Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
6 are Possibly Damaging.
16 are Probably Damaging.
16 are Probably Benign.
5 are Probably Null.
1 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 542296 UTSW 2810474O19Rik 0.000 R6972 G1 225.01 Y 6 149326109 Y218N T A missense Het probably damaging 0.988 11/28/2018
2 542300 UTSW Abhd2 0.442 R6972 G1 225.01 Y 7 79354027 S285G A G missense Het probably benign 0.022 0.064 phenotype 11/28/2018
3 542307 UTSW Afg1l 0.088 R6972 G1 160.01 Y 10 42478374 T10A T C missense Het probably benign 0.004 phenotype 11/28/2018
4 542290 UTSW Akap9 0.490 R6972 G1 225.01 Y 5 4046699 N2525D A G missense Het possibly damaging 0.615 phenotype 11/28/2018
5 542277 UTSW B3gnt7 0.107 R6972 G1 225.01 Y 1 86305387 M1I G A start codon destroyed Het probably null 0.001 11/28/2018
6 542315 UTSW Bdp1 1.000 R6972 G1 225.01 Y 13 100037761 E2089G T C missense Het probably null 0.999 phenotype 11/28/2018
7 542281 UTSW Calcrl 1.000 R6972 G1 225.01 Y 2 84368578 I156L T G missense Het probably benign 0.000 phenotype 11/28/2018
8 542295 UTSW Cd69 0.074 R6972 G1 225.01 Y 6 129269580 S122G T C missense Het probably benign 0.001 0.090 phenotype 11/28/2018
9 542292 UTSW Chek2 0.000 R6972 G1 225.01 Y 5 110855839 T C splice site 6 bp Het probably null 0.976 phenotype 11/28/2018
10 542284 UTSW Ckap5 1.000 R6972 G1 225.01 Y 2 91606313 I1586K T A missense Het probably damaging 0.984 phenotype 11/28/2018
11 542316 UTSW Cyp4f14 0.000 R6972 G1 224.01 Y 17 32905509 A523T C T missense Het probably benign 0.003 0.090 phenotype 11/28/2018
12 542306 UTSW Dcaf1 1.000 R6972 G1 225.01 Y 9 106846772 C466* T A nonsense Het probably null 0.976 phenotype 11/28/2018
13 542314 UTSW Dcdc2a 0.266 R6972 G1 223.01 Y 13 25120389 A T intron Het probably benign phenotype 11/28/2018
14 542313 UTSW Eml5 0.275 R6972 G1 225.01 Y 12 98876180 I220V T C missense Het probably benign 0.001 0.074 11/28/2018
15 542298 UTSW Etv2 1.000 R6972 G1 225.01 Y 7 30634742 N189D T C missense Het probably benign 0.001 0.123 phenotype 11/28/2018
16 542310 UTSW Fam19a2 0.109 R6972 G1 225.01 Y 10 123704373 T45A A G missense Het probably benign 0.011 0.080 phenotype 11/28/2018
17 542299 UTSW Fuz 0.239 R6972 G1 225.01 Y 7 44897331 T C critical splice donor site Het probably benign 0.065 phenotype 11/28/2018
18 542312 UTSW Git1 1.000 R6972 G1 153.01 Y 11 77499521 V64G T G missense Het probably damaging 1.000 phenotype 11/28/2018
19 542297 UTSW Gm15922 0.058 R6972 G1 225.01 N 7 3737320 A301P C G missense Het probably damaging 0.999 11/28/2018
20 542294 UTSW Gpr162 0.097 R6972 G1 180.01 Y 6 124861309 R126H C T missense Het probably damaging 0.994 phenotype 11/28/2018
21 542302 UTSW Grm5 0.187 R6972 G1 225.01 Y 7 87602923 V127A T C missense Het probably benign 0.019 0.083 phenotype 11/28/2018
22 542293 UTSW Iqsec1 0.206 R6972 G1 225.01 Y 6 90676768 D665G T C missense Het probably damaging 1.000 phenotype 11/28/2018
23 542278 UTSW Kcnh1 0.149 R6972 G1 225.01 Y 1 192276836 I233V A G missense Het probably damaging 0.995 phenotype 11/28/2018
24 568326 UTSW Lmcd1 0.000 R6972 G1 78.01 Y 6 112310698 T115I C T missense Het probably damaging 1.000 phenotype 07/01/2019
25 542309 UTSW Mybpc1 0.782 R6972 G1 225.01 Y 10 88560361 E208G T C missense Het possibly damaging 0.500 phenotype 11/28/2018
26 542308 UTSW Nfic 0.368 R6972 G1 197.01 Y 10 81420357 A158S C A missense Het probably benign 0.002 phenotype 11/28/2018
27 542291 UTSW Nos3 0.000 R6972 G1 225.01 Y 5 24380243 I798L A T missense Het probably benign 0.000 phenotype 11/28/2018
28 542286 UTSW Ntrk1 1.000 R6972 G1 225.01 Y 3 87783981 L292Q A T missense Het probably damaging 1.000 0.736 phenotype 11/28/2018
29 542303 UTSW Olfr698 0.087 R6972 G1 225.01 Y 7 106752699 S230P A G missense Het possibly damaging 0.599 phenotype 11/28/2018
30 542280 UTSW Orc4 0.965 R6972 G1 225.01 Y 2 48927184 Q164R T C missense Het probably benign 0.025 0.090 phenotype 11/28/2018
31 542318 UTSW Pcdhb14 0.127 R6972 G1 225.01 Y 18 37449692 V617E T A missense Het probably damaging 0.999 11/28/2018
32 542311 UTSW Plscr3 0.000 R6972 G1 225.01 Y 11 69847958 E149K G A missense Het probably damaging 0.998 phenotype 11/28/2018
33 542285 UTSW Pltp 0.121 R6972 G1 225.01 Y 2 164846592 A G critical splice donor site 2 bp Het probably null 0.959 phenotype 11/28/2018
34 542289 UTSW Pramef6 0.052 R6972 G1 225.01 Y 4 143896902 L234P A G missense Het probably damaging 1.000 11/28/2018
35 542282 UTSW Prg2 0.000 R6972 G1 225.01 Y 2 84982273 R109H G A missense Het probably benign 0.138 phenotype 11/28/2018
36 542283 UTSW Ptprj 0.187 R6972 G1 111.04 N 2 90580403 S62F G A missense Het possibly damaging 0.914 phenotype 11/28/2018
37 542288 UTSW Skint3 0.063 R6972 G1 225.01 Y 4 112258892 S240T T A missense Het probably damaging 0.975 0.647 11/28/2018
38 542304 UTSW Smarca5 1.000 R6972 G1 225.01 Y 8 80704751 Y946H A G missense Het probably damaging 1.000 phenotype 11/28/2018
39 542317 UTSW Taf4b 0.465 R6972 G1 225.01 Y 18 14813347 V409A T C missense Het possibly damaging 0.858 phenotype 11/28/2018
40 542305 UTSW Trim29 0.000 R6972 G1 225.01 Y 9 43327112 N504K T A missense Het probably benign 0.008 phenotype 11/28/2018
41 542301 UTSW Vmn2r77 0.100 R6972 G1 225.01 Y 7 86802994 Y461H T C missense Het probably damaging 0.999 0.647 11/28/2018
42 542279 UTSW Zeb2 1.000 R6972 G1 225.01 Y 2 44997318 K531E T C missense Het probably damaging 0.999 0.437 phenotype 11/28/2018
43 542287 UTSW Zfp687 0.571 R6972 G1 225.01 Y 3 95009377 S813P A G missense Het possibly damaging 0.652 0.096 phenotype 11/28/2018
[records 1 to 43 of 43]