Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
5 are Possibly Damaging.
16 are Probably Damaging.
13 are Probably Benign.
8 are Probably Null.
3 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 43 of 43] 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 394423 UTSW 3632451O06Rik 0.000 R5047 G1 218 Y 14 49770438 A526D G T missense Het probably damaging 0.999 0.145 06/15/2016
2 394422 UTSW 4930503E14Rik 0.058 R5047 G1 183 N 14 44169241 M117K A T missense Het possibly damaging 0.871 06/15/2016
3 394401 UTSW Adamts13 0.088 R5047 G1 184 Y 2 26996910 A1020T G A missense Het probably damaging 0.984 0.647 phenotype 06/15/2016
4 453353 UTSW Atg3 1.000 R5047 G1 225 Y 16 45178232 D132E C A missense Het probably benign 0.001 0.169 phenotype 02/01/2017
5 453349 UTSW Blzf1 0.212 R5047 G1 52 Y 1 164306468 M4T A G missense Het possibly damaging 0.505 0.795 02/01/2017
6 394415 UTSW Cdon 0.356 R5047 G1 225 Y 9 35478639 R863Q G A missense Het probably damaging 1.000 0.254 phenotype 06/15/2016
7 394426 UTSW Cyp2d40 0.122 R5047 G1 225 Y 15 82760259 R255H C T missense Het unknown 0.096 06/15/2016
8 394409 UTSW Evi5 0.000 R5047 G1 225 Y 5 107821874 K57R T C missense Het probably damaging 1.000 0.147 06/15/2016
9 394427 UTSW Fam186b 0.000 R5047 G1 225 Y 15 99280686 E253G T C missense Het probably damaging 1.000 0.172 phenotype 06/15/2016
10 394405 UTSW Fcgr1 0.213 R5047 G1 225 Y 3 96285884 F266I A T missense Het probably benign 0.385 0.090 phenotype 06/15/2016
11 394437 UTSW Fchsd1 0.114 R5047 G1 95 Y 18 37959873 C T unclassified Het probably benign 0.090 06/15/2016
12 394418 UTSW Gm10142 0.071 R5047 G1 225 Y 10 77716162 C119F G T missense Het probably damaging 0.999 0.394 06/15/2016
13 394407 UTSW Gpr63 0.000 R5047 G1 225 Y 4 25008202 S309G A G missense Het probably benign 0.440 0.087 phenotype 06/15/2016
14 394410 UTSW Herc3 0.000 R5047 G1 225 Y 6 58855760 Q137* C T nonsense Het probably null 0.976 phenotype 06/15/2016
15 394421 UTSW Jmy 0.137 R5047 G1 225 Y 13 93441572 H696L T A missense Het possibly damaging 0.650 0.162 06/15/2016
16 394420 UTSW Kif13a 0.338 R5047 G1 165 Y 13 46788085 H972R T C missense Het probably benign 0.001 0.073 phenotype 06/15/2016
17 394434 UTSW Lama1 1.000 R5047 G1 225 Y 17 67743281 Q296* C T nonsense Het probably null 0.975 phenotype 06/15/2016
18 394432 UTSW Lmf1 1.000 R5047 G1 128 Y 17 25631838 C T intron Het probably benign phenotype 06/15/2016
19 394430 UTSW Lpp 0.158 R5047 G1 213 Y 16 24971846 C352R T C missense Het probably damaging 1.000 0.958 phenotype 06/15/2016
20 394435 UTSW Ltbp1 1.000 R5047 G1 185 Y 17 75292886 T C splice site Het probably benign phenotype 06/15/2016
21 394404 UTSW Maml3 0.000 R5047 G1 212 Y 3 51690841 D807E G T missense Het possibly damaging 0.882 0.179 phenotype 06/15/2016
22 394433 UTSW Mdc1 0.913 R5047 G1 225 Y 17 35847844 V372D T A missense Het probably benign 0.002 0.118 phenotype 06/15/2016
23 394417 UTSW Mst1 0.000 R5047 G1 225 Y 9 108084309 H579Q C A missense Het probably benign 0.174 0.090 phenotype 06/15/2016
24 394403 UTSW Olfr1238 0.117 R5047 G1 225 Y 2 89406713 V122A A G missense Het probably damaging 1.000 0.647 phenotype 06/15/2016
25 394416 UTSW Olfr26 0.067 R5047 G1 225 Y 9 38855289 V76I G A missense Het probably benign 0.358 0.209 phenotype 06/15/2016
26 394419 UTSW Olfr398 0.138 R5047 G1 223 Y 11 73984378 T77A T C missense Het probably damaging 1.000 0.293 phenotype 06/15/2016
27 394424 UTSW Olfr739 0.052 R5047 G1 225 Y 14 50425239 F240S T C missense Het probably damaging 0.997 0.159 phenotype 06/15/2016
28 394436 UTSW Pcdhb22 0.000 R5047 G1 225 Y 18 37519126 G216C G T missense Het probably damaging 1.000 0.852 phenotype 06/15/2016
29 394414 UTSW Phlpp2 0.171 R5047 G1 225 Y 8 109913619 H472L A T missense Het probably benign 0.041 0.133 phenotype 06/15/2016
30 453352 UTSW Plscr3 0.000 R5047 G1 64 Y 11 69850091 A G splice site 1716 bp Het probably null 0.824 phenotype 02/01/2017
31 394411 UTSW Rab7 0.840 R5047 G1 225 Y 6 88005223 A T splice site Het probably null 0.976 phenotype 06/15/2016
32 453351 UTSW Rad50 1.000 R5047 G1 206 Y 11 53674696 A G critical splice donor site 2 bp Het probably null phenotype 02/01/2017
33 394412 UTSW Scgb1b20 0.068 R5047 G1 225 Y 7 33373312 A G splice site Het probably null 0.976 06/15/2016
34 394402 UTSW Scn9a 1.000 R5047 G1 225 Y 2 66562480 L256R A C missense Het probably damaging 1.000 0.772 phenotype 06/15/2016
35 394425 UTSW Spag1 0.716 R5047 G1 225 Y 15 36195442 Q260H G T missense Het probably damaging 1.000 0.117 phenotype 06/15/2016
36 394400 UTSW Tatdn3 0.000 R5047 G1 225 Y 1 191046278 I239F T A missense Het probably damaging 1.000 0.842 06/15/2016
37 394438 UTSW Tcof1 1.000 R5047 G1 225 Y 18 60831914 S578P A G missense Het possibly damaging 0.856 0.179 phenotype 06/15/2016
38 394428 UTSW Top3b 0.300 R5047 G1 225 Y 16 16891418 T657A A G missense Het probably benign 0.001 0.082 phenotype 06/15/2016
39 453350 UTSW Tstd3 0.062 R5047 G1 225 Y 4 21759621 A G critical splice donor site 2 bp Het probably null 0.947 02/01/2017
40 394408 UTSW Ttc4 0.946 R5047 G1 200 Y 4 106668238 L233H A T missense Het probably damaging 1.000 0.145 phenotype 06/15/2016
41 394431 UTSW Vmn2r-ps130 0.131 R5047 G1 143 Y 17 23063820 M158K T A missense Het probably benign 0.000 0.090 06/15/2016
42 394429 UTSW Yeats2 0.956 R5047 G1 225 Y 16 20208465 Q822L A T missense Het probably damaging 1.000 0.138 phenotype 06/15/2016
43 394413 UTSW Zfp976 0.087 R5047 G1 225 Y 7 42613419 C331* A T nonsense Het probably null 0.976 06/15/2016
[records 1 to 43 of 43]