Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
7 are Possibly Damaging.
10 are Probably Damaging.
8 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 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 76961 UTSW Abr 0.585 R0771 G1 225 N 11 76455683 E434G T C missense Het probably damaging 1.000 phenotype 10/16/2013
2 76960 UTSW Adam19 1.000 R0771 G1 225 N 11 46121453 V259I G A missense Het possibly damaging 0.915 phenotype 10/16/2013
3 76954 UTSW Adam5 0.058 R0771 G1 225 N 8 24786299 S451P A G missense Het probably benign 0.039 phenotype 10/16/2013
4 76944 UTSW Chd6 0.849 R0771 G1 225 N 2 161019580 L516F G A missense Het probably damaging 1.000 phenotype 10/16/2013
5 76955 UTSW Elovl4 1.000 R0771 G1 225 N 9 83785115 V154A A G missense Het possibly damaging 0.948 phenotype 10/16/2013
6 76956 UTSW Gadl1 0.114 R0771 G1 225 N 9 115944232 R114Q G A missense Het probably damaging 0.998 10/16/2013
7 76950 UTSW Gm5065 0.646 R0771 G1 225 N 7 5359823 D151G A G missense Het probably damaging 0.997 10/16/2013
8 76945 UTSW Gm9733 0.061 R0771 G1 225 N 3 15320446 Q132L T A missense Het probably benign 0.329 10/16/2013
9 76946 UTSW Ipo13 0.960 R0771 G1 225 N 4 117894646 N936S T C missense Het possibly damaging 0.783 phenotype 10/16/2013
10 76948 UTSW Kcnd2 0.145 R0771 G1 225 N 6 21216442 S48R T A missense Het probably damaging 1.000 phenotype 10/16/2013
11 76952 UTSW Lim2 0.169 R0771 G1 225 N 7 43430703 A38E C A missense Het possibly damaging 0.468 phenotype 10/16/2013
12 76942 UTSW Lrp2 1.000 R0771 G1 225 N 2 69507990 D1177E A T missense Het probably damaging 1.000 phenotype 10/16/2013
13 76959 UTSW Mdh1 1.000 R0771 G1 225 N 11 21557550 V300I C T missense Het probably benign 0.274 phenotype 10/16/2013
14 76957 UTSW Mfsd4b4 0.092 R0771 G1 222 N 10 39892411 T275A T C missense Het probably benign 0.011 10/16/2013
15 76966 UTSW Myo10 0.000 R0771 G1 225 N 15 25778178 Y114C A G missense Het probably damaging 1.000 phenotype 10/16/2013
16 76963 UTSW Ncapg2 1.000 R0771 G1 225 N 12 116413159 C122* T A nonsense Het probably null phenotype 10/16/2013
17 76949 UTSW Nod1 0.000 R0771 G1 225 N 6 54944269 S355R T G missense Het probably damaging 0.960 phenotype 10/16/2013
18 76943 UTSW Olfr1020 0.153 R0771 G1 225 N 2 85849994 I181F A T missense Het possibly damaging 0.952 phenotype 10/16/2013
19 76953 UTSW Olfr686 0.074 R0771 G1 225 N 7 105204161 M61L T A missense Het possibly damaging 0.912 phenotype 10/16/2013
20 76965 UTSW Pcsk1 1.000 R0771 G1 225 N 13 75132162 E702V A T missense Het probably benign 0.315 phenotype 10/16/2013
21 76962 UTSW Ptpn21 0.141 R0771 G1 225 N 12 98689080 T543A T C missense Het probably damaging 0.998 phenotype 10/16/2013
22 76964 UTSW Ranbp9 0.957 R0771 G1 225 N 13 43461773 I190V T C missense Het possibly damaging 0.915 phenotype 10/16/2013
23 76958 UTSW Slc1a4 0.000 R0771 G1 225 N 11 20306467 V455M C T missense Het probably damaging 1.000 phenotype 10/16/2013
24 76968 UTSW Srbd1 0.957 R0771 G1 225 N 17 86130254 E220D T A missense Het probably benign 0.091 10/16/2013
25 76947 UTSW Thsd7a 0.000 R0771 G1 225 N 6 12327577 V1432A A G missense Het probably benign 0.092 phenotype 10/16/2013
26 76951 UTSW Zfp61 0.061 R0771 G1 225 N 7 24293354 R71G T C missense Het probably benign 0.001 10/16/2013
[records 1 to 26 of 26]