Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
4 are Possibly Damaging.
8 are Probably Damaging.
10 are Probably Benign.
3 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 26 of 26] 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 328373 UTSW 4921536K21Rik 0.197 R4347 G1 225 Y 11 3890122 V92M C T missense Het probably damaging 0.988 0.068 07/07/2015
2 328378 UTSW 4930503E14Rik 0.059 R4347 G1 115 Y 14 44171178 R66S C A missense Het probably damaging 0.958 0.072 07/07/2015
3 328375 UTSW Abca5 0.159 R4347 G1 225 Y 11 110299968 I772N A T missense Het probably damaging 0.995 0.252 phenotype 07/07/2015
4 328376 UTSW Acox1 0.357 R4347 G1 225 Y 11 116198661 N15S T C missense Het probably benign 0.033 0.080 phenotype 07/07/2015
5 328381 UTSW Arhgap28 0.187 R4347 G1 225 Y 17 67873142 V233I C T missense Het probably benign 0.000 0.114 phenotype 07/07/2015
6 328361 UTSW Chil4 0.606 R4347 G1 203 Y 3 106202828 I317V T C missense Het probably benign 0.000 0.130 07/07/2015
7 328380 UTSW Dvl3 1.000 R4347 G1 225 Y 16 20531299 R645H G A missense Het possibly damaging 0.954 0.428 phenotype 07/07/2015
8 328368 UTSW Efl1 0.588 R4347 G1 225 Y 7 82697966 M567L A T missense Het probably damaging 0.999 0.364 phenotype 07/07/2015
9 328357 UTSW Gal3st2b 0.257 R4347 G1 225 Y 1 93939808 T59I C T missense Het probably damaging 1.000 0.029 07/07/2015
10 328358 UTSW Gm7135 0.338 R4347 G1 225 Y 1 97348310 T A exon Het noncoding transcript 0.044 07/07/2015
11 328379 UTSW Gpihbp1 0.000 R4347 G1 225 Y 15 75598168 *124G T G makesense Het probably null 0.649 phenotype 07/07/2015
12 328365 UTSW Igkv10-96 0.153 R4347 G1 225 Y 6 68632180 R44W T A missense Het probably benign 0.100 0.152 07/07/2015
13 328366 UTSW Igkv13-84 0.073 R4347 G1 225 Y 6 68939776 I19K T A missense Het probably benign 0.000 0.129 07/07/2015
14 328360 UTSW Kcnab1 0.106 R4347 G1 225 Y 3 65297475 A G intron Het probably benign 0.064 phenotype 07/07/2015
15 328363 UTSW Kif1b 1.000 R4347 G1 225 Y 4 149247234 G545C C A missense Het probably damaging 1.000 0.067 phenotype 07/07/2015
16 328374 UTSW Mprip 0.324 R4347 G1 225 Y 11 59759453 S1328P T C missense Het possibly damaging 0.864 0.071 07/07/2015
17 328372 UTSW Nrp1 1.000 R4347 G1 225 Y 8 128480991 T C critical splice donor site 2 bp Het probably null 0.506 phenotype 07/07/2015
18 328370 UTSW Olfml1 0.062 R4347 G1 225 Y 7 107567833 P23L C T missense Het probably benign 0.001 0.120 07/07/2015
19 328382 UTSW Plekhh2 0.162 R4347 G1 225 Y 17 84619702 A1457T G A missense Het probably benign 0.123 0.098 07/07/2015
20 328364 UTSW Prr27 0.004 R4347 G1 225 Y 5 87842672 I40V A G missense Het possibly damaging 0.455 0.212 07/07/2015
21 328362 UTSW Slc25a54 0.284 R4347 G1 225 Y 3 109102739 T185A A G missense Het possibly damaging 0.522 0.057 07/07/2015
22 328377 UTSW Srek1 0.800 R4347 G1 225 Y 13 103748759 G396D C T missense Het probably null 0.629 phenotype 07/07/2015
23 328383 UTSW Syvn1 1.000 R4347 G1 225 Y 19 6049921 C T intron Het probably benign 0.066 phenotype 07/07/2015
24 328369 UTSW Trim3 0.000 R4347 G1 225 Y 7 105619387 G120D C T missense Het probably damaging 1.000 0.084 phenotype 07/07/2015
25 328367 UTSW Usp5 1.000 R4347 G1 225 Y 6 124821195 Q409L T A missense Het probably damaging 0.995 0.234 phenotype 07/07/2015
26 328359 UTSW Vim 0.478 R4347 G1 225 Y 2 13575518 T G intron Het probably benign phenotype 07/07/2015
[records 1 to 26 of 26]