Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
4 are Possibly Damaging.
15 are Probably Damaging.
10 are Probably Benign.
5 are Probably Null.
3 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 27859 APN Adamts17 0.074 IGL00950 G1 7 67120912 V923A T C missense Het possibly damaging 0.690 phenotype 04/17/2013
2 26687 APN Als2 0.872 IGL00950 G1 1 59215382 A272V G A missense Het probably benign 0.008 phenotype 04/17/2013
3 28571 APN Chrne 0.117 IGL00950 G1 11 70619157 C T unclassified Het probably benign phenotype 04/17/2013
4 27861 APN D430042O09Rik 0.000 IGL00950 G1 7 125843221 D767E T A missense Het probably benign 0.000 phenotype 04/17/2013
5 27860 APN Dhx34 0.349 IGL00950 G1 7 16199826 R947H C T missense Het probably damaging 1.000 phenotype 04/17/2013
6 26690 APN Dnah7b 0.166 IGL00950 G1 1 46214322 M1796L A T missense Het probably benign 0.067 04/17/2013
7 27660 APN Doxl2 0.000 IGL00950 G1 6 48978131 N635T A C missense Het possibly damaging 0.821 04/17/2013
8 26686 APN Dstyk 0.216 IGL00950 G1 1 132459988 T820I C T missense Het probably damaging 0.996 phenotype 04/17/2013
9 29171 APN Eif4g1 0.965 IGL00950 G1 16 20683628 K942E A G missense Het probably damaging 1.000 phenotype 04/17/2013
10 26946 APN Fbn1 0.877 IGL00950 G1 2 125358823 G1318E C T missense Het probably damaging 1.000 phenotype 04/17/2013
11 26945 APN Galnt5 0.000 IGL00950 G1 2 57999132 V248A T C missense Het probably benign 0.001 phenotype 04/17/2013
12 28877 APN Gcnt4 0.080 IGL00950 G1 13 96946556 Y120C A G missense Het probably damaging 1.000 phenotype 04/17/2013
13 26948 APN Gdf5 0.441 IGL00950 G1 2 155941706 V442A A G missense Het probably damaging 0.999 phenotype 04/17/2013
14 29304 APN H2-Q4 0.062 IGL00950 G1 17 35382858 D232A A C missense Het probably damaging 1.000 phenotype 04/17/2013
15 278107 APN Hnrnpm 1.000 IGL00950 G1 17 33649902 R517L C A missense Het probably damaging 0.988 phenotype 04/16/2015
16 27465 APN Htt 1.000 IGL00950 G1 5 34891441 I2423V A G missense Het probably benign 0.000 phenotype 04/17/2013
17 28572 APN Itk 0.150 IGL00950 G1 11 46367896 I60F T A missense Het probably damaging 1.000 phenotype 04/17/2013
18 27862 APN Izumo1 0.000 IGL00950 G1 7 45622871 C25* T A nonsense Het probably null phenotype 04/17/2013
19 26689 APN Lamc1 1.000 IGL00950 G1 1 153240495 P980H G T missense Het probably damaging 1.000 phenotype 04/17/2013
20 27464 APN Ncor2 1.000 IGL00950 G1 5 125086890 R367L C A missense Het unknown phenotype 04/17/2013
21 29430 APN Pcdhb17 0.061 IGL00950 G1 18 37486006 A T unclassified Het probably null phenotype 04/17/2013
22 28207 APN Rnf123 0.256 IGL00950 G1 9 108067395 C A critical splice donor site 1 bp Het probably null phenotype 04/17/2013
23 28206 APN Sh3bgrl2 0.088 IGL00950 G1 9 83577490 F34I T A missense Het probably damaging 0.999 04/17/2013
24 29080 APN Sharpin 0.441 IGL00950 G1 15 76348224 E171G T C missense Het probably damaging 0.988 phenotype 04/17/2013
25 29524 APN Slc22a30 0.087 IGL00950 G1 19 8335788 D544E A T missense Het probably benign 0.286 04/17/2013
26 28573 APN Slc36a1 0.137 IGL00950 G1 11 55226128 C328R T C missense Het probably damaging 1.000 phenotype 04/17/2013
27 28761 APN Sntg2 0.076 IGL00950 G1 12 30312681 T C splice site Het probably benign phenotype 04/17/2013
28 26688 APN Sox13 0.000 IGL00950 G1 1 133387106 V272A A G missense Het probably benign 0.018 phenotype 04/17/2013
29 28366 APN Sppl2b 0.842 IGL00950 G1 10 80864094 L37R T G missense Het probably damaging 1.000 phenotype 04/17/2013
30 27129 APN Strip1 0.963 IGL00950 G1 3 107621445 S390C T A missense Het probably damaging 0.987 phenotype 04/17/2013
31 28368 APN Stxbp5 1.000 IGL00950 G1 10 9808602 T A splice site Het probably benign phenotype 04/17/2013
32 28964 APN Supt16 0.966 IGL00950 G1 14 52161798 E1008G T C missense Het possibly damaging 0.719 phenotype 04/17/2013
33 27858 APN Vmn1r174 0.053 IGL00950 G1 7 23754486 H192Q C A missense Het possibly damaging 0.956 04/17/2013
34 28367 APN Vsir 0.000 IGL00950 G1 10 60364284 Q154* C T nonsense Het probably null phenotype 04/17/2013
35 26947 APN Xrn2 0.962 IGL00950 G1 2 147028146 R252* A T nonsense Het probably null phenotype 04/17/2013
[records 1 to 35 of 35]