Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
6 are Possibly Damaging.
17 are Probably Damaging.
14 are Probably Benign.
5 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 42 of 42] 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 447547 UTSW 4930579F01Rik 0.049 R5812 G1 225 N 3 138176538 S9P A G missense Het probably damaging 0.999 12/15/2016
2 447585 UTSW Acsl5 0.000 R5812 G1 225 N 19 55294836 V615I G A missense Het probably benign 0.008 phenotype 12/15/2016
3 447560 UTSW Ankk1 0.054 R5812 G1 225 N 9 49426853 K47E T C missense Het probably benign 0.001 phenotype 12/15/2016
4 447558 UTSW Ankrd11 1.000 R5812 G1 225 N 8 122893805 A T splice site 3215 bp Het probably null phenotype 12/15/2016
5 447559 UTSW Bcl9l 0.000 R5812 G1 225 N 9 44506644 V593A T C missense Het probably benign 0.010 phenotype 12/15/2016
6 447573 UTSW Cadps 1.000 R5812 G1 225 N 14 12376685 I1271V T C missense Het probably benign 0.000 phenotype 12/15/2016
7 447572 UTSW Ccdc125 0.000 R5812 G1 225 N 13 100684304 W152R T C missense Het probably damaging 1.000 12/15/2016
8 447583 UTSW Cep192 0.000 R5812 G1 225 N 18 67851737 V1606A T C missense Het possibly damaging 0.492 12/15/2016
9 447557 UTSW Csgalnact1 0.074 R5812 G1 225 N 8 68401384 N255S T C missense Het probably benign 0.018 0.084 phenotype 12/15/2016
10 447581 UTSW Cxxc5 0.482 R5812 G1 171 N 18 35859056 V170E T A missense Het probably damaging 0.977 phenotype 12/15/2016
11 447556 UTSW Defb6 0.050 R5812 G1 225 N 8 19228094 R61C C T missense Het possibly damaging 0.842 12/15/2016
12 447552 UTSW Dnah10 0.000 R5812 G1 225 N 5 124747746 N655K T A missense Het probably benign 0.015 phenotype 12/15/2016
13 447553 UTSW Fry 0.709 R5812 G1 225 N 5 150399671 A1096T G A missense Het probably damaging 0.991 12/15/2016
14 447564 UTSW Gli1 0.000 R5812 G1 225 N 10 127337415 G125S C T missense Het probably damaging 1.000 phenotype 12/15/2016
15 447543 UTSW Gm5538 0.084 R5812 G1 225 N 3 59747272 Y176N T A missense Het probably damaging 1.000 12/15/2016
16 447554 UTSW Igkv14-126 0.424 R5812 G1 225 N 6 67896440 I51F A T missense Het possibly damaging 0.711 12/15/2016
17 447570 UTSW Itgb4 1.000 R5812 G1 225 N 11 115984157 R447W C T missense Het probably benign 0.002 0.090 phenotype 12/15/2016
18 447545 UTSW Jtb 1.000 R5812 G1 225 N 3 90233977 S87P T C missense Het probably benign 0.007 12/15/2016
19 447568 UTSW Kdm6b 1.000 R5812 G1 197 N 11 69405929 I504N A T missense Het probably damaging 0.982 phenotype 12/15/2016
20 447540 UTSW Lin9 1.000 R5812 G1 225 N 1 180669198 L351I T A missense Het probably benign 0.011 0.067 phenotype 12/15/2016
21 447567 UTSW Map2k4 1.000 R5812 G1 225 N 11 65735205 I136T A G missense Het probably damaging 1.000 phenotype 12/15/2016
22 447539 UTSW March4 0.163 R5812 G1 225 N 1 72428917 T319A T C missense Het probably benign 0.000 phenotype 12/15/2016
23 447561 UTSW Nr2e3 0.000 R5812 G1 217 N 9 59943418 TCCATCGGAGTGTTCCC TC small deletion Het probably benign phenotype 12/15/2016
24 447563 UTSW Nt5e 0.000 R5812 G1 225 N 9 88369055 V459A T C missense Het probably damaging 0.999 phenotype 12/15/2016
25 447574 UTSW Ogdhl 0.000 R5812 G1 225 N 14 32332865 K257E A G missense Het probably damaging 0.999 phenotype 12/15/2016
26 447569 UTSW Olfr1 0.148 R5812 G1 217 N 11 73395654 AGCGGTCGTAGGC AGC frame shift Het probably null 0.976 phenotype 12/15/2016
27 447578 UTSW Olfr117 0.058 R5812 G1 225 N 17 37659739 L198P A G missense Het probably damaging 1.000 phenotype 12/15/2016
28 447575 UTSW Osmr 0.057 R5812 G1 225 N 15 6837059 V378D A T missense Het probably damaging 0.994 phenotype 12/15/2016
29 447582 UTSW Pcdhb18 0.302 R5812 G1 225 N 18 37490484 R289Q G A missense Het probably benign 0.053 0.091 12/15/2016
30 447584 UTSW Pdzd7 0.254 R5812 G1 225 N 19 45036871 T395K G T missense Het probably damaging 1.000 phenotype 12/15/2016
31 447566 UTSW Rasgef1c 0.108 R5812 G1 209 N 11 49957143 D35G A G missense Het probably benign 0.010 12/15/2016
32 447550 UTSW Rbm19 1.000 R5812 G1 225 N 5 120141577 F770L T C missense Het probably damaging 0.999 phenotype 12/15/2016
33 447580 UTSW Rit2 0.071 R5812 G1 225 N 18 30975461 C157F C A missense Het probably damaging 0.995 phenotype 12/15/2016
34 462750 UTSW Slc22a22 0.056 R5812 G1 225 N 15 57256473 A G critical splice donor site 2 bp Het probably null 03/01/2017
35 447551 UTSW Slc8b1 0.000 R5812 G1 194 N 5 120513338 T C splice site 6 bp Het probably null phenotype 12/15/2016
36 447576 UTSW Speer2 0.071 R5812 G1 225 N 16 69858895 R14S C A missense Het possibly damaging 0.817 12/15/2016
37 447555 UTSW Tas2r105 0.046 R5812 G1 225 N 6 131686873 L197F C A missense Het possibly damaging 0.947 phenotype 12/15/2016
38 447549 UTSW Tmprss11b 0.000 R5812 G1 225 N 5 86665098 H113L T A missense Het possibly damaging 0.666 12/15/2016
39 447541 UTSW Ttbk2 1.000 R5812 G1 225 N 2 120822559 P64S G A missense Het probably damaging 0.991 phenotype 12/15/2016
40 447577 UTSW Urb1 1.000 R5812 G1 225 N 16 90804537 H115Q A T missense Het probably damaging 0.991 0.278 12/15/2016
41 447562 UTSW Vps13c 0.000 R5812 G1 225 N 9 67982495 T A splice site Het probably benign phenotype 12/15/2016
42 447565 UTSW Zbtb39 0.250 R5812 G1 225 N 10 127741560 M1K T A start codon destroyed Het probably null 0.988 12/15/2016
[records 1 to 42 of 42]