Incidental Mutations

47 incidental mutations are currently displayed, and affect 47 genes.
7 are Possibly Damaging.
15 are Probably Damaging.
20 are Probably Benign.
4 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 47 of 47] 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 290898 APN 1300017J02Rik 0.213 IGL02370 9 103263074 V482A A G missense Het probably benign 0.267 04/16/2015
2 290916 APN 4732471J01Rik IGL02370 7 25384888 T C unclassified Het probably benign phenotype 04/16/2015
3 290901 APN Abra 0.291 IGL02370 15 41869244 D142G T C missense Het probably damaging 1.000 phenotype 04/16/2015
4 290887 APN Aldh9a1 0.000 IGL02370 1 167356532 N199D A G missense Het probably damaging 1.000 phenotype 04/16/2015
5 290911 APN Baz2b 0.269 IGL02370 2 59923589 I1130N A T missense Het possibly damaging 0.770 phenotype 04/16/2015
6 290891 APN Cacna1s 1.000 IGL02370 1 136085347 I312V A G missense Het probably damaging 0.999 phenotype 04/16/2015
7 290910 APN Chrd 1.000 IGL02370 16 20735791 M367V A G missense Het possibly damaging 0.524 phenotype 04/16/2015
8 290883 APN Clec12a 0.049 IGL02370 6 129354576 A160V C T missense Het possibly damaging 0.577 phenotype 04/16/2015
9 290915 APN Cnnm1 0.161 IGL02370 19 43471950 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
10 290880 APN Cntnap3 0.059 IGL02370 13 64751751 M976K A T missense Het probably benign 0.000 phenotype 04/16/2015
11 290914 APN Cyp27b1 0.000 IGL02370 10 127050674 T C splice site Het probably benign phenotype 04/16/2015
12 290879 APN Ddx54 1.000 IGL02370 5 120619787 L226Q T A missense Het probably damaging 1.000 phenotype 04/16/2015
13 290889 APN Dnah7a 0.119 IGL02370 1 53635397 V407A A G missense Het probably benign 0.003 04/16/2015
14 290886 APN Elp4 0.965 IGL02370 2 105794592 S201P A G missense Het probably damaging 1.000 phenotype 04/16/2015
15 290899 APN Exoc3 0.968 IGL02370 13 74192761 V308D A T missense Het probably benign 0.017 phenotype 04/16/2015
16 290896 APN Exosc3 0.959 IGL02370 4 45319671 I117T A G missense Het probably damaging 0.999 phenotype 04/16/2015
17 290912 APN Gbx2 1.000 IGL02370 1 89929149 A T splice site Het probably benign phenotype 04/16/2015
18 290876 APN Gm4858 0.896 IGL02370 3 93074047 D124G A G missense Het possibly damaging 0.611 04/16/2015
19 290909 APN Hnf1b 1.000 IGL02370 11 83882733 T253P A C missense Het possibly damaging 0.939 phenotype 04/16/2015
20 290890 APN Itih5 0.065 IGL02370 2 10186975 Y107F A T missense Het probably benign 0.052 phenotype 04/16/2015
21 290906 APN Kcnb2 0.000 IGL02370 1 15710935 N677S A G missense Het probably benign 0.000 phenotype 04/16/2015
22 290918 APN Knstrn 0.000 IGL02370 2 118823788 T A critical splice donor site 2 bp Het probably null phenotype 04/16/2015
23 290892 APN Lin9 1.000 IGL02370 1 180688018 C451F G T missense Het probably damaging 0.997 phenotype 04/16/2015
24 290900 APN Mast1 0.000 IGL02370 8 84912254 V1482G A C missense Het probably benign 0.000 04/16/2015
25 290904 APN Mroh4 0.000 IGL02370 15 74625541 F144L A G missense Het probably benign 0.001 04/16/2015
26 290882 APN Myrf 0.899 IGL02370 19 10214140 N945D T C missense Het probably benign 0.000 phenotype 04/16/2015
27 290875 APN Nfrkb 0.678 IGL02370 9 31389012 G33D G A missense Het probably benign 0.079 04/16/2015
28 290874 APN Olfr1036 0.422 IGL02370 2 86074788 T16K C A missense Het probably damaging 0.978 phenotype 04/16/2015
29 290895 APN P2ry13 0.000 IGL02370 3 59209465 I297M T C missense Het probably damaging 1.000 phenotype 04/16/2015
30 290897 APN Pcdhb21 0.062 IGL02370 18 37514592 T A unclassified Het probably null phenotype 04/16/2015
31 290894 APN Pitpnm3 0.056 IGL02370 11 72051858 Y868H A G missense Het probably benign 0.040 phenotype 04/16/2015
32 290907 APN Pou2f3 0.000 IGL02370 9 43137348 R266W G A missense Het probably damaging 0.998 phenotype 04/16/2015
33 290878 APN Rcn3 1.000 IGL02370 7 45083333 S304G T C missense Het probably benign 0.000 04/16/2015
34 290913 APN Rinl 0.000 IGL02370 7 28794972 A G splice site Het probably null 04/16/2015
35 290917 APN Sema5a 1.000 IGL02370 15 32682299 T C splice site Het probably benign phenotype 04/16/2015
36 290903 APN Sipa1l2 0.348 IGL02370 8 125480269 L565P A G missense Het probably damaging 1.000 phenotype 04/16/2015
37 290881 APN Slc5a9 0.101 IGL02370 4 111877629 I656T A G missense Het probably benign 0.008 04/16/2015
38 290884 APN Sptan1 1.000 IGL02370 2 30030740 K2404R A G missense Het probably damaging 0.987 phenotype 04/16/2015
39 290905 APN Tarsl2 0.162 IGL02370 7 65661165 P314Q C A missense Het probably benign 0.174 04/16/2015
40 290902 APN Tbc1d14 1.000 IGL02370 5 36495218 V627I C T missense Het possibly damaging 0.681 phenotype 04/16/2015
41 290877 APN Tfcp2 0.000 IGL02370 15 100512304 V394D A T missense Het probably damaging 1.000 phenotype 04/16/2015
42 290885 APN Trerf1 0.474 IGL02370 17 47314461 C T exon Het noncoding transcript phenotype 04/16/2015
43 290873 APN Ucp2 0.143 IGL02370 7 100498384 N190S A G missense Het probably damaging 0.958 phenotype 04/16/2015
44 290872 APN Vmn2r124 0.089 IGL02370 17 18064191 Q498R A G missense Het probably benign 0.135 04/16/2015
45 290908 APN Yeats2 0.962 IGL02370 16 20150471 I4N T A missense Het probably damaging 0.990 phenotype 04/16/2015
46 290888 APN Zfp574 0.956 IGL02370 7 25079589 I12S T G missense Het possibly damaging 0.948 04/16/2015
47 290893 APN Zscan29 0.127 IGL02370 2 121163833 E522V T A missense Het probably benign 0.005 04/16/2015
[records 1 to 47 of 47]