Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
4 are Possibly Damaging.
10 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 269901 UTSW Afap1l2 0.090 R3698 G1 225 N 19 56916523 S549I C A missense Het possibly damaging 0.691 03/18/2015
2 269884 UTSW Aldh4a1 0.083 R3698 G1 225 N 4 139642251 H371R A G missense Het possibly damaging 0.683 0.091 phenotype 03/18/2015
3 269886 UTSW Arpc1a 0.844 R3698 G1 225 N 5 145096191 K103N G T missense Het probably damaging 0.981 phenotype 03/18/2015
4 269899 UTSW Btg3 0.144 R3698 G1 204 N 16 78364834 S136P A G missense Het probably benign 0.000 phenotype 03/18/2015
5 269879 UTSW Ckap5 1.000 R3698 G1 225 N 2 91620166 T2014K C A missense Het probably benign 0.154 0.116 phenotype 03/18/2015
6 269883 UTSW Emc1 0.963 R3698 G1 225 N 4 139365386 S546A T G missense Het possibly damaging 0.460 0.074 phenotype 03/18/2015
7 269902 UTSW Fam45a 0.075 R3698 G1 199 N 19 60832616 A G unclassified 1752 bp Het probably null 03/18/2015
8 269885 UTSW G3bp2 1.000 R3698 G1 225 N 5 92056280 E316G T C missense Het possibly damaging 0.910 03/18/2015
9 269880 UTSW Il12a 0.000 R3698 G1 217 N 3 68697987 TCAC TC frame shift Het probably null 0.976 phenotype 03/18/2015
10 269897 UTSW Il6st 1.000 R3698 G1 225 N 13 112504382 D897E T G missense Het probably benign 0.129 0.064 phenotype 03/18/2015
11 269882 UTSW Ipo13 0.955 R3698 G1 225 N 4 117900693 L767P A G missense Het probably damaging 1.000 phenotype 03/18/2015
12 269881 UTSW Kcnd3 0.000 R3698 G1 187 N 3 105658766 A421V C T missense Het probably damaging 1.000 0.147 phenotype 03/18/2015
13 269903 UTSW Klhl13 0.111 R3698 G1 222 N X 23248183 T94I G A missense Het probably benign 0.063 phenotype 03/18/2015
14 269895 UTSW Morc2a 1.000 R3698 G1 225 N 11 3679672 K364* A T nonsense Het probably null phenotype 03/18/2015
15 269889 UTSW Nat8f2 0.000 R3698 G1 225 N 6 85867796 T195S T A missense Het probably benign 0.164 03/18/2015
16 269892 UTSW Nckipsd 0.374 R3698 G1 225 N 9 108811121 G83S G A missense Het probably damaging 1.000 phenotype 03/18/2015
17 269890 UTSW Nfu1 0.844 R3698 G1 225 N 6 87015652 T83A A G missense Het probably damaging 1.000 0.560 phenotype 03/18/2015
18 269896 UTSW Nid1 0.222 R3698 G1 225 N 13 13486759 C748Y G A missense Het probably damaging 0.992 0.974 phenotype 03/18/2015
19 269878 UTSW Olfr1138 0.078 R3698 G1 225 N 2 87738016 T103A T C missense Het probably benign 0.000 0.090 phenotype 03/18/2015
20 269875 UTSW Olfr366 0.102 R3698 G1 225 N 2 37220176 P229L C T missense Het probably damaging 0.975 0.562 phenotype 03/18/2015
21 269898 UTSW Rgs22 0.000 R3698 G1 225 N 15 36099892 V226I C T missense Het probably benign 0.001 0.090 03/18/2015
22 269887 UTSW Slc13a4 0.856 R3698 G1 225 N 6 35274957 I467F T A missense Het probably benign 0.063 phenotype 03/18/2015
23 269894 UTSW Stat2 0.189 R3698 G1 225 N 10 128278793 L253Q T A missense Het probably benign 0.301 phenotype 03/18/2015
24 269900 UTSW Tnxb 0.000 R3698 G1 225 N 17 34690433 G T critical splice donor site 1 bp Het probably null phenotype 03/18/2015
25 269877 UTSW Ttn 1.000 R3698 G1 225 N 2 76734251 R28514H C T missense Het probably damaging 0.999 phenotype 03/18/2015
26 269893 UTSW Usp15 0.000 R3698 G1 225 N 10 123181738 D51G T C missense Het probably damaging 1.000 phenotype 03/18/2015
27 269891 UTSW Uvrag 0.961 R3698 G1 225 N 7 98939943 E417G T C missense Het probably damaging 0.999 phenotype 03/18/2015
[records 1 to 27 of 27]