Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
6 are Possibly Damaging.
7 are Probably Damaging.
9 are Probably Benign.
3 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 25 of 25] 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 329799 UTSW Abcc8 0.525 R4444 G1 225 N 7 46136194 T695N G T missense Het probably benign 0.086 phenotype 07/21/2015
2 329795 UTSW Cdkl2 0.000 R4444 G1 225 N 5 92020309 T342I G A missense Het probably benign 0.097 0.059 phenotype 07/21/2015
3 329802 UTSW Cntn5 0.000 R4444 G1 225 N 9 9704942 E822D C A missense Het probably damaging 1.000 phenotype 07/21/2015
4 329813 UTSW Cysltr2 0.060 R4444 G1 225 N 14 73029893 H126Y G A missense Het possibly damaging 0.737 phenotype 07/21/2015
5 329800 UTSW Dlg2 0.000 R4444 G1 225 N 7 92088593 S428P T C missense Het probably damaging 1.000 phenotype 07/21/2015
6 329804 UTSW Egfr 0.924 R4444 G1 225 N 11 16871027 D314G A G missense Het probably benign 0.001 phenotype 07/21/2015
7 329790 UTSW Ercc5 1.000 R4444 G1 155 N 1 44158209 GAAAA GAAAAA frame shift Het probably null phenotype 07/21/2015
8 329807 UTSW Gemin4 0.961 R4444 G1 225 N 11 76212091 F615L A G missense Het probably benign 0.005 phenotype 07/21/2015
9 329798 UTSW Ggn 1.000 R4444 G1 225 N 7 29172160 T322A A G missense Het probably benign 0.063 phenotype 07/21/2015
10 329817 UTSW Hunk 0.000 R4444 G1 225 N 16 90432791 A180V C T missense Het probably benign 0.070 phenotype 07/21/2015
11 329816 UTSW Kalrn 0.925 R4444 G1 225 N 16 33989810 D2525N C T missense Het possibly damaging 0.722 0.091 phenotype 07/21/2015
12 329791 UTSW Myo1b 0.239 R4444 G1 225 N 1 51757919 I988N A T missense Het probably damaging 0.987 07/21/2015
13 329797 UTSW Nlrp4e 0.000 R4444 G1 225 N 7 23321227 I380V A G missense Het probably benign 0.006 07/21/2015
14 329801 UTSW Olfr694 0.113 R4444 G1 225 N 7 106689146 Y195F T A missense Het possibly damaging 0.599 phenotype 07/21/2015
15 500625 UTSW Plb1 0.055 R4444 G1 225 N 5 32330565 V930I G A missense Het probably benign 0.058 phenotype 12/01/2017
16 329792 UTSW Plxna2 0.000 R4444 G1 210 N 1 194749317 S538F C T missense Het probably damaging 0.999 0.769 phenotype 07/21/2015
17 329814 UTSW Retreg1 0.118 R4444 G1 225 N 15 25968444 T G unclassified 1752 bp Het probably null phenotype 07/21/2015
18 329794 UTSW Rnf13 0.000 R4444 G1 225 N 3 57820589 K230T A C missense Het probably damaging 1.000 0.152 phenotype 07/21/2015
19 329808 UTSW Rpl9-ps1 R4444 G1 225 N 11 83645381 I81V T C missense Het possibly damaging 0.566 07/21/2015
20 329796 UTSW Slco1c1 0.082 R4444 G1 225 N 6 141546691 T267A A G missense Het possibly damaging 0.956 phenotype 07/21/2015
21 329793 UTSW Spc25 0.960 R4444 G1 225 N 2 69204876 M47K A T missense Het probably benign 0.062 phenotype 07/21/2015
22 329809 UTSW Syne2 0.296 R4444 G1 225 N 12 76023030 E4377G A G missense Het probably damaging 0.998 phenotype 07/21/2015
23 329805 UTSW Usp34 0.300 R4444 G1 225 N 11 23435998 T2142A A G missense Het probably damaging 0.984 07/21/2015
24 329815 UTSW Zc3h7a 0.154 R4444 G1 225 N 16 11150593 A G critical splice donor site 2 bp Het probably null 07/21/2015
25 329810 UTSW Zfp169 0.066 R4444 G1 225 N 13 48490337 K438M T A missense Het possibly damaging 0.939 phenotype 07/21/2015
[records 1 to 25 of 25]