Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
4 are Possibly Damaging.
9 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 26 of 26] 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 156124 UTSW 4931440F15Rik 0.098 R1329 G1 225 N 11 29823553 N635Y T A missense Het probably benign 0.007 02/11/2014
2 156110 UTSW Acot7 0.177 R1329 G1 225 N 4 152229784 Q188* C T nonsense Het probably null phenotype 02/11/2014
3 156114 UTSW Ano5 0.102 R1329 G1 225 N 7 51546785 Y141H T C missense Het probably benign 0.000 phenotype 02/11/2014
4 156126 UTSW Atg101 0.276 R1329 G1 225 N 15 101290290 G92D G A missense Het probably null 0.483 02/11/2014
5 156127 UTSW Brwd1 0.000 R1329 G1 225 N 16 96003234 I1912T A G missense Het probably benign 0.066 phenotype 02/11/2014
6 156112 UTSW C530008M17Rik 0.000 R1329 G1 198 N 5 76657932 A G intron Het probably benign 02/11/2014
7 156111 UTSW Cad 0.967 R1329 G1 225 N 5 31059582 G263W G T missense Het probably damaging 1.000 phenotype 02/11/2014
8 156120 UTSW Clstn2 0.000 R1329 G1 203 N 9 97458174 E715G T C missense Het probably damaging 1.000 phenotype 02/11/2014
9 156113 UTSW Dbp 0.405 R1329 G1 225 N 7 45708328 P70S C T missense Het probably damaging 0.998 phenotype 02/11/2014
10 156108 UTSW Gpr61 0.000 R1329 G1 225 N 3 108150514 H277L T A missense Het probably benign 0.155 phenotype 02/11/2014
11 156125 UTSW Gsdma3 0.094 R1329 G1 225 N 11 98632392 V203F G T missense Het probably damaging 0.996 phenotype 02/11/2014
12 156106 UTSW Ifih1 0.150 R1329 G1 225 N 2 62617487 G C splice site Het probably null phenotype 02/11/2014
13 156119 UTSW Myo1e 0.000 R1329 G1 225 N 9 70338738 C404S T A missense Het possibly damaging 0.956 phenotype 02/11/2014
14 156123 UTSW Myrfl 0.000 R1329 G1 225 N 10 116777342 A G critical splice donor site 2 bp Het probably null 0.949 02/11/2014
15 156116 UTSW Nfat5 0.882 R1329 G1 225 N 8 107369027 M1300R T G missense Het probably benign 0.417 phenotype 02/11/2014
16 156117 UTSW Nfrkb 0.712 R1329 G1 225 N 9 31414647 P1129S C T missense Het possibly damaging 0.930 02/11/2014
17 156129 UTSW Nubp2 1.000 R1329 G1 176 N 17 24883864 N208K A T missense Het possibly damaging 0.906 phenotype 02/11/2014
18 156118 UTSW Olfr44 0.067 R1329 G1 225 N 9 39484444 S270P A G missense Het probably damaging 0.970 phenotype 02/11/2014
19 156115 UTSW Ovch2 0.000 R1329 G1 225 N 7 107785446 D488G T C missense Het probably damaging 1.000 02/11/2014
20 156122 UTSW Rfx6 1.000 R1329 G1 225 N 10 51693737 Y202F A T missense Het probably damaging 1.000 phenotype 02/11/2014
21 156107 UTSW Rin2 0.180 R1329 G1 225 N 2 145860446 T354I C T missense Het probably benign 0.005 0.063 phenotype 02/11/2014
22 156121 UTSW Usp4 0.150 R1329 G1 225 N 9 108372566 V431E T A missense Het probably damaging 0.996 phenotype 02/11/2014
23 156103 UTSW Vil1 0.325 R1329 G1 215 N 1 74427558 I636V A G missense Het probably benign 0.001 phenotype 02/11/2014
24 156128 UTSW Vmn2r116 0.078 R1329 G1 225 N 17 23387188 N358S A G missense Het possibly damaging 0.893 phenotype 02/11/2014
25 156109 UTSW Wdr47 0.000 R1329 G1 225 N 3 108627299 N511K T A missense Het probably benign 0.143 02/11/2014
26 156104 UTSW Wdr5 0.963 R1329 G1 225 N 2 27531671 F222I T A missense Het probably damaging 1.000 phenotype 02/11/2014
[records 1 to 26 of 26]