Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
7 are Possibly Damaging.
6 are Probably Damaging.
6 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 21 of 21] 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 156241 UTSW Atoh1 1.000 R1354 G1 182 N 6 64729357 E12G A G missense Het possibly damaging 0.528 phenotype 02/11/2014
2 156234 UTSW Ccdc183 0.084 R1354 G1 225 N 2 25612139 N241S T C missense Het probably benign 0.333 02/11/2014
3 156251 UTSW Cmya5 0.263 R1354 G1 225 N 13 93092058 T2174I G A missense Het possibly damaging 0.459 02/11/2014
4 156242 UTSW Edem1 0.245 R1354 G1 225 N 6 108854316 I579M A G missense Het possibly damaging 0.929 02/11/2014
5 156240 UTSW Gimap9 0.056 R1354 G1 225 N 6 48678048 M190L A T missense Het probably benign 0.239 phenotype 02/11/2014
6 156247 UTSW Glod4 0.145 R1354 G1 225 N 11 76237828 A T splice site Het probably null 02/11/2014
7 262755 UTSW Ighv8-6 R1354 G1 225 N 12 115166080 S19T A T missense Het probably damaging 0.987 02/04/2015
8 156238 UTSW Lef1 1.000 R1354 G1 225 N 3 131194668 P267S C T missense Het probably damaging 1.000 phenotype 02/11/2014
9 156245 UTSW Megf11 0.306 R1354 G1 110 N 9 64653177 E335G A G missense Het probably benign 0.001 phenotype 02/11/2014
10 156243 UTSW Muc5ac 0.000 R1354 G1 225 N 7 141807377 N1475S A G missense Het probably damaging 0.994 phenotype 02/11/2014
11 156252 UTSW Ndst2 0.370 R1354 G1 225 N 14 20724975 R749L C A missense Het possibly damaging 0.741 phenotype 02/11/2014
12 156239 UTSW Oas3 0.072 R1354 G1 225 N 5 120770000 V292L C A missense Het possibly damaging 0.942 phenotype 02/11/2014
13 156249 UTSW Phactr1 0.000 R1354 G1 218 N 13 43057331 I210F A T missense Het possibly damaging 0.912 phenotype 02/11/2014
14 156237 UTSW Plppr5 0.080 R1354 G1 225 N 3 117575847 R51H G A missense Het possibly damaging 0.942 phenotype 02/11/2014
15 156233 UTSW Ppp1r12b 0.264 R1354 G1 225 N 1 134835983 T771M G A missense Het probably benign 0.417 02/11/2014
16 156250 UTSW Rasgrf2 0.256 R1354 G1 225 N 13 92028666 P331S G A missense Het probably damaging 1.000 phenotype 02/11/2014
17 156254 UTSW Rtl6 0.088 R1354 G1 225 N 15 84556527 V223M C T missense Het probably damaging 0.985 02/11/2014
18 156244 UTSW Tbc1d9 0.371 R1354 G1 225 N 8 83268981 A C critical splice acceptor site Het probably null 02/11/2014
19 156235 UTSW Tgm3 0.000 R1354 G1 225 N 2 130041898 I492T T C missense Het probably benign 0.000 phenotype 02/11/2014
20 226094 UTSW Trdv1 0.040 R1354 G1 225 N 14 53881918 T A intron Het probably benign 09/11/2014
21 156248 UTSW Wdr45b 0.183 R1354 G1 225 N 11 121335430 I191N A T missense Het probably damaging 0.982 phenotype 02/11/2014
[records 1 to 21 of 21]