Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
7 are Possibly Damaging.
13 are Probably Damaging.
14 are Probably Benign.
9 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44] 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 430373 UTSW A930009A15Rik 0.105 R5486 G1 225 N 10 115579905 G T intron Het probably benign 10/05/2016
2 430370 UTSW Acad8 0.087 R5486 G1 99 N 9 26999495 M1K A T start codon destroyed Het probably null phenotype 10/05/2016
3 430367 UTSW Adam12 0.366 R5486 G1 212 N 7 133907672 R786S C A missense Het possibly damaging 0.752 phenotype 10/05/2016
4 430392 UTSW Add3 0.000 R5486 G1 225 N 19 53244387 V604I G A missense Het probably benign 0.001 phenotype 10/05/2016
5 430390 UTSW Alpk2 0.000 R5486 G1 155 N 18 65294354 A T splice site Het probably null 10/05/2016
6 430354 UTSW Ano3 0.087 R5486 G1 225 N 2 110745870 D102G T C missense Het probably damaging 0.996 phenotype 10/05/2016
7 430379 UTSW Bdp1 1.000 R5486 G1 225 N 13 100098510 Y192C T C missense Het probably damaging 1.000 phenotype 10/05/2016
8 430358 UTSW Bod1l 0.951 R5486 G1 225 N 5 41807181 D2693E A T missense Het possibly damaging 0.565 10/05/2016
9 430368 UTSW Ccdc7a 0.058 R5486 G1 225 N 8 128985403 N284D T C missense Het probably damaging 0.983 10/05/2016
10 430388 UTSW Clic6 0.217 R5486 G1 225 N 16 92529852 A G intron Het probably null phenotype 10/05/2016
11 430382 UTSW Cln5 0.254 R5486 G1 225 N 14 103076194 I294T T C missense Het probably damaging 0.981 phenotype 10/05/2016
12 501055 UTSW Cmklr1 0.218 R5486 G1 225 N 5 113614929 D4H C G missense Het possibly damaging 0.646 0.179 phenotype 12/01/2017
13 430385 UTSW Cyp2d9 0.062 R5486 G1 204 N 15 82452578 W43R T A missense Het probably damaging 0.959 10/05/2016
14 430372 UTSW Dnajb12 0.087 R5486 G1 217 N 10 59892752 GC G frame shift Het probably null 0.976 phenotype 10/05/2016
15 430374 UTSW Erlec1 0.000 R5486 G1 225 N 11 30935047 H413Q A T missense Het probably damaging 0.975 phenotype 10/05/2016
16 430363 UTSW Fam168a 0.172 R5486 G1 166 N 7 100834169 M203K T A missense Het probably damaging 0.987 10/05/2016
17 430375 UTSW Fat2 0.000 R5486 G1 225 N 11 55253681 S4122R A T missense Het probably benign 0.005 phenotype 10/05/2016
18 430387 UTSW Fgd4 0.000 R5486 G1 225 N 16 16475037 L272Q A T missense Het probably damaging 1.000 phenotype 10/05/2016
19 430357 UTSW Hpcal4 0.000 R5486 G1 225 N 4 123190764 K162R A G missense Het probably benign 0.000 phenotype 10/05/2016
20 430378 UTSW Iars 1.000 R5486 G1 225 N 13 49709573 T A splice site Het probably null phenotype 10/05/2016
21 430351 UTSW Lbr 0.839 R5486 G1 225 N 1 181818838 A G critical splice donor site 2 bp Het probably null phenotype 10/05/2016
22 430353 UTSW Lrp2 1.000 R5486 G1 225 N 2 69437465 I4259V T C missense Het probably benign 0.040 phenotype 10/05/2016
23 430348 UTSW Mcm3 1.000 R5486 G1 225 N 1 20814894 G189S C T missense Het probably damaging 1.000 phenotype 10/05/2016
24 430380 UTSW Nr1d2 0.000 R5486 G1 203 N 14 18206860 V137A A G missense Het possibly damaging 0.648 phenotype 10/05/2016
25 430365 UTSW Olfr646 0.254 R5486 G1 225 N 7 104106498 T73N C A missense Het probably damaging 0.991 phenotype 10/05/2016
26 430366 UTSW Olfr665 0.080 R5486 G1 225 N 7 104880961 C85S T A missense Het probably benign 0.017 phenotype 10/05/2016
27 430369 UTSW Olfr853 0.055 R5486 G1 225 N 9 19537294 V212A A G missense Het probably benign 0.000 phenotype 10/05/2016
28 430386 UTSW Pim3 0.000 R5486 G1 108 N 15 88863222 V97A T C missense Het possibly damaging 0.713 phenotype 10/05/2016
29 430381 UTSW Piwil2 0.000 R5486 G1 225 N 14 70401431 N479S T C missense Het probably benign 0.011 phenotype 10/05/2016
30 430361 UTSW Pld3 0.000 R5486 G1 178 N 7 27533731 W365L C A missense Het probably damaging 0.992 phenotype 10/05/2016
31 501054 UTSW Plk3 0.000 R5486 G1 225 N 4 117130403 E412* C A nonsense Het probably null phenotype 12/01/2017
32 430349 UTSW Psmd1 0.967 R5486 G1 167 N 1 86137050 I935V A G missense Het possibly damaging 0.588 phenotype 10/05/2016
33 430359 UTSW Sh2b2 0.943 R5486 G1 165 N 5 136232090 S91P A G missense Het probably benign 0.100 phenotype 10/05/2016
34 430391 UTSW Skor2 1.000 R5486 G1 225 N 18 76858700 N39S A G missense Het unknown phenotype 10/05/2016
35 430384 UTSW Slc22a22 0.087 R5486 G1 225 N 15 57263451 V55A A G missense Het probably damaging 0.974 10/05/2016
36 430350 UTSW Smg7 0.914 R5486 G1 225 N 1 152846176 S595P A G missense Het probably damaging 0.974 phenotype 10/05/2016
37 430355 UTSW Snrnp200 1.000 R5486 G1 225 N 2 127233066 P1520S C T missense Het possibly damaging 0.819 phenotype 10/05/2016
38 430371 UTSW Taar7a 0.094 R5486 G1 225 N 10 23992458 T342S T A missense Het probably benign 0.001 10/05/2016
39 430377 UTSW Tecpr2 0.000 R5486 G1 225 N 12 110933015 I606F A T missense Het probably benign 0.034 phenotype 10/05/2016
40 430376 UTSW Tex19.2 0.235 R5486 G1 225 N 11 121117478 M48K A T missense Het probably benign 0.161 Tex19.1 causes testis degeneration and male infertility owing to meiotic arrest in the germ cells. [provided by MGI curators] (source: MGI)">phenotype 10/05/2016
41 430389 UTSW Thoc1 1.000 R5486 G1 225 N 18 9992204 T511A A G missense Het probably benign 0.392 phenotype 10/05/2016
42 430364 UTSW Trpc2 0.000 R5486 G1 217 N 7 102095213 GTGTCCTA GTGTCCTATGTCCTA frame shift Het probably null phenotype 10/05/2016
43 430383 UTSW Ubr5 1.000 R5486 G1 225 N 15 38008739 A1077S C A missense Het probably benign 0.005 phenotype 10/05/2016
44 430360 UTSW Wdr95 0.095 R5486 G1 225 N 5 149596330 R571* A T nonsense Het probably null 10/05/2016
[records 1 to 44 of 44]