Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
6 are Possibly Damaging.
17 are Probably Damaging.
15 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44] 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 284680 APN Abcc9 0.117 IGL02210 6 142687371 (GRCm38) F215S A G missense Het probably damaging 1.000 phenotype 2015-04-16
2 284672 APN Acvr2a 0.000 IGL02210 2 48898526 (GRCm38) H422L A T missense Het probably damaging 0.992 phenotype 2015-04-16
3 284678 APN Adcy6 0.000 IGL02210 15 98594971 (GRCm38) Y908C T C missense Het possibly damaging 0.634 phenotype 2015-04-16
4 284661 APN Alyref 0.951 IGL02210 11 120597673 (GRCm38) S110A A C missense Het possibly damaging 0.783 2015-04-16
5 284667 APN Ankrd1 0.000 IGL02210 19 36118314 (GRCm38) D86G T C missense Het probably damaging 0.998 phenotype 2015-04-16
6 284660 APN Anpep 0.000 IGL02210 7 79826904 (GRCm38) Y29F T A missense Het probably benign 0.002 phenotype 2015-04-16
7 284691 APN Appl1 0.188 IGL02210 14 26925952 (GRCm38) T C splice site Het probably benign phenotype 2015-04-16
8 284666 APN Arrdc5 0.000 IGL02210 17 56300026 (GRCm38) D73G T C missense Het probably damaging 0.996 2015-04-16
9 284659 APN Atp12a 0.000 IGL02210 14 56371744 (GRCm38) Y142* T A nonsense Het probably null phenotype 2015-04-16
10 284674 APN Clec4a3 0.000 IGL02210 6 122954108 (GRCm38) I52N T A missense Het probably damaging 0.984 2015-04-16
11 284669 APN Cmya5 0.204 IGL02210 13 93092734 (GRCm38) P1949S G A missense Het probably benign 0.135 2015-04-16
12 284682 APN Crybb2 0.317 IGL02210 5 113058387 (GRCm38) Q194L T A missense Het probably damaging 0.995 phenotype 2015-04-16
13 284668 APN Dmxl2 1.000 IGL02210 9 54404049 (GRCm38) L1796R A C missense Het probably damaging 1.000 phenotype 2015-04-16
14 284657 APN Ecm1 0.169 IGL02210 3 95735977 (GRCm38) F337S A G missense Het probably damaging 0.966 phenotype 2015-04-16
15 284671 APN F5 1.000 IGL02210 1 164190141 (GRCm38) S596P T C missense Het probably benign 0.001 phenotype 2015-04-16
16 284675 APN Fat4 1.000 IGL02210 3 38891853 (GRCm38) T1632A A G missense Het probably benign 0.010 phenotype 2015-04-16
17 284683 APN Gm5070 0.234 IGL02210 3 95410625 (GRCm38) T G unclassified Het noncoding transcript 2015-04-16
18 284676 APN Hps5 0.095 IGL02210 7 46786570 (GRCm38) Y184C T C missense Het probably benign 0.026 phenotype 2015-04-16
19 284690 APN Letmd1 0.164 IGL02210 15 100469247 (GRCm38) T C critical splice donor site 2 bp Het probably null phenotype 2015-04-16
20 284658 APN Lipo5 0.068 IGL02210 19 33467877 (GRCm38) N97K A T missense Het unknown 2015-04-16
21 284670 APN Mis18bp1 1.000 IGL02210 12 65136831 (GRCm38) Y922* A T nonsense Het probably null 2015-04-16
22 284656 APN Mob3c 0.198 IGL02210 4 115833755 (GRCm38) H181N C A missense Het probably damaging 0.999 phenotype 2015-04-16
23 284649 APN Muc4 0.099 IGL02210 16 32752254 (GRCm38) T711S A T missense Het probably benign 0.002 0.090 phenotype 2015-04-16
24 284662 APN Nav3 0.000 IGL02210 10 109766990 (GRCm38) T1233A T C missense Het probably benign 0.000 phenotype 2015-04-16
25 284653 APN Olfr1120 0.253 IGL02210 2 87358003 (GRCm38) D186E T A missense Het probably damaging 1.000 phenotype 2015-04-16
26 284654 APN Olfr361 0.143 IGL02210 2 37085619 (GRCm38) T43N G T missense Het possibly damaging 0.539 phenotype 2015-04-16
27 284685 APN Pcnt 1.000 IGL02210 10 76389219 (GRCm38) E1817G T C missense Het possibly damaging 0.951 phenotype 2015-04-16
28 284652 APN Pdzd3 0.000 IGL02210 9 44248317 (GRCm38) T461P T G missense Het probably benign 0.000 phenotype 2015-04-16
29 284681 APN Phc3 0.000 IGL02210 3 30936709 (GRCm38) V420A A G missense Het probably damaging 0.989 2015-04-16
30 284673 APN Plekhn1 0.102 IGL02210 4 156223649 (GRCm38) C316S A T missense Het probably damaging 0.999 2015-04-16
31 284692 APN Ppp1cb 1.000 IGL02210 5 32483474 (GRCm38) T A splice site Het probably benign phenotype 2015-04-16
32 284651 APN Slc29a4 0.000 IGL02210 5 142718779 (GRCm38) Y359H T C missense Het probably damaging 0.999 phenotype 2015-04-16
33 284686 APN Sspo 0.000 IGL02210 6 48500492 (GRCm38) I4982T T C missense Het probably damaging 1.000 2015-04-16
34 284650 APN Sstr4 0.261 IGL02210 2 148396309 (GRCm38) L280Q T A missense Het probably damaging 0.998 phenotype 2015-04-16
35 284689 APN Stap1 0.150 IGL02210 5 86078061 (GRCm38) G A critical splice donor site 1 bp Het probably null phenotype 2015-04-16
36 284663 APN Szt2 0.518 IGL02210 4 118389823 (GRCm38) V865A A G missense Het possibly damaging 0.954 phenotype 2015-04-16
37 284679 APN Tmem246 0.090 IGL02210 4 49586686 (GRCm38) Y161H A G missense Het probably benign 0.000 2015-04-16
38 284665 APN Tnr 0.000 IGL02210 1 159852101 (GRCm38) V215D T A missense Het probably benign 0.441 phenotype 2015-04-16
39 284664 APN Trpm1 0.000 IGL02210 7 64210865 (GRCm38) L288P T C missense Het probably damaging 1.000 phenotype 2015-04-16
40 284688 APN Ttll5 0.458 IGL02210 12 85912545 (GRCm38) T A intron Het probably benign phenotype 2015-04-16
41 284687 APN Usp8 1.000 IGL02210 2 126718056 (GRCm38) T C intron Het probably benign phenotype 2015-04-16
42 284684 APN Uxs1 1.000 IGL02210 1 43750286 (GRCm38) Y403C T C missense Het possibly damaging 0.947 phenotype 2015-04-16
43 284677 APN Wnk2 0.315 IGL02210 13 49090869 (GRCm38) E497G T C missense Het probably damaging 0.981 phenotype 2015-04-16
44 284655 APN Xdh 0.326 IGL02210 17 73943895 (GRCm38) K21E T C missense Het probably benign 0.003 phenotype 2015-04-16
[records 1 to 44 of 44]