Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
4 are Possibly Damaging.
22 are Probably Damaging.
10 are Probably Benign.
2 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 39 of 39] 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 485139 UTSW Ahnak 0.266 R6116 G1 225.01 N 19 9012963 T A intron Het probably benign phenotype 08/16/2017
2 485138 UTSW Apc 0.985 R6116 G1 225.01 N 18 34316455 I2101F A T missense Het probably damaging 0.999 phenotype 08/16/2017
3 485106 UTSW Bpifa3 0.027 R6116 G1 225.01 N 2 154133713 V68I G A missense Het possibly damaging 0.896 08/16/2017
4 485120 UTSW Csmd1 0.291 R6116 G1 225.01 N 8 16211850 I878F T A missense Het probably damaging 0.999 phenotype 08/16/2017
5 485141 UTSW Cyp2c67 0.051 R6116 G1 225.01 N 19 39617435 M339K A T missense Het probably damaging 0.998 08/16/2017
6 485124 UTSW Dock3 0.483 R6116 G1 225.01 N 9 106931962 Y1321H A G missense Het probably damaging 1.000 phenotype 08/16/2017
7 485137 UTSW Dsc1 0.121 R6116 G1 225.01 N 18 20097299 D316E G T missense Het probably benign 0.101 phenotype 08/16/2017
8 485130 UTSW Eno3 0.564 R6116 G1 190.01 N 11 70661575 T351M C T missense Het possibly damaging 0.698 phenotype 08/16/2017
9 485131 UTSW Erbb2 1.000 R6116 G1 225.01 N 11 98427399 F487Y T A missense Het probably damaging 0.998 phenotype 08/16/2017
10 485110 UTSW Exosc10 0.952 R6116 G1 225.01 N 4 148573353 L652P T C missense Het probably benign 0.078 phenotype 08/16/2017
11 485111 UTSW Glmn 1.000 R6116 G1 225.01 N 5 107557340 M470K A T missense Het probably damaging 1.000 phenotype 08/16/2017
12 485112 UTSW Gm15446 0.033 R6116 G1 225.01 N 5 109943036 C385S T A missense Het probably damaging 1.000 08/16/2017
13 485104 UTSW Gm597 0.015 R6116 G1 225.01 N 1 28778699 A84V G A missense Het probably benign 0.009 08/16/2017
14 485123 UTSW Hspa8 0.970 R6116 G1 191.01 N 9 40804975 E581G A G missense Het probably damaging 0.983 phenotype 08/16/2017
15 485105 UTSW Igfn1 0.187 R6116 G1 225.01 N 1 135970467 D787G T C missense Het probably benign 0.005 08/16/2017
16 485115 UTSW Igkv12-44 0.384 R6116 G1 225.01 N 6 69814854 T42A T C missense Het possibly damaging 0.482 08/16/2017
17 485133 UTSW Itsn2 0.000 R6116 G1 225.01 N 12 4629939 T C unclassified Het probably benign phenotype 08/16/2017
18 485128 UTSW Jade2 0.526 R6116 G1 225.01 N 11 51835633 E84G T C missense Het probably damaging 0.993 08/16/2017
19 485109 UTSW Lpar3 0.000 R6116 G1 225.01 N 3 146240597 M10K T A missense Het possibly damaging 0.703 phenotype 08/16/2017
20 485136 UTSW Lpin2 0.465 R6116 G1 216.01 N 17 71243930 D695G A G missense Het probably damaging 1.000 phenotype 08/16/2017
21 485119 UTSW Mosmo 0.216 R6116 G1 225.01 N 7 120726195 L7H T A missense Het probably damaging 1.000 08/16/2017
22 485140 UTSW Ms4a8a 0.055 R6116 G1 225.01 N 19 11081072 A9T C T missense Het unknown phenotype 08/16/2017
23 485125 UTSW Myb 1.000 R6116 G1 225.01 N 10 21154754 D48G T C missense Het probably damaging 1.000 phenotype 08/16/2017
24 485114 UTSW Neurod6 0.000 R6116 G1 225.01 N 6 55678791 Y287C T C missense Het probably damaging 0.999 phenotype 08/16/2017
25 485122 UTSW Olfr878 0.118 R6116 G1 225.01 N 9 37918659 M1V A G start codon destroyed Het probably null 0.936 phenotype 08/16/2017
26 485135 UTSW Olfr96 0.060 R6116 G1 225.01 N 17 37225568 T148A A G missense Het probably benign 0.001 phenotype 08/16/2017
27 485116 UTSW Olr1 0.000 R6116 G1 225.01 N 6 129499984 D106V T A missense Het probably damaging 0.996 phenotype 08/16/2017
28 485113 UTSW Peg10 1.000 R6116 G1 163.47 N 6 4756351 C CCCATCAGGA small insertion Het probably benign phenotype 08/16/2017
29 485108 UTSW Plch1 0.192 R6116 G1 225.01 N 3 63702023 R912H C T missense Het probably damaging 1.000 phenotype 08/16/2017
30 485118 UTSW Ppfia3 0.219 R6116 G1 225.01 N 7 45354703 Y505C T C missense Het probably damaging 1.000 phenotype 08/16/2017
31 485132 UTSW Sdk2 0.165 R6116 G1 225.01 N 11 113854364 I702F T A missense Het probably damaging 0.989 phenotype 08/16/2017
32 485129 UTSW Slc16a11 0.000 R6116 G1 225.01 N 11 70215436 F119L T C missense Het probably benign 0.080 08/16/2017
33 485107 UTSW Slc2a10 0.116 R6116 G1 220.01 N 2 165517703 T496P A C missense Het probably damaging 1.000 phenotype 08/16/2017
34 485121 UTSW Slc7a2 0.201 R6116 G1 225.01 N 8 40900169 Y181H T C missense Het probably damaging 0.977 phenotype 08/16/2017
35 485127 UTSW Stab2 0.000 R6116 G1 225.01 N 10 86907190 P1185Q G T missense Het probably damaging 1.000 phenotype 08/16/2017
36 485142 UTSW Tcf7l2 1.000 R6116 G1 225.01 N 19 55919014 S335R T A missense Het probably damaging 1.000 phenotype 08/16/2017
37 485126 UTSW Ttc41 0.304 R6116 G1 225.01 N 10 86759088 G A critical splice acceptor site Het probably null 08/16/2017
38 485117 UTSW Vmn2r32 0.077 R6116 G1 225.01 N 7 7464093 I812N A T missense Het probably damaging 1.000 08/16/2017
39 485134 UTSW Wdr24 0.912 R6116 G1 225.01 N 17 25824605 H134Y C T missense Het probably benign 0.000 08/16/2017
[records 1 to 39 of 39]