Incidental Mutations

45 incidental mutations are currently displayed, and affect 45 genes.
6 are Possibly Damaging.
17 are Probably Damaging.
14 are Probably Benign.
8 are Probably Null.
2 create premature stop codons.
3 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 45 of 45] 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 522205 UTSW 1700029P11Rik 0.345 R6556 G1 225.01 N 15 81980738 D60G A G missense Het probably damaging 0.989 06/06/2018
2 522132 UTSW 2310035C23Rik 0.340 R6556 G1 225.01 N 1 105726440 F845I T A missense Het probably damaging 1.000 06/06/2018
3 522208 UTSW 4930539E08Rik 0.000 R6556 G1 225.01 N 17 28904611 D114V T A missense Het probably damaging 0.988 06/06/2018
4 522168 UTSW AF366264 0.626 R6556 G1 225.01 N 8 13837690 Q134* G A nonsense Het probably null 06/06/2018
5 522166 UTSW Atp2a1 1.000 R6556 G1 225.01 N 7 126450262 P536Q G T missense Het probably benign 0.372 phenotype 06/06/2018
6 522210 UTSW Cabyr 0.076 R6556 G1 225.01 N 18 12751016 S187T T A missense Het probably benign 0.074 0.064 phenotype 06/06/2018
7 522187 UTSW Camkk1 0.000 R6556 G1 225.01 N 11 73033870 N303I A T missense Het probably benign 0.319 phenotype 06/06/2018
8 522170 UTSW Cdh13 0.000 R6556 G1 225.01 N 8 118968187 P259S C T missense Het probably damaging 0.990 phenotype 06/06/2018
9 522212 UTSW Csnk1g3 0.000 R6556 G1 225.01 N 18 53930282 D255G A G missense Het possibly damaging 0.821 phenotype 06/06/2018
10 522160 UTSW Dennd5b 0.183 R6556 G1 225.01 N 6 149014251 A C splice site Het probably null phenotype 06/06/2018
11 522185 UTSW Dnajc14 0.000 R6556 G1 225.01 N 10 128814631 D528G A G missense Het probably benign 0.417 06/06/2018
12 522156 UTSW Edem1 0.194 R6556 G1 225.01 N 6 108854357 F593S T C missense Het probably benign 0.001 06/06/2018
13 522191 UTSW Erbb2 1.000 R6556 G1 225.01 N 11 98436082 D1106N G A missense Het possibly damaging 0.917 phenotype 06/06/2018
14 522218 UTSW Ermp1 0.000 R6556 G1 225.01 N 19 29612921 M794V T C missense Het possibly damaging 0.910 phenotype 06/06/2018
15 522200 UTSW Fam208a 1.000 R6556 G1 187.01 N 14 27429258 Y64D T G missense Het probably benign 0.000 phenotype 06/06/2018
16 522144 UTSW Fam214b 0.311 R6556 G1 225.01 N 4 43033896 R460H C T missense Het probably damaging 0.960 06/06/2018
17 522148 UTSW Fip1l1 0.961 R6556 G1 225.01 N 5 74547177 T A critical splice donor site 2 bp Het probably null 06/06/2018
18 522193 UTSW Gm11639 0.099 R6556 G1 225.01 N 11 105008251 N4343S A G missense Het probably null 0.026 06/06/2018
19 522154 UTSW Gm20730 0.064 R6556 G1 225.01 N 6 43081542 C112Y C T missense Het probably damaging 0.999 06/06/2018
20 522164 UTSW Gtf2h1 0.971 R6556 G1 225.01 N 7 46808665 C245S T A missense Het probably damaging 1.000 06/06/2018
21 522158 UTSW Hdhd5 0.103 R6556 G1 225.01 N 6 120523554 H61R T C missense Het probably benign 0.001 06/06/2018
22 522197 UTSW Ighv1-71 R6556 G1 139.01 N 12 115742472 V31E A T missense Het probably damaging 0.990 06/06/2018
23 522174 UTSW Igsf9b 0.607 R6556 G1 225.01 N 9 27329555 F688S T C missense Het probably damaging 1.000 06/06/2018
24 522152 UTSW Iqcd 0.073 R6556 G1 225.01 N 5 120602378 V258A T C missense Het probably damaging 0.987 06/06/2018
25 522183 UTSW Kcnc2 0.000 R6556 G1 198.01 N 10 112271856 G51R G C missense Het probably benign 0.037 0.103 phenotype 06/06/2018
26 522189 UTSW Lpo 0.000 R6556 G1 225.01 N 11 87817763 Y136* G T nonsense Het probably null phenotype 06/06/2018
27 522203 UTSW Med30 R6556 G1 86.01 N 15 52730383 A G utr 3 prime Het probably benign phenotype 06/06/2018
28 522140 UTSW Mertk 0.189 R6556 G1 225.01 N 2 128776421 V524D T A missense Het probably benign 0.229 phenotype 06/06/2018
29 522134 UTSW Olfr1156 0.090 R6556 G1 225.01 N 2 87949976 I86V T C missense Het probably benign 0.005 phenotype 06/06/2018
30 522136 UTSW Olfr1261 0.052 R6556 G1 225.01 N 2 89994173 F260Y T A missense Het probably benign 0.394 phenotype 06/06/2018
31 522138 UTSW Olfr1263 0.097 R6556 G1 225.01 N 2 90015094 Y55H T C missense Het probably damaging 1.000 phenotype 06/06/2018
32 522149 UTSW Pde6b 0.000 R6556 G1 225.01 N 5 108421501 M358K T A missense Het possibly damaging 0.564 phenotype 06/06/2018
33 522179 UTSW Prep 1.000 R6556 G1 217.47 N 10 45158314 GA G frame shift Het probably null phenotype 06/06/2018
34 522199 UTSW Prpf4b 1.000 R6556 G1 225.01 N 13 34896032 R793Q G A missense Het probably damaging 0.983 phenotype 06/06/2018
35 522216 UTSW Rela 1.000 R6556 G1 225.01 N 19 5647338 N524K T A missense Het probably damaging 1.000 phenotype 06/06/2018
36 522207 UTSW Rnaset2a 0.310 R6556 G1 145.01 N 17 8141648 D74G T C missense Het probably damaging 0.999 06/06/2018
37 522146 UTSW Serinc2 0.095 R6556 G1 225.01 N 4 130258271 I267F T A missense Het probably damaging 0.999 06/06/2018
38 522172 UTSW Sesn3 0.000 R6556 G1 225.01 N 9 14321253 F274S T C missense Het possibly damaging 0.950 phenotype 06/06/2018
39 522202 UTSW Spag1 0.793 R6556 G1 225.01 N 15 36195407 Y249H T C missense Het probably damaging 1.000 phenotype 06/06/2018
40 522195 UTSW Sstr1 1.000 R6556 G1 225.01 N 12 58213692 D367V A T missense Het possibly damaging 0.936 phenotype 06/06/2018
41 522162 UTSW Tnnt1 0.140 R6556 G1 225.01 N 7 4509577 E110G T C missense Het probably damaging 0.999 phenotype 06/06/2018
42 522177 UTSW Tpm1 1.000 R6556 G1 225.01 N 9 67028169 T A critical splice acceptor site Het probably null phenotype 06/06/2018
43 522214 UTSW Unc93b1 0.000 R6556 G1 225.01 N 19 3944105 V412A T C missense Het probably benign 0.000 phenotype 06/06/2018
44 522142 UTSW Uox 0.454 R6556 G1 225.01 N 3 146624648 G C critical splice donor site 1 bp Het probably null phenotype 06/06/2018
45 522181 UTSW Usp44 0.000 R6556 G1 225.01 N 10 93846008 Y107H T C missense Het probably benign 0.196 phenotype 06/06/2018
[records 1 to 45 of 45]