Incidental Mutations

35 incidental mutations are currently displayed, and affect 34 genes.
5 are Possibly Damaging.
16 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 332234 APN 4930533K18Rik 0.125 IGL00499 G1 10 70875308 C A unclassified Het noncoding transcript 08/05/2015
2 5539 APN Abcb9 0.000 IGL00499 G1 5 124077238 D480G T C missense Het possibly damaging 0.901 phenotype 04/20/2012
3 5043 APN Adam26a 0.000 IGL00499 G1 8 43568859 N531K A T missense Het possibly damaging 0.755 phenotype 04/20/2012
4 332236 APN AW554918 0.062 IGL00499 G1 18 25420065 K542* A T nonsense Het probably null 08/05/2015
5 4174 APN Blk 0.000 IGL00499 G1 14 63380720 F246L A G missense Het probably damaging 1.000 phenotype 04/20/2012
6 5392 APN Camk1 0.000 IGL00499 G1 6 113336211 E292G T C missense Het probably benign 0.005 phenotype 04/20/2012
7 4624 APN Ccdc88a 1.000 IGL00499 G1 11 29499341 T261I C T missense Het probably benign 0.244 phenotype 04/20/2012
8 4672 APN Cep290 0.907 IGL00499 G1 10 100543327 Q57L A T missense Het probably damaging 0.999 phenotype 04/20/2012
9 5827 APN Cpsf1 0.969 IGL00499 G1 15 76600216 H688Q A T missense Het probably benign 0.271 phenotype 04/20/2012
10 6730 APN Cryz 0.156 IGL00499 G1 3 154604942 V13A T C missense Het possibly damaging 0.952 phenotype 04/20/2012
11 13432 APN Dst 0.330 IGL00499 G1 1 34290423 K6858R A G missense Het probably damaging 0.993 phenotype 12/06/2012
12 4946 APN Dync2h1 1.000 IGL00499 G1 9 7168700 V371E A T missense Het possibly damaging 0.948 phenotype 04/20/2012
13 6323 APN Eps8 0.319 IGL00499 G1 6 137522888 E181* C A nonsense Het probably null phenotype 04/20/2012
14 4610 APN Flt4 1.000 IGL00499 G1 11 49635261 I796T T C missense Het probably damaging 0.998 phenotype 04/20/2012
15 6887 APN Gmps 0.955 IGL00499 G1 3 64014367 N597S A G missense Het probably benign 0.000 phenotype 04/20/2012
16 7140 APN Itgav 1.000 IGL00499 G1 2 83802995 M1011K T A missense Het probably damaging 0.999 phenotype 04/20/2012
17 7011 APN Kif16b 1.000 IGL00499 G1 2 142857324 M112T A G missense Het probably damaging 1.000 phenotype 04/20/2012
18 332238 APN Lig1 1.000 IGL00499 G1 7 13298830 T C critical splice donor site 2 bp Het probably null phenotype 08/05/2015
19 3436 APN Lrrc30 0.000 IGL00499 G1 17 67632039 F182S A G missense Het probably damaging 0.999 04/20/2012
20 5907 APN Oxsm 1.000 IGL00499 G1 14 16242076 M231K A T missense Het probably damaging 1.000 phenotype 04/20/2012
21 6704 APN Pnisr 0.953 IGL00499 G1 4 21870407 T C critical splice donor site 2 bp Het probably null 04/20/2012
22 6882 APN Rsrc1 0.114 IGL00499 G1 3 67082600 A T intron Het probably benign phenotype 04/20/2012
23 332237 APN Setd1b 1.000 IGL00499 G1 5 123158747 A T unclassified Het probably benign phenotype 08/05/2015
24 6257 APN Tbx6 1.000 IGL00499 G1 7 126781529 Y8C A G missense Het probably damaging 0.996 phenotype 04/20/2012
25 6424 APN Tmem33 0.205 IGL00499 G1 5 67284195 Y196H T C missense Het probably damaging 1.000 04/20/2012
26 332235 APN Traf5 0.000 IGL00499 G1 1 192057174 D96G T C missense Het possibly damaging 0.947 phenotype 08/05/2015
27 4152 APN Tsc22d1 0.288 IGL00499 G1 14 76418917 D945E T A missense Het probably damaging 0.992 phenotype 04/20/2012
28 5946 APN Tubb2b 0.719 IGL00499 G1 13 34128346 I155V T C missense Het probably benign 0.001 phenotype 04/20/2012
29 6915 APN Usp13 0.000 IGL00499 G1 3 32881411 Y328N T A missense Het probably damaging 0.984 04/20/2012
30 5189 APN Usp17lc 1.000 IGL00499 G1 7 103418466 D323N G A missense Het probably damaging 0.998 phenotype 04/20/2012
31 5190 APN Usp17lc 1.000 IGL00499 G1 7 103418465 M322I G A missense Het probably damaging 1.000 phenotype 04/20/2012
32 6996 APN Zfp341 0.000 IGL00499 G1 2 154634231 T446I C T missense Het probably damaging 0.999 04/20/2012
33 3278 APN Zfp407 1.000 IGL00499 G1 18 84561752 L412P A G missense Het probably damaging 0.985 phenotype 04/20/2012
34 3386 APN Zfp521 0.930 IGL00499 G1 18 13939120 D21V T A missense Het probably benign 0.246 phenotype 04/20/2012
35 5114 APN Zranb1 0.896 IGL00499 G1 7 132982504 A G splice site Het probably benign phenotype 04/20/2012
[records 1 to 35 of 35]