Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
6 are Possibly Damaging.
9 are Probably Damaging.
8 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 55834 UTSW Abcc9 0.129 R0588 G1 161 Y 6 142603061 K1299* T A nonsense Het probably null 0.972 phenotype 07/11/2013
2 55843 UTSW Adamts2 0.114 R0588 G1 225 Y 11 50776664 W476C G T missense Het probably damaging 1.000 0.621 phenotype 07/11/2013
3 55832 UTSW Ankrd13c 0.758 R0588 G1 225 Y 3 158005817 F525L T C missense Het probably damaging 1.000 0.658 07/11/2013
4 55841 UTSW Arg1 0.288 R0588 G1 183 Y 10 24920624 S102G T C missense Het probably damaging 1.000 0.546 phenotype 07/11/2013
5 55844 UTSW Atp2a3 0.165 R0588 G1 211 Y 11 72973024 D192V A T missense Het possibly damaging 0.785 0.179 phenotype 07/11/2013
6 55842 UTSW Cabin1 1.000 R0588 G1 214 Y 10 75745337 E385G T C missense Het possibly damaging 0.714 0.064 phenotype 07/11/2013
7 55848 UTSW Cacna1h 0.000 R0588 G1 225 Y 17 25387564 D1020E A T missense Het probably damaging 1.000 0.084 phenotype 07/11/2013
8 55835 UTSW Calcb 0.000 R0588 G1 102 Y 7 114720126 H48Y C T missense Het probably benign 0.046 0.090 07/11/2013
9 55839 UTSW Crtc1 0.471 R0588 G1 225 N 8 70439549 S4P A G missense Het probably damaging 0.994 phenotype 07/11/2013
10 55830 UTSW Dcaf6 0.000 R0588 G1 225 Y 1 165420223 I147T A G missense Het possibly damaging 0.889 0.916 07/11/2013
11 55837 UTSW Ears2 1.000 R0588 G1 160 Y 7 122044291 T C splice site Het probably benign phenotype 07/11/2013
12 55852 UTSW Fas 0.153 R0588 G1 225 Y 19 34327140 V267A T C missense Het probably damaging 0.993 0.717 phenotype 07/11/2013
13 55838 UTSW Fus 1.000 R0588 G1 225 Y 7 127985574 L84P T C missense Het probably damaging 0.985 0.647 phenotype 07/11/2013
14 55846 UTSW Fyb 0.000 R0588 G1 225 Y 15 6580459 V171A T C missense Het probably benign 0.032 0.090 phenotype 07/11/2013
15 55831 UTSW Gdap2 0.000 R0588 G1 138 Y 3 100170001 M1K T A start codon destroyed Het probably null 1.000 0.955 07/11/2013
16 55836 UTSW Gprc5b 0.424 R0588 G1 163 Y 7 118983995 Q217L T A missense Het probably benign 0.000 0.090 phenotype 07/11/2013
17 55833 UTSW Lrrc69 0.078 R0588 G1 225 Y 4 14704001 I273T A G missense Het possibly damaging 0.712 0.711 07/11/2013
18 55828 UTSW Map4k4 1.000 R0588 G1 225 Y 1 40004864 Q556K C A missense Het possibly damaging 0.931 0.070 phenotype 07/11/2013
19 55850 UTSW Npy6r 0.000 R0588 G1 225 Y 18 44275821 V103E T A missense Het possibly damaging 0.939 0.179 phenotype 07/11/2013
20 55851 UTSW Olfr1449 0.000 R0588 G1 225 Y 19 12934747 Y3C A G missense Het probably benign 0.001 0.090 phenotype 07/11/2013
21 55847 UTSW Shisa9 0.096 R0588 G1 225 Y 16 12267774 T416A A G missense Het probably damaging 0.993 0.095 phenotype 07/11/2013
22 55829 UTSW Slc26a9 0.885 R0588 G1 225 Y 1 131754011 C A splice site Het probably benign 0.090 phenotype 07/11/2013
23 55845 UTSW Sostdc1 0.555 R0588 G1 163 Y 12 36317021 G T splice site Het probably benign 0.090 phenotype 07/11/2013
24 55827 UTSW St18 0.000 R0588 G1 219 Y 1 6817738 F510L T A missense Het probably damaging 0.989 0.647 07/11/2013
25 55840 UTSW Zdhhc7 0.119 R0588 G1 190 Y 8 120083367 A G intron Het probably benign 0.090 07/11/2013
[records 1 to 25 of 25]