Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
3 are Possibly Damaging.
13 are Probably Damaging.
17 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 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 302040 APN Aadacl4 0.072 IGL02648 4 144617822 A T critical splice acceptor site Het probably null 04/16/2015
2 302041 APN Acp4 0.107 IGL02648 7 44254990 A G unclassified Het probably benign phenotype 04/16/2015
3 302023 APN Adgrv1 0.000 IGL02648 13 81511619 M1997K A T missense Het probably benign 0.355 phenotype 04/16/2015
4 302011 APN Arhgdib 0.000 IGL02648 6 136933649 D38G T C missense Het probably damaging 1.000 phenotype 04/16/2015
5 302010 APN Bbox1 0.066 IGL02648 2 110305526 D36A T G missense Het probably damaging 1.000 phenotype 04/16/2015
6 302038 APN Cacna1c 0.397 IGL02648 6 118757496 K104R T C missense Het probably damaging 0.999 phenotype 04/16/2015
7 302024 APN Cacna1i 0.000 IGL02648 15 80298638 C75Y G A missense Het probably damaging 0.960 phenotype 04/16/2015
8 302009 APN Ccdc14 0.341 IGL02648 16 34697158 L70S T C missense Het probably damaging 0.998 04/16/2015
9 302021 APN Ccdc88a 1.000 IGL02648 11 29501051 V1580G T G missense Het probably benign 0.284 phenotype 04/16/2015
10 302022 APN Cdadc1 0.184 IGL02648 14 59586363 D227Y C A missense Het probably damaging 1.000 04/16/2015
11 302019 APN Chd3 0.000 IGL02648 11 69352150 Y1415C T C missense Het probably damaging 1.000 phenotype 04/16/2015
12 302025 APN Cngb3 0.100 IGL02648 4 19428489 N493S A G missense Het probably benign 0.001 phenotype 04/16/2015
13 302035 APN Dock10 0.612 IGL02648 1 80574123 Y665F T A missense Het probably damaging 0.999 phenotype 04/16/2015
14 302034 APN Gm10549 0.064 IGL02648 18 33464250 C A unclassified Het probably benign 04/16/2015
15 302012 APN Gm17677 0.083 IGL02648 9 35741109 M21L A T missense Het probably benign 0.135 04/16/2015
16 302033 APN Greb1 0.000 IGL02648 12 16708682 V678M C T missense Het probably damaging 0.998 phenotype 04/16/2015
17 302027 APN Gucy2c 0.000 IGL02648 6 136729213 R497* G A nonsense Het probably null phenotype 04/16/2015
18 302013 APN Itgad 0.084 IGL02648 7 128183374 T C intron Het probably benign phenotype 04/16/2015
19 302028 APN Lgr4 1.000 IGL02648 2 110012373 T877K C A missense Het probably damaging 1.000 phenotype 04/16/2015
20 302036 APN Lrig3 0.248 IGL02648 10 125966594 D40G A G missense Het probably benign 0.000 phenotype 04/16/2015
21 302039 APN Myo3b 0.000 IGL02648 2 70105372 T C splice site Het probably benign phenotype 04/16/2015
22 302032 APN Neb 0.832 IGL02648 2 52271081 Y2193H A G missense Het possibly damaging 0.791 phenotype 04/16/2015
23 302017 APN Olfr1270 0.101 IGL02648 2 90149353 I218F T A missense Het possibly damaging 0.613 phenotype 04/16/2015
24 302018 APN Olfr918 0.222 IGL02648 9 38673016 M143V T C missense Het probably benign 0.000 phenotype 04/16/2015
25 302030 APN Pard6b 0.429 IGL02648 2 168098927 Q278R A G missense Het probably benign 0.170 phenotype 04/16/2015
26 302016 APN Pkd2l1 0.108 IGL02648 19 44155536 Y366C T C missense Het possibly damaging 0.716 phenotype 04/16/2015
27 302007 APN Prl2c1 0.066 IGL02648 13 27857559 D188G A G missense Het probably benign 0.435 04/16/2015
28 302026 APN Prl3a1 0.082 IGL02648 13 27270235 M65I G T missense Het probably benign 0.005 04/16/2015
29 302008 APN Psg26 0.054 IGL02648 7 18482766 E49D T A missense Het probably benign 0.053 04/16/2015
30 302031 APN Rapgef3 0.174 IGL02648 15 97758392 R38W G A missense Het probably damaging 0.996 phenotype 04/16/2015
31 302029 APN Rrn3 1.000 IGL02648 16 13811589 F590L T C missense Het probably benign 0.000 phenotype 04/16/2015
32 302014 APN Serpina12 0.000 IGL02648 12 104038008 K122E T C missense Het probably benign 0.022 phenotype 04/16/2015
33 302020 APN Slc39a6 0.316 IGL02648 18 24582367 I699V T C missense Het probably damaging 0.997 phenotype 04/16/2015
34 302037 APN Tmem259 0.000 IGL02648 10 79977817 P443S G A missense Het probably damaging 1.000 04/16/2015
35 302015 APN Vmn1r75 0.059 IGL02648 7 11881164 F274L T A missense Het probably benign 0.040 04/16/2015
[records 1 to 35 of 35]