Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
5 are Possibly Damaging.
17 are Probably Damaging.
12 are Probably Benign.
5 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 41 of 41] 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 105102 APN 1700088E04Rik 0.000 IGL01721 G1 15 79139253 M51V T C missense Het possibly damaging 0.878 01/21/2014
2 105125 APN Acad8 0.111 IGL01721 G1 9 26992267 A G splice site Het probably benign phenotype 01/21/2014
3 105109 APN Atp2a2 1.000 IGL01721 G1 5 122500792 V53A A G missense Het possibly damaging 0.889 phenotype 01/21/2014
4 105089 APN Bicra 0.139 IGL01721 G1 7 15988699 T298A T C missense Het probably benign 0.000 01/21/2014
5 105115 APN Ccdc185 0.072 IGL01721 G1 1 182748978 E49K C T missense Het possibly damaging 0.528 01/21/2014
6 105097 APN Cfhr2 0.063 IGL01721 G1 1 139813614 S208P A G missense Het probably benign 0.005 01/21/2014
7 105108 APN Chd1 0.000 IGL01721 G1 17 15770168 Y1661H T C missense Het probably damaging 0.999 phenotype 01/21/2014
8 105113 APN Cntnap5a 0.000 IGL01721 G1 1 116157637 H435R A G missense Het probably benign 0.000 phenotype 01/21/2014
9 105121 APN Cog8 0.143 IGL01721 G1 8 107054065 V187A A G missense Het probably benign 0.227 phenotype 01/21/2014
10 105096 APN Col24a1 0.000 IGL01721 G1 3 145538567 H1532R A G missense Het probably benign 0.264 phenotype 01/21/2014
11 105098 APN Dpp6 0.098 IGL01721 G1 5 27631520 Y336C A G missense Het probably damaging 1.000 phenotype 01/21/2014
12 105111 APN Drosha 0.957 IGL01721 G1 15 12846112 Y444* T A nonsense Het probably null phenotype 01/21/2014
13 105095 APN Egf 0.000 IGL01721 G1 3 129697722 C374* A T nonsense Het probably null phenotype 01/21/2014
14 105106 APN Eif2b3 1.000 IGL01721 G1 4 117058804 H203Y C T missense Het probably damaging 1.000 phenotype 01/21/2014
15 105092 APN Erbb4 1.000 IGL01721 G1 1 68254563 V723A A G missense Het possibly damaging 0.462 phenotype 01/21/2014
16 105107 APN Fbxo21 0.245 IGL01721 G1 5 117988790 I202T T C missense Het probably benign 0.041 phenotype 01/21/2014
17 105088 APN Gbp6 IGL01721 G1 5 105274207 M544V T C missense Het probably benign 0.011 01/21/2014
18 105116 APN Gm10750 0.073 IGL01721 G1 2 149016044 T96A T C missense Het unknown 01/21/2014
19 105112 APN Gm1840 0.897 IGL01721 G1 8 5639896 A T exon Het noncoding transcript 01/21/2014
20 105124 APN Gm8232 IGL01721 G1 14 44437183 A T splice site 3 bp Het probably null 01/21/2014
21 105090 APN Gsdma3 0.076 IGL01721 G1 11 98637956 V412A T C missense Het possibly damaging 0.946 phenotype 01/21/2014
22 105118 APN Hs6st1 0.809 IGL01721 G1 1 36068935 H93L A T missense Het probably damaging 0.998 phenotype 01/21/2014
23 105105 APN Hsf2 0.000 IGL01721 G1 10 57496181 E77K G A missense Het probably benign 0.125 phenotype 01/21/2014
24 105128 APN Ing3 0.961 IGL01721 G1 6 21968880 T A splice site Het probably benign phenotype 01/21/2014
25 105110 APN Ints6 1.000 IGL01721 G1 14 62713739 I280M T C missense Het probably damaging 0.959 phenotype 01/21/2014
26 105126 APN Kazn 0.191 IGL01721 G1 4 142159043 C A critical splice donor site 1 bp Het probably null phenotype 01/21/2014
27 105114 APN Klhl20 0.222 IGL01721 G1 1 161095587 Y13C T C missense Het probably damaging 1.000 phenotype 01/21/2014
28 105122 APN Krtap26-1 0.073 IGL01721 G1 16 88647172 P187L G A missense Het probably damaging 1.000 01/21/2014
29 105123 APN Mga 0.926 IGL01721 G1 2 119935239 I1329K T A missense Het probably damaging 1.000 phenotype 01/21/2014
30 105104 APN Mindy4 0.092 IGL01721 G1 6 55223999 D223G A G missense Het probably damaging 1.000 01/21/2014
31 105091 APN Ncor2 1.000 IGL01721 G1 5 125050937 E124G T C missense Het probably damaging 0.996 phenotype 01/21/2014
32 105127 APN Nfat5 0.915 IGL01721 G1 8 107344979 G A critical splice donor site 1 bp Het probably null phenotype 01/21/2014
33 105093 APN Nkain1 0.234 IGL01721 G1 4 130532134 F184L A G missense Het probably benign 0.004 phenotype 01/21/2014
34 105101 APN Olfr1061 0.074 IGL01721 G1 2 86413333 T240A T C missense Het probably damaging 1.000 phenotype 01/21/2014
35 105120 APN Rars 0.967 IGL01721 G1 11 35828664 F110L A T missense Het probably damaging 0.999 phenotype 01/21/2014
36 105094 APN Rfx6 1.000 IGL01721 G1 10 51723077 K509N A C missense Het probably damaging 0.999 phenotype 01/21/2014
37 105117 APN Serpinb2 0.000 IGL01721 G1 1 107515603 L44P T C missense Het probably damaging 0.999 phenotype 01/21/2014
38 105099 APN Sin3a 1.000 IGL01721 G1 9 57095325 R167Q G A missense Het probably damaging 1.000 phenotype 01/21/2014
39 105119 APN Sos2 0.000 IGL01721 G1 12 69603867 T809S T A missense Het probably damaging 0.988 phenotype 01/21/2014
40 105100 APN Stard9 0.200 IGL01721 G1 2 120703330 E3356G A G missense Het probably damaging 1.000 01/21/2014
41 105103 APN Vmn1r52 0.072 IGL01721 G1 6 90178923 T70A A G missense Het probably benign 0.000 01/21/2014
[records 1 to 41 of 41]