Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
3 are Possibly Damaging.
13 are Probably Damaging.
8 are Probably Benign.
3 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 27 of 27] 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 324125 UTSW Atxn7l2 0.318 R4319 G1 225 Y 3 108205832 D218E A T missense Het probably damaging 1.000 0.647 06/24/2015
2 324123 UTSW Bahd1 0.000 R4319 G1 225 Y 2 118916406 P169S C T missense Het probably damaging 0.999 0.066 phenotype 06/24/2015
3 324129 UTSW Cacna1c 0.376 R4319 G1 225 Y 6 118654369 I1148S A C missense Het probably damaging 1.000 0.315 phenotype 06/24/2015
4 377764 UTSW Ccdc178 0.000 R4319 G1 225 Y 18 22033543 K530* T A nonsense Het probably null 0.972 04/01/2016
5 324142 UTSW Ccdc191 0.132 R4319 G1 225 Y 16 43947509 E624G A G missense Het probably damaging 1.000 0.105 06/24/2015
6 324136 UTSW Cep290 0.927 R4319 G1 225 Y 10 100539047 H1385P A C missense Het probably benign 0.092 0.090 phenotype 06/24/2015
7 324141 UTSW Chrd 1.000 R4319 G1 225 Y 16 20737048 H545R A G missense Het probably damaging 0.994 0.391 phenotype 06/24/2015
8 324139 UTSW Dgkb 0.231 R4319 G1 225 Y 12 38438599 I655V A G missense Het probably damaging 0.999 0.295 phenotype 06/24/2015
9 324130 UTSW Gm15448 0.052 R4319 G1 225 Y 7 3822755 S372P A G missense Het possibly damaging 0.461 0.179 06/24/2015
10 324128 UTSW Gm2663 0.143 R4319 G1 109 N 6 40997596 Q87K G T missense Het probably damaging 0.999 06/24/2015
11 324143 UTSW Itsn1 0.000 R4319 G1 191 Y 16 91818552 G A intron Het probably benign 0.187 phenotype 06/24/2015
12 324149 UTSW Kif11 1.000 R4319 G1 225 Y 19 37384585 V84A T C missense Het probably damaging 0.986 0.370 phenotype 06/24/2015
13 324135 UTSW Klf2 1.000 R4319 G1 157 Y 8 72320161 T270A A G missense Het probably benign 0.299 0.093 phenotype 06/24/2015
14 324145 UTSW Lemd2 1.000 R4319 G1 225 Y 17 27201677 M254T A G missense Het possibly damaging 0.871 0.082 phenotype 06/24/2015
15 324144 UTSW Luc7l 0.222 R4319 G1 225 Y 17 26277619 A T utr 3 prime Het probably benign 0.120 phenotype 06/24/2015
16 324140 UTSW Mapk11 0.000 R4319 G1 225 Y 15 89146743 E71G T C missense Het probably damaging 1.000 0.884 phenotype 06/24/2015
17 324127 UTSW Mcoln2 0.084 R4319 G1 225 Y 3 146150011 G A splice site 5 bp Het probably null 0.976 phenotype 06/24/2015
18 324137 UTSW Olfr1392 0.071 R4319 G1 225 Y 11 49293676 M118I G A missense Het probably damaging 0.999 0.152 phenotype 06/24/2015
19 324124 UTSW Pygb 0.191 R4319 G1 225 Y 2 150815614 G T splice site Het probably benign phenotype 06/24/2015
20 324122 UTSW Rufy4 0.263 R4319 G1 225 Y 1 74147663 C537R T C missense Het probably damaging 0.988 0.860 06/24/2015
21 324133 UTSW Sox6 1.000 R4319 G1 225 Y 7 115580563 A G critical splice donor site 2 bp Het probably null 0.949 phenotype 06/24/2015
22 324132 UTSW Spty2d1 0.914 R4319 G1 225 Y 7 46998135 S349G T C missense Het probably damaging 0.989 0.064 06/24/2015
23 324148 UTSW Srbd1 0.960 R4319 G1 225 Y 17 86051150 V657D A T missense Het probably damaging 0.999 0.647 06/24/2015
24 324147 UTSW Tspo2 0.063 R4319 G1 185 Y 17 48449843 G T intron Het probably benign 0.090 06/24/2015
25 324134 UTSW Ufsp2 1.000 R4319 G1 225 Y 8 45995627 T422A A G missense Het possibly damaging 0.946 0.143 phenotype 06/24/2015
26 324131 UTSW Vmn2r63 0.072 R4319 G1 225 Y 7 42926982 F469S A G missense Het probably benign 0.040 0.090 06/24/2015
27 324146 UTSW Wdr46 0.969 R4319 G1 205 Y 17 33940744 T3A A G missense Het probably benign 0.044 0.069 06/24/2015
[records 1 to 27 of 27]