Incidental Mutations

46 incidental mutations are currently displayed, and affect 44 genes.
5 are Possibly Damaging.
16 are Probably Damaging.
12 are Probably Benign.
11 are Probably Null.
4 create premature stop codons.
5 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46] 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 398067 UTSW 2700049A03Rik 1.000 R5190 G1 225 N 12 71164546 E685* G T nonsense Het probably null 0.976 phenotype 07/06/2016
2 398068 UTSW 2700049A03Rik 1.000 R5190 G1 225 N 12 71164547 E685V A T missense Het possibly damaging 0.931 0.181 phenotype 07/06/2016
3 398059 UTSW Abca7 0.000 R5190 G1 225 N 10 79999593 T C critical splice donor site 2 bp Het probably null phenotype 07/06/2016
4 398066 UTSW Abca8a 0.063 R5190 G1 225 N 11 110089909 C T critical splice donor site 1 bp Het probably null 07/06/2016
5 398077 UTSW Ablim3 0.113 R5190 G1 225 N 18 61819911 Y361H A G missense Het probably benign 0.002 phenotype 07/06/2016
6 398047 UTSW Acan 1.000 R5190 G1 225 N 7 79098541 T1020I C T missense Het probably benign 0.029 phenotype 07/06/2016
7 398037 UTSW Baat 0.000 R5190 G1 225 N 4 49499652 L218P A G missense Het probably damaging 1.000 phenotype 07/06/2016
8 398069 UTSW Bcl11b 1.000 R5190 G1 225 N 12 107989716 C58F C A missense Het probably damaging 0.998 phenotype 07/06/2016
9 398044 UTSW Cand2 0.000 R5190 G1 164 N 6 115789513 A360S G T missense Het probably damaging 0.999 07/06/2016
10 398075 UTSW Cdh2 1.000 R5190 G1 225 N 18 16650315 V62A A G missense Het possibly damaging 0.536 phenotype 07/06/2016
11 398052 UTSW Cep44 0.831 R5190 G1 225 N 8 56532796 V354I C T missense Het probably benign 0.053 07/06/2016
12 398029 UTSW Col3a1 0.849 R5190 G1 225 N 1 45329084 R309Q G A missense Het unknown phenotype 07/06/2016
13 398030 UTSW Col3a1 0.849 R5190 G1 225 N 1 45344807 G A intron Het probably benign phenotype 07/06/2016
14 398041 UTSW Coq5 0.966 R5190 G1 225 N 5 115295780 A G splice site 3 bp Het probably null 07/06/2016
15 398082 UTSW Crtac1 0.411 R5190 G1 225 N 19 42333908 I131T A G missense Het possibly damaging 0.496 phenotype 07/06/2016
16 398036 UTSW Decr1 0.740 R5190 G1 225 N 4 15924270 V217M C T missense Het probably damaging 1.000 phenotype 07/06/2016
17 478116 UTSW Dnajc13 0.947 R5190 G1 225 N 9 104174525 V1706A A G missense Het probably benign 0.001 phenotype 05/25/2017
18 398057 UTSW Dopey1 0.403 R5190 G1 225 N 9 86487304 I63M A G missense Het probably damaging 1.000 07/06/2016
19 398035 UTSW F830045P16Rik 0.058 R5190 G1 225 N 2 129472715 D214G T C missense Het probably benign 0.011 07/06/2016
20 398042 UTSW Fam216a 0.000 R5190 G1 225 N 5 122367521 T A critical splice acceptor site Het probably null 07/06/2016
21 398055 UTSW Fdxacb1 0.000 R5190 G1 225 N 9 50772087 H248P A C missense Het possibly damaging 0.779 phenotype 07/06/2016
22 398039 UTSW Gnai1 0.000 R5190 G1 225 N 5 18291598 V109E A T missense Het probably benign 0.000 phenotype 07/06/2016
23 478115 UTSW Helz2 0.000 R5190 G1 225 N 2 181230757 A T critical splice donor site 2 bp Het probably null phenotype 05/25/2017
24 398051 UTSW Itgam 0.107 R5190 G1 225 N 7 128116317 T C splice site 2 bp Het probably null phenotype 07/06/2016
25 398031 UTSW Kcnh1 0.174 R5190 G1 136 N 1 192505528 S766G A G missense Het probably benign 0.005 phenotype 07/06/2016
26 398045 UTSW Klra1 0.049 R5190 G1 225 N 6 130375278 C167F C A missense Het probably damaging 1.000 07/06/2016
27 398065 UTSW Krtap9-3 0.123 R5190 G1 225 N 11 99597982 T25S T A missense Het probably benign 0.000 phenotype 07/06/2016
28 398056 UTSW Mapk6 0.489 R5190 G1 114 N 9 75388344 Y624C T C missense Het probably damaging 0.995 phenotype 07/06/2016
29 398033 UTSW Olfr1123 0.386 R5190 G1 225 N 2 87418843 Y263C A G missense Het probably damaging 0.999 phenotype 07/06/2016
30 398034 UTSW Olfr1158 0.063 R5190 G1 225 N 2 87990763 Y217* T A nonsense Het probably null phenotype 07/06/2016
31 398061 UTSW Olfr1393 0.059 R5190 G1 225 N 11 49280382 V78A T C missense Het probably damaging 0.989 phenotype 07/06/2016
32 398063 UTSW Olfr51 0.055 R5190 G1 225 N 11 51007554 I194S T G missense Het probably damaging 0.984 phenotype 07/06/2016
33 398049 UTSW Olfr677 0.121 R5190 G1 225 N 7 105056453 S69L C T missense Het probably damaging 0.959 phenotype 07/06/2016
34 398073 UTSW P3h2 1.000 R5190 G1 225 N 16 25984949 S356P A G missense Het possibly damaging 0.861 phenotype 07/06/2016
35 398071 UTSW Pde12 1.000 R5190 G1 225 N 14 26666377 C T critical splice donor site 1 bp Het probably null 07/06/2016
36 398053 UTSW Rln3 R5190 G1 127 N 8 84043237 K94N T G missense Het probably damaging 0.997 phenotype 07/06/2016
37 398038 UTSW Skint5 0.057 R5190 G1 225 N 4 113763514 I668V T C missense Het unknown 07/06/2016
38 398072 UTSW Slitrk5 0.613 R5190 G1 225 N 14 111679420 Q159K C A missense Het probably damaging 0.999 phenotype 07/06/2016
39 398050 UTSW Trim3 0.000 R5190 G1 225 N 7 105619509 N79K G T missense Het probably damaging 1.000 phenotype 07/06/2016
40 398043 UTSW Tyw1 0.000 R5190 G1 225 N 5 130267915 C101* T A nonsense Het probably null phenotype 07/06/2016
41 398064 UTSW Ulk2 0.430 R5190 G1 225 N 11 61781711 T934A T C missense Het probably benign 0.000 phenotype 07/06/2016
42 398058 UTSW Unc5b 1.000 R5190 G1 225 N 10 60772293 Y687C T C missense Het probably benign 0.042 phenotype 07/06/2016
43 398070 UTSW Vmn1r195 0.050 R5190 G1 225 N 13 22278386 R9* C T nonsense Het probably null 07/06/2016
44 398060 UTSW Zfc3h1 0.941 R5190 G1 225 N 10 115418692 L1397R T G missense Het probably damaging 1.000 07/06/2016
45 398046 UTSW Zfp296 0.476 R5190 G1 175 N 7 19577407 V9A T C missense Het probably benign 0.326 07/06/2016
46 398054 UTSW Zfp423 0.877 R5190 G1 225 N 8 87782463 S397C T A missense Het probably damaging 1.000 phenotype 07/06/2016
[records 1 to 46 of 46]