Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
7 are Possibly Damaging.
9 are Probably Damaging.
20 are Probably Benign.
7 are Probably Null.
1 create premature stop codons.
3 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 406881 APN Alox12b 1.000 IGL02990 11 69163206 (GRCm38) V205F G T missense Het probably benign 0.166 phenotype 2016-08-02
2 406911 APN Ampd3 0.000 IGL02990 7 110807963 (GRCm38) T C splice site Het probably benign phenotype 2016-08-02
3 406873 APN Arhgef18 1.000 IGL02990 8 3444904 (GRCm38) V388I G A missense Het probably benign 0.019 phenotype 2016-08-02
4 406892 APN Atp6v1c2 0.346 IGL02990 12 17294740 (GRCm38) V169I C T missense Het probably damaging 1.000 phenotype 2016-08-02
5 406894 APN Ccdc88b 0.000 IGL02990 19 6847409 (GRCm38) L1328I G T missense Het probably damaging 1.000 phenotype 2016-08-02
6 406903 APN Ces1d 0.000 IGL02990 8 93169718 (GRCm38) C A splice site 3 bp Het probably null phenotype 2016-08-02
7 406909 APN Cluh 0.233 IGL02990 11 74667765 (GRCm38) G A splice site 5 bp Het probably null phenotype 2016-08-02
8 406886 APN Cpsf7 0.000 IGL02990 19 10531795 (GRCm38) N23K C A missense Het probably benign 0.000 phenotype 2016-08-02
9 406890 APN Cyp4x1 0.075 IGL02990 4 115121749 (GRCm38) F191L A T missense Het probably benign 0.020 phenotype 2016-08-02
10 406888 APN Dcn 0.000 IGL02990 10 97509973 (GRCm38) T216A A G missense Het probably benign 0.003 phenotype 2016-08-02
11 406896 APN Dirc2 0.901 IGL02990 16 35735491 (GRCm38) V200F C A missense Het possibly damaging 0.683 phenotype 2016-08-02
12 406907 APN Drosha 0.964 IGL02990 15 12827267 (GRCm38) C T unclassified Het probably benign phenotype 2016-08-02
13 406895 APN Foxn4 1.000 IGL02990 5 114272989 (GRCm38) S24P A G missense Het probably damaging 0.980 phenotype 2016-08-02
14 406914 APN Gm11733 IGL02990 11 117486983 (GRCm38) A T critical splice acceptor site Het probably null 2016-08-02
15 406878 APN Hapln1 1.000 IGL02990 13 89601606 (GRCm38) Y90S A C missense Het probably benign 0.032 phenotype 2016-08-02
16 406913 APN Igf2r 0.918 IGL02990 17 12710746 (GRCm38) C A splice site Het probably benign phenotype 2016-08-02
17 406904 APN Jade2 0.000 IGL02990 11 51831247 (GRCm38) A G splice site Het probably benign 2016-08-02
18 406891 APN Kcnh7 0.111 IGL02990 2 62705986 (GRCm38) L1084H A T missense Het probably benign 0.114 phenotype 2016-08-02
19 406901 APN Kif1a 0.867 IGL02990 1 93039263 (GRCm38) D1155G T C missense Het probably damaging 1.000 phenotype 2016-08-02
20 406902 APN Llgl2 0.668 IGL02990 11 115854333 (GRCm38) M958V A G missense Het probably benign 0.008 phenotype 2016-08-02
21 406883 APN Lrp2 1.000 IGL02990 2 69441396 (GRCm38) V4064A A G missense Het possibly damaging 0.565 phenotype 2016-08-02
22 406912 APN Mau2 1.000 IGL02990 8 70022255 (GRCm38) A G splice site Het probably benign phenotype 2016-08-02
23 406910 APN Mllt10 0.713 IGL02990 2 18123711 (GRCm38) T C splice site Het probably benign phenotype 2016-08-02
24 406875 APN Myo15 0.000 IGL02990 11 60479440 (GRCm38) T1009A A G missense Het probably benign 0.023 phenotype 2016-08-02
25 406906 APN Myo6 0.000 IGL02990 9 80276403 (GRCm38) T C critical splice donor site 2 bp Het probably null phenotype 2016-08-02
26 406889 APN Neil2 0.000 IGL02990 14 63191809 (GRCm38) H12N G T missense Het possibly damaging 0.713 phenotype 2016-08-02
27 406898 APN Nrde2 1.000 IGL02990 12 100142096 (GRCm38) E412G T C missense Het probably damaging 1.000 2016-08-02
28 406876 APN Olfr114 0.065 IGL02990 17 37589668 (GRCm38) M228I C T missense Het probably benign 0.002 phenotype 2016-08-02
29 406900 APN Olfr1220 0.053 IGL02990 2 89097129 (GRCm38) Y266C T C missense Het possibly damaging 0.936 phenotype 2016-08-02
30 406905 APN Patl2 0.095 IGL02990 2 122124497 (GRCm38) T G critical splice acceptor site Het probably null 2016-08-02
31 406887 APN Pkhd1 0.094 IGL02990 1 20522963 (GRCm38) H1642R T C missense Het possibly damaging 0.521 phenotype 2016-08-02
32 406897 APN Ppp6r1 0.136 IGL02990 7 4643023 (GRCm38) I199T A G missense Het possibly damaging 0.830 phenotype 2016-08-02
33 406893 APN Prom2 0.000 IGL02990 2 127528814 (GRCm38) T817S T A missense Het probably benign 0.100 phenotype 2016-08-02
34 406908 APN Slc9b1 0.131 IGL02990 3 135394983 (GRCm38) A G splice site 3 bp Het probably null phenotype 2016-08-02
35 406877 APN Sv2c 0.066 IGL02990 13 96088378 (GRCm38) I141K A T missense Het probably damaging 1.000 phenotype 2016-08-02
36 406882 APN Tas2r139 0.000 IGL02990 6 42141104 (GRCm38) I57F A T missense Het probably damaging 0.999 phenotype 2016-08-02
37 406884 APN Tep1 0.000 IGL02990 14 50868246 (GRCm38) S106P A G missense Het possibly damaging 0.856 phenotype 2016-08-02
38 406885 APN Tnni3k 0.261 IGL02990 3 154957758 (GRCm38) D319G T C missense Het probably benign 0.009 phenotype 2016-08-02
39 406899 APN Tom1l2 0.200 IGL02990 11 60230236 (GRCm38) D461N C T missense Het probably damaging 0.997 phenotype 2016-08-02
40 406874 APN Ugt1a10 0.098 IGL02990 1 88055879 (GRCm38) L133S T C missense Het probably damaging 1.000 2016-08-02
41 406880 APN Usf2 0.831 IGL02990 7 30955307 (GRCm38) Q161P T G missense Het probably benign 0.000 phenotype 2016-08-02
42 406879 APN Vmn1r15 0.117 IGL02990 6 57258608 (GRCm38) T154A A G missense Het probably benign 0.141 2016-08-02
43 406872 APN Vmn2r95 0.085 IGL02990 17 18452036 (GRCm38) Y678* C A nonsense Het probably null 2016-08-02
[records 1 to 43 of 43]