Incidental Mutations

37 incidental mutations are currently displayed, and affect 36 genes.
8 are Possibly Damaging.
15 are Probably Damaging.
10 are Probably Benign.
4 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 37 of 37] 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 52263 APN 1700016K19Rik 0.000 IGL01089 G1 11 76003337 E180G A G missense Het possibly damaging 0.819 06/21/2013
2 52667 APN Actr8 1.000 IGL01089 G1 14 29988335 L353S T C missense Het probably damaging 0.995 06/21/2013
3 53041 APN Adgrf2 0.000 IGL01089 G1 17 42710158 P592S G A missense Het probably damaging 1.000 phenotype 06/21/2013
4 278169 APN Aen 0.079 IGL01089 G1 7 78907302 M299I G A missense Het probably damaging 0.960 04/16/2015
5 53240 APN Afap1l2 0.098 IGL01089 G1 19 56913411 A C splice site Het probably null 06/21/2013
6 50231 APN Asnsd1 0.131 IGL01089 G1 1 53348277 P64S G A missense Het probably damaging 1.000 06/21/2013
7 51285 APN Bmt2 0.139 IGL01089 G1 6 13663271 M76T A G missense Het probably damaging 0.999 06/21/2013
8 50724 APN Clca3b 0.058 IGL01089 G1 3 144823522 V797D A T missense Het probably benign 0.000 06/21/2013
9 51744 APN Cog2 1.000 IGL01089 G1 8 124545243 S499P T C missense Het probably benign 0.002 phenotype 06/21/2013
10 50232 APN Cyp27a1 0.124 IGL01089 G1 1 74731938 Y94F A T missense Het possibly damaging 0.881 phenotype 06/21/2013
11 51490 APN D430042O09Rik 0.000 IGL01089 G1 7 125795313 E187G A G missense Het probably damaging 0.999 phenotype 06/21/2013
12 51288 APN D630045J12Rik 0.000 IGL01089 G1 6 38136963 S1765P A G missense Het probably benign 0.000 phenotype 06/21/2013
13 51743 APN Fam149a 0.000 IGL01089 G1 8 45348527 L519P A G missense Het possibly damaging 0.953 06/21/2013
14 52264 APN Fam171a2 0.107 IGL01089 G1 11 102437848 A695V G A missense Het possibly damaging 0.922 06/21/2013
15 51745 APN Fat1 1.000 IGL01089 G1 8 45017857 V1566E T A missense Het probably damaging 1.000 phenotype 06/21/2013
16 50234 APN Flvcr1 1.000 IGL01089 G1 1 191013390 N361H T G missense Het probably damaging 0.982 phenotype 06/21/2013
17 51896 APN Gm1110 0.078 IGL01089 G1 9 26881860 N540S T C missense Het probably benign 0.000 06/21/2013
18 52441 APN Kcns3 0.163 IGL01089 G1 12 11091571 T376S T A missense Het possibly damaging 0.924 phenotype 06/21/2013
19 52262 APN Krt32 0.080 IGL01089 G1 11 100087779 S150P A G missense Het probably benign 0.229 phenotype 06/21/2013
20 51286 APN Lrtm2 0.076 IGL01089 G1 6 119320792 R96Q C T missense Het possibly damaging 0.914 06/21/2013
21 52555 APN Mctp1 0.000 IGL01089 G1 13 77020798 E838G A G missense Het probably damaging 0.981 06/21/2013
22 51287 APN Mios 0.936 IGL01089 G1 6 8234363 T C critical splice donor site 2 bp Het probably null 06/21/2013
23 50470 APN Olfr338 0.052 IGL01089 G1 2 36377166 Y130F A T missense Het probably damaging 1.000 phenotype 06/21/2013
24 51895 APN Phldb1 0.106 IGL01089 G1 9 44707887 K167* T A nonsense Het probably null 06/21/2013
25 52788 APN Pkhd1l1 0.000 IGL01089 G1 15 44483869 A G splice site Het probably benign 06/21/2013
26 50879 APN Plaa 0.929 IGL01089 G1 4 94574047 V531A A G missense Het probably benign 0.000 phenotype 06/21/2013
27 50880 APN Psmb2 0.965 IGL01089 G1 4 126684206 Y59C A G missense Het probably damaging 1.000 phenotype 06/21/2013
28 52668 APN Ptprg 0.000 IGL01089 G1 14 12215286 H1091R A G missense Het probably damaging 0.970 phenotype 06/21/2013
29 50233 APN Rbm44 0.055 IGL01089 G1 1 91168697 V926D T A missense Het possibly damaging 0.608 phenotype 06/21/2013
30 51491 APN Rgma 0.217 IGL01089 G1 7 73409714 V189L G T missense Het possibly damaging 0.788 phenotype 06/21/2013
31 51492 APN Sbf2 0.552 IGL01089 G1 7 110348962 I1227K A T missense Het probably damaging 1.000 phenotype 06/21/2013
32 53042 APN Slc8a1 1.000 IGL01089 G1 17 81648281 T443A T C missense Het probably damaging 0.999 phenotype 06/21/2013
33 53043 APN Slc8a1 1.000 IGL01089 G1 17 81388881 V896A A G missense Het probably damaging 1.000 phenotype 06/21/2013
34 52787 APN Taf2 1.000 IGL01089 G1 15 55016581 M1120V T C missense Het probably benign 0.000 phenotype 06/21/2013
35 51080 APN Ugt2b34 0.110 IGL01089 G1 5 86906326 V199I C T missense Het probably benign 0.017 06/21/2013
36 50723 APN Unc5c 1.000 IGL01089 G1 3 141818202 C A splice site Het probably benign phenotype 06/21/2013
37 50235 APN Usp37 1.000 IGL01089 G1 1 74493046 R63* G A nonsense Het probably null phenotype 06/21/2013
[records 1 to 37 of 37]