Incidental Mutations

45 incidental mutations are currently displayed, and affect 45 genes.
10 are Possibly Damaging.
13 are Probably Damaging.
16 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 45 of 45] 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 410283 APN Agtpbp1 0.692 IGL03130 13 59474589 E941G T C missense Het possibly damaging 0.727 phenotype 08/02/2016
2 410292 APN AI314180 0.340 IGL03130 4 58800288 C1806S A T missense Het probably benign 0.000 08/02/2016
3 410269 APN Akap11 0.000 IGL03130 14 78510368 Y1526* A T nonsense Het probably null phenotype 08/02/2016
4 410284 APN Brd1 1.000 IGL03130 15 88688374 I1165V T C missense Het probably benign 0.000 phenotype 08/02/2016
5 410304 APN Btbd11 0.128 IGL03130 10 85388483 G T splice site 5 bp Het probably null 08/02/2016
6 410266 APN Cdan1 1.000 IGL03130 2 120727912 D473G T C missense Het possibly damaging 0.936 phenotype 08/02/2016
7 410278 APN Clstn3 0.000 IGL03130 6 124459263 L176F G A missense Het probably damaging 0.975 phenotype 08/02/2016
8 410261 APN Ctif 0.126 IGL03130 18 75521618 N279S T C missense Het probably benign 0.000 phenotype 08/02/2016
9 410263 APN Dpy19l3 0.132 IGL03130 7 35752672 S16P A G missense Het probably benign 0.001 08/02/2016
10 410297 APN Fam151b 0.000 IGL03130 13 92450193 Y244C T C missense Het probably benign 0.014 08/02/2016
11 410270 APN Gbf1 1.000 IGL03130 19 46267348 M750T T C missense Het possibly damaging 0.817 phenotype 08/02/2016
12 410298 APN Gm11564 0.073 IGL03130 11 99815053 T184S T A missense Het unknown 08/02/2016
13 410287 APN Gnptab 0.936 IGL03130 10 88436371 K958E A G missense Het possibly damaging 0.946 phenotype 08/02/2016
14 410279 APN Hibch 0.457 IGL03130 1 52885151 S162P T C missense Het possibly damaging 0.885 phenotype 08/02/2016
15 410288 APN Itpr1 0.813 IGL03130 6 108523401 S2651P T C missense Het probably benign 0.001 phenotype 08/02/2016
16 410267 APN Lyrm1 0.330 IGL03130 7 119914180 D56G A G missense Het probably damaging 1.000 phenotype 08/02/2016
17 410291 APN Manba 0.104 IGL03130 3 135551159 Y528H T C missense Het probably damaging 1.000 phenotype 08/02/2016
18 410268 APN Npas2 0.000 IGL03130 1 39313028 E186D A C missense Het probably damaging 1.000 phenotype 08/02/2016
19 410285 APN Olfr1314 0.060 IGL03130 2 112091821 D293E A T missense Het probably benign 0.000 phenotype 08/02/2016
20 410265 APN Olfr371 0.061 IGL03130 8 85230629 I45F A T missense Het possibly damaging 0.931 phenotype 08/02/2016
21 410293 APN Olfr867 0.085 IGL03130 9 20055372 L30F C A missense Het probably benign 0.336 phenotype 08/02/2016
22 410294 APN Oraov1 0.891 IGL03130 7 144916460 E42G A G missense Het probably damaging 0.999 08/02/2016
23 410264 APN Pcdhb6 0.100 IGL03130 18 37335587 Y520* T A nonsense Het probably null 08/02/2016
24 410289 APN Plekhm1 0.000 IGL03130 11 103377381 R588H C T missense Het probably benign 0.166 phenotype 08/02/2016
25 410276 APN Psg23 0.000 IGL03130 7 18610416 H371Q A T missense Het probably benign 0.255 phenotype 08/02/2016
26 410305 APN Ptpn12 1.000 IGL03130 5 21002612 T C unclassified Het probably benign phenotype 08/02/2016
27 410275 APN Rela 1.000 IGL03130 19 5639881 C120R T C missense Het probably damaging 1.000 phenotype 08/02/2016
28 410274 APN Rps6kc1 0.000 IGL03130 1 190799811 I665F T A missense Het probably damaging 0.999 08/02/2016
29 410295 APN Spg21 0.160 IGL03130 9 65473708 Q99R A G missense Het probably benign 0.009 phenotype 08/02/2016
30 410303 APN St14 1.000 IGL03130 9 31097071 A G critical splice donor site 2 bp Het probably null phenotype 08/02/2016
31 410296 APN Sult1c2 0.056 IGL03130 17 53830071 N274K A T missense Het probably benign 0.381 phenotype 08/02/2016
32 410271 APN Syk 1.000 IGL03130 13 52622732 V256A T C missense Het probably benign 0.124 phenotype 08/02/2016
33 410290 APN Tcte1 0.000 IGL03130 17 45533296 D66G A G missense Het probably damaging 1.000 08/02/2016
34 410277 APN Tgm4 0.057 IGL03130 9 123056515 T374M C T missense Het probably damaging 0.997 phenotype 08/02/2016
35 410280 APN Tns4 0.302 IGL03130 11 99068269 H668R T C missense Het probably damaging 1.000 08/02/2016
36 410282 APN Tsn 0.416 IGL03130 1 118305269 A102T C T missense Het possibly damaging 0.618 phenotype 08/02/2016
37 410273 APN Uvssa 0.077 IGL03130 5 33391845 S350T T A missense Het possibly damaging 0.566 phenotype 08/02/2016
38 410262 APN Vmn1r3 0.244 IGL03130 4 3185214 Y31F T A missense Het possibly damaging 0.887 08/02/2016
39 410302 APN Vmn2r114 0.092 IGL03130 17 23296996 A T splice site Het probably benign 08/02/2016
40 410272 APN Vmn2r27 0.076 IGL03130 6 124192317 D618G T C missense Het possibly damaging 0.816 08/02/2016
41 410301 APN Vmn2r91 0.057 IGL03130 17 18110111 T A splice site Het probably benign 08/02/2016
42 410281 APN Vti1a 0.000 IGL03130 19 55391847 Y143H T C missense Het probably damaging 1.000 phenotype 08/02/2016
43 410299 APN Zfand4 0.108 IGL03130 6 116273659 Y17N T A missense Het probably damaging 0.993 08/02/2016
44 410300 APN Zfp729a 0.062 IGL03130 13 67619642 T C intron 18005 bp Het probably null 08/02/2016
45 410286 APN Zfp827 0.914 IGL03130 8 79060957 T251A A G missense Het probably damaging 0.999 08/02/2016
[records 1 to 45 of 45]