) I445V A G missense Het probably benign 0.002 phenotype 2016-08-02
36 406573 APN Tas2r135 0.051 IGL02982 6 42406253 (GRCm38) E242G A G missense Het probably benign 0.000 2016-08-02
37 406601 APN Ttc22 0.054 IGL02982 4 106638586 (GRCm38) V379A T C missense Het probably damaging 0.966 phenotype 2016-08-02
38 406606 APN Unc5d 0.377 IGL02982 8 28652853 (GRCm38) G857E C T missense Het probably damaging 0.999 phenotype 2016-08-02
39 406579 APN Usp28 0.000 IGL02982 9 49018439 (GRCm38) I43V A G missense Het probably benign 0.003 phenotype 2016-08-02
40 406575 APN Vmn2r68 0.074 IGL02982 7 85234441 (GRCm38) M152K A T missense Het probably benign 0.120 2016-08-02
41 406584 APN Wrn 0.268 IGL02982 8 33343066 (GRCm38) G133R C T missense Het probably damaging 1.000 phenotype 2016-08-02
42 406571 APN Zfyve26 0.000 IGL02982 12 79263870 (GRCm38) T187M G A missense Het probably damaging 0.993 phenotype 2016-08-02
43 406585 APN Zic2 0.875 IGL02982 14 122478567 (GRCm38) E367G A G missense Het probably damaging 0.982 phenotype 2016-08-02
[records 1 to 43 of 43]