Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
4 are Possibly Damaging.
12 are Probably Damaging.
13 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30] 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 364885 APN Aadacl4 0.057 IGL02949 4 144617920 V89I G A missense Het probably damaging 0.996 12/18/2015
2 364872 APN Abhd5 0.000 IGL02949 9 122377915 F89L T C missense Het possibly damaging 0.509 phenotype 12/18/2015
3 364879 APN Akr1c13 0.068 IGL02949 13 4198594 V266E T A missense Het probably damaging 0.994 12/18/2015
4 364896 APN B4galt2 0.401 IGL02949 4 117881405 A72T C T missense Het probably benign 0.048 phenotype 12/18/2015
5 364895 APN Ccdc141 0.000 IGL02949 2 77027594 Y1081C T C missense Het probably damaging 1.000 phenotype 12/18/2015
6 364888 APN Coq8b 1.000 IGL02949 7 27256613 V405A T C missense Het possibly damaging 0.696 phenotype 12/18/2015
7 364886 APN Ddah2 0.154 IGL02949 17 35061800 K251E A G missense Het probably damaging 0.969 phenotype 12/18/2015
8 364894 APN Dnah5 0.828 IGL02949 15 28272185 V1045A T C missense Het probably benign 0.320 phenotype 12/18/2015
9 364875 APN Dpy19l1 0.147 IGL02949 9 24421180 M662K A T missense Het probably benign 0.436 12/18/2015
10 364870 APN Dpys 0.095 IGL02949 15 39826883 V358A A G missense Het probably damaging 0.972 phenotype 12/18/2015
11 364876 APN H2-D1 0.097 IGL02949 17 35264088 N198S A G missense Het probably benign 0.017 phenotype 12/18/2015
12 364871 APN Hnrnpa1 0.904 IGL02949 15 103242111 V163A T C missense Het probably damaging 1.000 phenotype 12/18/2015
13 364883 APN Hr 0.000 IGL02949 14 70559785 R543C C T missense Het possibly damaging 0.873 phenotype 12/18/2015
14 364878 APN Lct 0.000 IGL02949 1 128313132 V245M C T missense Het probably benign 0.259 phenotype 12/18/2015
15 364890 APN Lpl 1.000 IGL02949 8 68892748 V135M G A missense Het probably damaging 1.000 phenotype 12/18/2015
16 364880 APN Mblac1 0.322 IGL02949 5 138194857 C154S T A missense Het probably benign 0.002 12/18/2015
17 364881 APN Mmp9 0.000 IGL02949 2 164951119 F396S T C missense Het probably damaging 1.000 phenotype 12/18/2015
18 364887 APN Mroh1 0.087 IGL02949 15 76408968 H314L A T missense Het probably damaging 0.969 12/18/2015
19 364897 APN Msantd4 0.284 IGL02949 9 4385196 L307Q T A missense Het probably damaging 0.999 12/18/2015
20 364874 APN Nol8 1.000 IGL02949 13 49662402 D662G A G missense Het probably benign 0.012 phenotype 12/18/2015
21 364884 APN Nynrin 0.000 IGL02949 14 55872380 S1648N G A missense Het probably damaging 0.994 12/18/2015
22 364869 APN Olfr243 0.083 IGL02949 7 103717220 I209V A G missense Het probably benign 0.001 phenotype 12/18/2015
23 364898 APN Plcb2 0.000 IGL02949 2 118719109 C T splice site 5 bp Het probably null phenotype 12/18/2015
24 364873 APN Scyl2 0.386 IGL02949 10 89660301 N229I T A missense Het possibly damaging 0.819 phenotype 12/18/2015
25 364892 APN Spryd3 0.000 IGL02949 15 102118109 E376K C T missense Het probably benign 0.031 12/18/2015
26 364882 APN Srr 0.359 IGL02949 11 74908737 E304A T G missense Het probably benign 0.002 phenotype 12/18/2015
27 364891 APN Srsf1 1.000 IGL02949 11 88049526 A G intron Het probably benign phenotype 12/18/2015
28 364877 APN Txnrd2 1.000 IGL02949 16 18477706 S473A T G missense Het probably benign 0.002 phenotype 12/18/2015
29 364893 APN Wdr18 0.964 IGL02949 10 79965055 C151S T A missense Het probably benign 0.001 phenotype 12/18/2015
30 364889 APN Zfp282 0.085 IGL02949 6 47897914 T351I C T missense Het probably damaging 0.998 12/18/2015
[records 1 to 30 of 30]