Incidental Mutations

29 incidental mutations are currently displayed, and affect 28 genes.
7 are Possibly Damaging.
8 are Probably Damaging.
9 are Probably Benign.
2 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 420829 APN Bbs9 0.580 IGL03385 9 22643748 T444A A G missense Het probably benign 0.192 phenotype 08/02/2016
2 420835 APN Cdh7 0.139 IGL03385 1 110065786 T324A A G missense Het possibly damaging 0.901 phenotype 08/02/2016
3 420830 APN Col14a1 0.000 IGL03385 15 55410204 T723K C A missense Het unknown phenotype 08/02/2016
4 420854 APN Col14a1 0.000 IGL03385 15 55471708 G1513S G A missense Het unknown phenotype 08/02/2016
5 420847 APN Col1a2 0.000 IGL03385 6 4539612 N1293K C A missense Het unknown phenotype 08/02/2016
6 420848 APN Ctdp1 0.962 IGL03385 18 80449918 D454G T C missense Het probably damaging 0.995 phenotype 08/02/2016
7 420837 APN Fut2 0.000 IGL03385 7 45650769 G193E C T missense Het possibly damaging 0.939 phenotype 08/02/2016
8 420841 APN G3bp2 0.742 IGL03385 5 92068395 V94A A G missense Het probably damaging 0.998 08/02/2016
9 420845 APN Gm973 0.132 IGL03385 1 59582470 S590G A G missense Het probably benign 0.139 08/02/2016
10 420853 APN Gon4l 0.645 IGL03385 3 88907543 T1940S A T missense Het probably benign 0.100 phenotype 08/02/2016
11 420839 APN Itk 0.449 IGL03385 11 46331861 Q594* G A nonsense Het probably null phenotype 08/02/2016
12 420832 APN Kcnc2 0.161 IGL03385 10 112455786 C293Y G A missense Het probably damaging 1.000 phenotype 08/02/2016
13 420844 APN Krit1 1.000 IGL03385 5 3807452 I86V A G missense Het possibly damaging 0.511 phenotype 08/02/2016
14 420842 APN Lyst 0.431 IGL03385 13 13656980 L1663* T A nonsense Het probably null phenotype 08/02/2016
15 420843 APN Moxd2 0.059 IGL03385 6 40879018 T546A T C missense Het probably damaging 0.999 08/02/2016
16 420836 APN Myo7b 0.500 IGL03385 18 31989577 Q717K G T missense Het probably benign 0.001 phenotype 08/02/2016
17 420840 APN Olfr1368 0.072 IGL03385 13 21142487 V190A A G missense Het probably benign 0.009 phenotype 08/02/2016
18 420828 APN Olfr435 0.064 IGL03385 6 43201980 V112A T C missense Het probably benign 0.202 phenotype 08/02/2016
19 420834 APN Ostm1 0.361 IGL03385 10 42698144 N123H A C missense Het probably damaging 1.000 phenotype 08/02/2016
20 420846 APN Pcdh10 0.308 IGL03385 3 45381512 S754R A C missense Het possibly damaging 0.773 phenotype 08/02/2016
21 420851 APN Pomt2 1.000 IGL03385 12 87116556 L613Q A T missense Het probably damaging 0.999 phenotype 08/02/2016
22 420833 APN Samd9l 0.000 IGL03385 6 3376208 N351I T A missense Het probably damaging 0.988 phenotype 08/02/2016
23 420855 APN Serpinb9 0.289 IGL03385 13 33007996 T C splice site Het probably benign phenotype 08/02/2016
24 420856 APN Slc12a4 0.265 IGL03385 8 105950864 T A unclassified Het probably benign phenotype 08/02/2016
25 420831 APN Smgc 0.062 IGL03385 15 91841978 H42Q T A missense Het possibly damaging 0.663 08/02/2016
26 420849 APN Tor1a 1.000 IGL03385 2 30963727 V197A A G missense Het possibly damaging 0.832 phenotype 08/02/2016
27 420852 APN Ttc4 0.672 IGL03385 4 106668200 S246P A G missense Het probably benign 0.002 phenotype 08/02/2016
28 420850 APN Tti1 0.974 IGL03385 2 157993025 A1005V G A missense Het possibly damaging 0.862 08/02/2016
29 420838 APN Ugt3a2 0.030 IGL03385 15 9338738 I63F A T missense Het probably damaging 0.985 08/02/2016
[records 1 to 29 of 29]