Incidental Mutations

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

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 90183 APN 1700016C15Rik IGL01542 G1 1 177743384 T95A A G missense Het possibly damaging 0.944 12/03/2013
2 278561 APN Arap3 0.781 IGL01542 G1 18 37990836 R377C G A missense Het probably damaging 0.977 phenotype 04/16/2015
3 90184 APN Arhgap20 0.377 IGL01542 G1 9 51838887 M316V A G missense Het probably benign 0.000 phenotype 12/03/2013
4 90191 APN Chd7 0.951 IGL01542 G1 4 8859285 N2458K T G missense Het possibly damaging 0.712 phenotype 12/03/2013
5 90187 APN Clock 0.680 IGL01542 G1 5 76231475 E538G T C missense Het possibly damaging 0.820 phenotype 12/03/2013
6 90195 APN Clpb 0.912 IGL01542 G1 7 101787505 V596I G A missense Het probably damaging 0.979 phenotype 12/03/2013
7 90201 APN Col9a3 0.241 IGL01542 G1 2 180609316 T C splice site Het probably benign phenotype 12/03/2013
8 90204 APN D130043K22Rik 0.000 IGL01542 G1 13 24876037 G A splice site 5 bp Het probably null phenotype 12/03/2013
9 90202 APN Drd4 0.078 IGL01542 G1 7 141293831 T C unclassified Het probably benign phenotype 12/03/2013
10 90196 APN Fam228b 0.082 IGL01542 G1 12 4763055 I105N A T missense Het probably damaging 1.000 12/03/2013
11 90200 APN Gm20939 0.088 IGL01542 G1 17 94874293 A T splice site Het probably benign 12/03/2013
12 90180 APN Gm4952 0.062 IGL01542 G1 19 12618407 T54A A G missense Het possibly damaging 0.763 12/03/2013
13 90197 APN Hbs1l 0.000 IGL01542 G1 10 21307756 V132A T C missense Het probably benign 0.026 phenotype 12/03/2013
14 90194 APN Kpna2 0.935 IGL01542 G1 11 106991201 E266D T A missense Het probably benign 0.014 phenotype 12/03/2013
15 90185 APN Lars 1.000 IGL01542 G1 18 42214827 E977G T C missense Het probably benign 0.086 phenotype 12/03/2013
16 90198 APN Lrrn4 0.071 IGL01542 G1 2 132879472 T142A T C missense Het probably benign 0.000 phenotype 12/03/2013
17 90182 APN Myo19 0.145 IGL01542 G1 11 84909546 L919P T C missense Het probably damaging 0.961 12/03/2013
18 90188 APN Nhlrc1 0.270 IGL01542 G1 13 47014131 F217I A T missense Het probably damaging 0.972 phenotype 12/03/2013
19 90186 APN Olfr1495 0.123 IGL01542 G1 19 13768537 F65S T C missense Het probably damaging 0.999 phenotype 12/03/2013
20 90181 APN Plch1 0.167 IGL01542 G1 3 63731649 I468V T C missense Het probably damaging 0.994 phenotype 12/03/2013
21 90203 APN Rergl 0.088 IGL01542 G1 6 139493498 T A critical splice acceptor site Het probably null 12/03/2013
22 90199 APN Sctr 0.065 IGL01542 G1 1 120044769 A G splice site Het probably benign phenotype 12/03/2013
23 90189 APN Sdhb 1.000 IGL01542 G1 4 140972967 V126A T C missense Het probably benign 0.000 phenotype 12/03/2013
24 90190 APN Smad3 0.000 IGL01542 G1 9 63655586 R214Q C T missense Het probably damaging 0.976 phenotype 12/03/2013
25 90178 APN Tdrd9 0.177 IGL01542 G1 12 112046989 M1219T T C missense Het possibly damaging 0.940 phenotype 12/03/2013
26 90193 APN Tmem167b 0.191 IGL01542 G1 3 108558906 N75K A T missense Het possibly damaging 0.816 12/03/2013
27 90192 APN Vmn2r83 0.099 IGL01542 G1 10 79479012 S365P T C missense Het probably benign 0.301 12/03/2013
28 90179 APN Vps16 0.964 IGL01542 G1 2 130438394 F153L T C missense Het probably damaging 0.967 phenotype 12/03/2013
[records 1 to 28 of 28]