Incidental Mutations

38 incidental mutations are currently displayed, and affect 37 genes.
8 are Possibly Damaging.
11 are Probably Damaging.
17 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38] 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 362874 APN 1810055G02Rik 0.062 IGL02883 19 3716972 (GRCm38) S186R C A missense Het possibly damaging 0.827 2015-12-18
2 362897 APN Acap2 0.149 IGL02883 16 31096345 (GRCm38) A G unclassified Het probably benign 2015-12-18
3 362868 APN Cacna1h 0.000 IGL02883 17 25380532 (GRCm38) R1726S G T missense Het probably damaging 1.000 phenotype 2015-12-18
4 362890 APN Cdca2 0.083 IGL02883 14 67707497 (GRCm38) S133G T C missense Het probably damaging 0.999 phenotype 2015-12-18
5 362887 APN Cep295nl 0.000 IGL02883 11 118333909 (GRCm38) S36R A T missense Het probably benign 0.008 2015-12-18
6 362885 APN Crispld1 0.079 IGL02883 1 17746789 (GRCm38) N190S A G missense Het possibly damaging 0.870 2015-12-18
7 362870 APN Crtam 0.062 IGL02883 9 40994501 (GRCm38) V44A A G missense Het probably benign 0.000 phenotype 2015-12-18
8 362867 APN Crtc1 0.456 IGL02883 8 70406125 (GRCm38) G112S C T missense Het probably benign 0.276 phenotype 2015-12-18
9 362894 APN Cyp17a1 0.200 IGL02883 19 46669351 (GRCm38) N254S T C missense Het probably benign 0.001 phenotype 2015-12-18
10 362875 APN Dmrta1 0.000 IGL02883 4 89688774 (GRCm38) S156P T C missense Het probably benign 0.000 phenotype 2015-12-18
11 362877 APN Eno2 0.219 IGL02883 6 124766209 (GRCm38) V188G A C missense Het probably damaging 0.999 phenotype 2015-12-18
12 362878 APN Fam20a 0.000 IGL02883 11 109675127 (GRCm38) I427N A T missense Het probably damaging 0.990 phenotype 2015-12-18
13 362888 APN Fat2 0.000 IGL02883 11 55256618 (GRCm38) K3933E T C missense Het probably benign 0.161 phenotype 2015-12-18
14 362862 APN Gm15448 0.048 IGL02883 7 3822180 (GRCm38) S488P A G missense Het possibly damaging 0.955 2015-12-18
15 362861 APN Igkv8-30 0.118 IGL02883 6 70117617 (GRCm38) M1V T C start codon destroyed Het probably null 0.845 2015-12-18
16 362896 APN Ist1 0.866 IGL02883 8 109683668 (GRCm38) G A splice site Het probably benign phenotype 2015-12-18
17 362892 APN Kank4 0.071 IGL02883 4 98773453 (GRCm38) E765G T C missense Het possibly damaging 0.865 2015-12-18
18 362889 APN Kat14 1.000 IGL02883 2 144393529 (GRCm38) L92S T C missense Het probably damaging 1.000 phenotype 2015-12-18
19 362879 APN Kcnu1 0.000 IGL02883 8 25849827 (GRCm38) V58I G A missense Het probably benign 0.000 phenotype 2015-12-18
20 362886 APN Lrba 0.000 IGL02883 3 86445413 (GRCm38) I1956N T A missense Het probably damaging 0.993 phenotype 2015-12-18
21 362882 APN Lrba 0.000 IGL02883 3 86354206 (GRCm38) V1489E T A missense Het probably damaging 0.999 phenotype 2015-12-18
22 362883 APN Mdn1 1.000 IGL02883 4 32763199 (GRCm38) V5100I G A missense Het probably benign 0.051 2015-12-18
23 362884 APN Mkrn2os 0.070 IGL02883 6 115586709 (GRCm38) G122* C A nonsense Het probably null 2015-12-18
24 362873 APN Nme3 0.173 IGL02883 17 24896906 (GRCm38) Y78H T C missense Het probably benign 0.316 phenotype 2015-12-18
25 362864 APN Pkd1l2 0.000 IGL02883 8 117065745 (GRCm38) T436I G A missense Het probably benign 0.070 0.072 phenotype 2015-12-18
26 362869 APN Ppp2r5c 0.000 IGL02883 12 110522563 (GRCm38) V56G T G missense Het possibly damaging 0.480 phenotype 2015-12-18
27 362865 APN Pramef25 0.060 IGL02883 4 143949848 (GRCm38) T229A T C missense Het possibly damaging 0.642 2015-12-18
28 362872 APN Prdm10 1.000 IGL02883 9 31327348 (GRCm38) V179M G A missense Het probably damaging 0.989 phenotype 2015-12-18
29 362891 APN Rab11fip2 0.162 IGL02883 19 59906998 (GRCm38) V344A A G missense Het probably damaging 1.000 2015-12-18
30 362866 APN Selp 0.104 IGL02883 1 164130102 (GRCm38) A267T G A missense Het probably benign 0.004 phenotype 2015-12-18
31 362876 APN Sf3a1 1.000 IGL02883 11 4179192 (GRCm38) W718R T A missense Het probably damaging 0.998 phenotype 2015-12-18
32 362863 APN Taar9 0.080 IGL02883 10 24109480 (GRCm38) N19D T C missense Het probably benign 0.084 phenotype 2015-12-18
33 362880 APN Tas2r113 0.060 IGL02883 6 132893419 (GRCm38) S137A T G missense Het probably damaging 0.999 2015-12-18
34 362871 APN Traf4 0.914 IGL02883 11 78161621 (GRCm38) I66N A T missense Het possibly damaging 0.716 phenotype 2015-12-18
35 362893 APN Ucp3 0.060 IGL02883 7 100480642 (GRCm38) T164S A T missense Het probably benign 0.003 phenotype 2015-12-18
36 362881 APN Uggt1 0.466 IGL02883 1 36177615 (GRCm38) N96K A T missense Het probably benign 0.030 phenotype 2015-12-18
37 362895 APN Uqcc1 0.926 IGL02883 2 155911829 (GRCm38) Q42L T A missense Het possibly damaging 0.934 phenotype 2015-12-18
38 362860 APN Vmn1r128 IGL02883 7 21349515 (GRCm38) K48R A G missense Het probably benign 0.001 2015-12-18
[records 1 to 38 of 38]