Incidental Mutations

33 incidental mutations are currently displayed, and affect 32 genes.
6 are Possibly Damaging.
14 are Probably Damaging.
9 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 33 of 33] 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 28353 APN 4933416C03Rik 0.150 IGL00942 G1 10 116113436 S62P A G missense Het possibly damaging 0.910 phenotype 04/17/2013
2 27452 APN Arap2 0.228 IGL00942 G1 5 62698389 L568* A C nonsense Het probably null phenotype 04/17/2013
3 26927 APN Arfgef2 0.332 IGL00942 G1 2 166885853 V1574M G A missense Het probably damaging 1.000 phenotype 04/17/2013
4 28193 APN Arhgef12 0.855 IGL00942 G1 9 42982000 R969H C T missense Het probably damaging 1.000 phenotype 04/17/2013
5 28556 APN Cacng1 0.145 IGL00942 G1 11 107704369 F127L A T missense Het probably benign 0.000 phenotype 04/17/2013
6 29289 APN Cntnap5c 0.119 IGL00942 G1 17 57769598 V10A T C missense Het probably benign 0.029 04/17/2013
7 29517 APN Crtac1 0.224 IGL00942 G1 19 42323794 D160A T G missense Het probably damaging 1.000 phenotype 04/17/2013
8 29071 APN Csmd3 0.848 IGL00942 G1 15 47847106 C T critical splice donor site 1 bp Het probably null 04/17/2013
9 27275 APN Grin3a 0.000 IGL00942 G1 4 49770589 F728L A G missense Het probably damaging 0.995 phenotype 04/17/2013
10 28864 APN Hecw1 0.137 IGL00942 G1 13 14340740 C T splice site Het probably benign 04/17/2013
11 28863 APN Hist1h3a IGL00942 G1 13 23761938 T C unclassified Het probably benign phenotype 04/17/2013
12 28354 APN Iyd 0.106 IGL00942 G1 10 3554070 C239F C T missense Het probably damaging 1.000 phenotype 04/17/2013
13 26926 APN Madd 1.000 IGL00942 G1 2 91170578 V486A A G missense Het probably damaging 0.999 phenotype 04/17/2013
14 27274 APN Map3k7 1.000 IGL00942 G1 4 32019539 D533G A G missense Het probably damaging 0.995 phenotype 04/17/2013
15 28355 APN Matk 0.000 IGL00942 G1 10 81258294 D20G A G missense Het probably benign 0.000 phenotype 04/17/2013
16 27845 APN Mphosph10 0.912 IGL00942 G1 7 64389755 S156P A G missense Het probably benign 0.005 phenotype 04/17/2013
17 28555 APN Mtif2 0.922 IGL00942 G1 11 29538753 E356K G A missense Het probably damaging 1.000 phenotype 04/17/2013
18 29293 APN Ndufb10 0.557 IGL00942 G1 17 24724184 T C splice site 3 bp Het probably null 04/17/2013
19 27276 APN Nipal3 0.123 IGL00942 G1 4 135468593 L233Q A T missense Het possibly damaging 0.896 phenotype 04/17/2013
20 28192 APN Olfr860 0.028 IGL00942 G1 9 19846259 Y120C T C missense Het probably damaging 1.000 phenotype 04/17/2013
21 29291 APN Prss32 0.115 IGL00942 G1 17 23859160 C273* T A nonsense Het probably null 04/17/2013
22 28194 APN Prtg 0.434 IGL00942 G1 9 72892340 S807P T C missense Het possibly damaging 0.820 phenotype 04/17/2013
23 27843 APN Ric3 0.088 IGL00942 G1 7 109054412 E157D T G missense Het probably damaging 1.000 phenotype 04/17/2013
24 27844 APN Ric3 0.088 IGL00942 G1 7 109054413 E157V T A missense Het probably damaging 1.000 phenotype 04/17/2013
25 26670 APN Slc16a14 0.169 IGL00942 G1 1 84922871 T131I G A missense Het probably damaging 0.986 04/17/2013
26 26928 APN Slc1a2 0.368 IGL00942 G1 2 102739814 N137Y A T missense Het probably damaging 0.996 phenotype 04/17/2013
27 29290 APN Slc25a27 0.145 IGL00942 G1 17 43664089 I94V T C missense Het probably benign 0.006 phenotype 04/17/2013
28 27646 APN Slco1a1 0.147 IGL00942 G1 6 141946628 T4I G A missense Het probably benign 0.005 phenotype 04/17/2013
29 28862 APN Slf1 0.000 IGL00942 G1 13 77043947 F923I A T missense Het possibly damaging 0.951 phenotype 04/17/2013
30 29070 APN Ttll12 0.075 IGL00942 G1 15 83582448 V306G A C missense Het possibly damaging 0.652 04/17/2013
31 27846 APN Tulp2 0.134 IGL00942 G1 7 45516268 V97I G A missense Het possibly damaging 0.871 phenotype 04/17/2013
32 27847 APN Vmn2r65 0.115 IGL00942 G1 7 84943553 Q482P T G missense Het probably damaging 0.992 04/17/2013
33 29292 APN Wdr24 0.912 IGL00942 G1 17 25826621 N443K T A missense Het probably benign 0.196 04/17/2013
[records 1 to 33 of 33]