Incidental Mutations

40 incidental mutations are currently displayed, and affect 40 genes.
3 are Possibly Damaging.
19 are Probably Damaging.
14 are Probably Benign.
4 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 40 of 40] 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 360042 APN Adam2 0.000 IGL02798 14 66040275 C514S A T missense Het probably damaging 1.000 phenotype 12/18/2015
2 360031 APN Alcam 0.437 IGL02798 16 52305639 I105T A G missense Het probably damaging 0.998 phenotype 12/18/2015
3 360066 APN Arhgef10l 0.113 IGL02798 4 140565130 A T critical splice donor site 2 bp Het probably null phenotype 12/18/2015
4 360032 APN Arhgef17 0.000 IGL02798 7 100929626 V705A A G missense Het probably benign 0.005 12/18/2015
5 360050 APN C87436 0.429 IGL02798 6 86446202 C253S T A missense Het probably benign 0.013 12/18/2015
6 360046 APN Cbx7 0.146 IGL02798 15 79918399 T226A T C missense Het probably damaging 0.999 phenotype 12/18/2015
7 360051 APN Cdh20 0.320 IGL02798 1 104947465 I324T T C missense Het probably damaging 0.966 phenotype 12/18/2015
8 360033 APN Celsr3 1.000 IGL02798 9 108843575 H2608L A T missense Het probably damaging 1.000 phenotype 12/18/2015
9 360065 APN Cramp1l 0.000 IGL02798 17 24968920 A G splice site Het probably benign phenotype 12/18/2015
10 360055 APN Ddx25 0.223 IGL02798 9 35551397 C231R A G missense Het probably damaging 1.000 phenotype 12/18/2015
11 360061 APN Emilin2 0.083 IGL02798 17 71256695 A G splice site Het probably benign phenotype 12/18/2015
12 360048 APN Fam46a 0.316 IGL02798 9 85324884 V287E A T missense Het probably damaging 0.997 phenotype 12/18/2015
13 360063 APN Hip1r 0.000 IGL02798 5 123994712 T C unclassified Het probably benign phenotype 12/18/2015
14 360049 APN Insrr 0.258 IGL02798 3 87810517 P842S C T missense Het probably damaging 1.000 phenotype 12/18/2015
15 360062 APN Lama1 1.000 IGL02798 17 67795191 G T splice site Het probably benign phenotype 12/18/2015
16 360060 APN Lig3 1.000 IGL02798 11 82795705 T C splice site Het probably benign phenotype 12/18/2015
17 360058 APN Lrp4 0.612 IGL02798 2 91476710 T392K C A missense Het probably benign 0.019 phenotype 12/18/2015
18 360038 APN Msl2 0.956 IGL02798 9 101075377 R33S G T missense Het probably benign 0.057 12/18/2015
19 360057 APN Nrde2 1.000 IGL02798 12 100143822 K317* T A nonsense Het probably null 12/18/2015
20 360044 APN Nub1 0.890 IGL02798 5 24692814 A42D C A missense Het probably damaging 0.998 phenotype 12/18/2015
21 360035 APN Obox2 0.735 IGL02798 7 15396882 V13A T C missense Het possibly damaging 0.853 12/18/2015
22 360027 APN Olfr1341 0.104 IGL02798 4 118709499 F31L T C missense Het probably damaging 0.972 phenotype 12/18/2015
23 360039 APN Olfr202 0.062 IGL02798 16 59284115 C127* A T nonsense Het probably null phenotype 12/18/2015
24 360056 APN Olfr729 0.143 IGL02798 14 50148378 K165N T A missense Het probably benign 0.000 phenotype 12/18/2015
25 360053 APN Phkb 0.787 IGL02798 8 86043777 Y892H T C missense Het probably benign 0.000 phenotype 12/18/2015
26 360037 APN Ptdss1 0.000 IGL02798 13 66976760 Y341C A G missense Het probably damaging 1.000 phenotype 12/18/2015
27 360034 APN Ripor2 0.156 IGL02798 13 24674666 D147V A T missense Het probably damaging 0.993 0.915 phenotype 12/18/2015
28 360029 APN Scn7a 0.110 IGL02798 2 66713875 D424G T C missense Het probably benign 0.002 phenotype 12/18/2015
29 360047 APN Scn9a 1.000 IGL02798 2 66540559 R559Q C T missense Het possibly damaging 0.516 phenotype 12/18/2015
30 360045 APN Sctr 0.084 IGL02798 1 120022180 C33Y G A missense Het probably damaging 1.000 phenotype 12/18/2015
31 360036 APN Sh2b2 0.935 IGL02798 5 136221963 A419E G T missense Het probably damaging 1.000 phenotype 12/18/2015
32 360030 APN Slc22a30 0.087 IGL02798 19 8370085 M317K A T missense Het probably damaging 0.957 12/18/2015
33 360054 APN Slc39a4 1.000 IGL02798 15 76615182 S178G T C missense Het probably benign 0.044 phenotype 12/18/2015
34 360043 APN Slc7a12 0.072 IGL02798 3 14481157 C121S T A missense Het probably damaging 1.000 12/18/2015
35 360028 APN Slmap 1.000 IGL02798 14 26470378 S148G T C missense Het possibly damaging 0.875 phenotype 12/18/2015
36 360052 APN Tktl2 0.371 IGL02798 8 66513311 K507R A G missense Het probably benign 0.058 12/18/2015
37 360041 APN Ttn 1.000 IGL02798 2 76755863 K21841N T G missense Het probably damaging 0.993 phenotype 12/18/2015
38 360040 APN Ugcg 1.000 IGL02798 4 59220346 Y380H T C missense Het probably damaging 0.995 phenotype 12/18/2015
39 360059 APN Zfp106 0.000 IGL02798 2 120510510 T1840A T C missense Het probably damaging 1.000 phenotype 12/18/2015
40 360064 APN Zmynd8 1.000 IGL02798 2 165852150 T C critical splice acceptor site Het probably null phenotype 12/18/2015
[records 1 to 40 of 40]