Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
7 are Possibly Damaging.
14 are Probably Damaging.
13 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 42 of 42] 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 437958 UTSW 5330417C22Rik 0.159 R5609 G1 225 N 3 108471415 I408F T A missense Het probably damaging 0.965 phenotype 10/26/2016
2 437979 UTSW Abca13 0.145 R5609 G1 225 N 11 9403874 I3732T T C missense Het probably benign 0.013 phenotype 10/26/2016
3 437959 UTSW Ago1 0.499 R5609 G1 225 N 4 126461037 K127N C A missense Het possibly damaging 0.798 phenotype 10/26/2016
4 437993 UTSW Akap8l 0.649 R5609 G1 225 N 17 32338400 N79S T C missense Het probably damaging 0.995 10/26/2016
5 437969 UTSW Ano5 0.151 R5609 G1 225 N 7 51593637 L836P T C missense Het probably damaging 0.999 phenotype 10/26/2016
6 457991 UTSW AY358078 0.128 R5609 G1 199 N 14 51804608 T147A A G missense Het unknown 02/16/2017
7 437965 UTSW BC049730 0.037 R5609 G1 225 N 7 24714286 R242S A T missense Het possibly damaging 0.533 10/26/2016
8 437996 UTSW Cabp4 0.000 R5609 G1 211 N 19 4139252 D102G T C missense Het probably benign 0.366 phenotype 10/26/2016
9 437976 UTSW Cdc34 0.292 R5609 G1 225 N 10 79684821 R61C C T missense Het probably damaging 0.972 phenotype 10/26/2016
10 437954 UTSW Chac1 0.182 R5609 G1 225 N 2 119351406 K2E A G missense Het unknown phenotype 10/26/2016
11 437982 UTSW Cltc 0.975 R5609 G1 225 N 11 86730267 V305I C T missense Het probably damaging 0.993 phenotype 10/26/2016
12 437971 UTSW Cog7 0.783 R5609 G1 206 N 7 121925460 T704A T C missense Het probably benign 0.116 phenotype 10/26/2016
13 437960 UTSW Cux1 0.860 R5609 G1 225 N 5 136392320 V184A A G missense Het probably damaging 0.995 phenotype 10/26/2016
14 437961 UTSW Daglb 0.167 R5609 G1 190 N 5 143478519 T262S A T missense Het probably benign 0.001 phenotype 10/26/2016
15 437985 UTSW Dglucy 0.121 R5609 G1 225 N 12 100787646 I12V A G missense Het probably null phenotype 10/26/2016
16 437951 UTSW Dnah7a 0.281 R5609 G1 225 N 1 53582594 V1124A A G missense Het probably benign 0.025 10/26/2016
17 437977 UTSW Eef2 0.982 R5609 G1 149 N 10 81178769 C CN frame shift Het probably null phenotype 10/26/2016
18 437966 UTSW Eif3k 0.903 R5609 G1 225 N 7 28981708 A9S C A missense Het probably benign 0.304 phenotype 10/26/2016
19 437987 UTSW Gli3 1.000 R5609 G1 225 N 13 15548453 M60L A T missense Het possibly damaging 0.823 phenotype 10/26/2016
20 437975 UTSW Hk1 0.317 R5609 G1 224 N 10 62342551 E4K C T missense Het probably benign 0.298 phenotype 10/26/2016
21 437967 UTSW Kmt2b 1.000 R5609 G1 225 N 7 30577145 V1701L C A missense Het probably damaging 0.987 phenotype 10/26/2016
22 437953 UTSW Lrp1b 0.000 R5609 G1 225 N 2 41341795 H1107R T C missense Het probably damaging 1.000 phenotype 10/26/2016
23 437980 UTSW Ncor1 1.000 R5609 G1 225 N 11 62358853 A G unclassified 2 bp Het probably null phenotype 10/26/2016
24 437991 UTSW Olfr191 0.085 R5609 G1 225 N 16 59086076 M136L T A missense Het possibly damaging 0.956 phenotype 10/26/2016
25 437978 UTSW Olfr814 0.057 R5609 G1 225 N 10 129874738 R6S T G missense Het probably benign 0.007 phenotype 10/26/2016
26 437972 UTSW Plekhg4 0.295 R5609 G1 225 N 8 105379502 G A critical splice donor site 1 bp Het probably null phenotype 10/26/2016
27 437973 UTSW Pmfbp1 0.144 R5609 G1 211 N 8 109525107 E327D G T missense Het probably damaging 1.000 10/26/2016
28 437990 UTSW Slc22a17 0.188 R5609 G1 161 N 14 54908970 P63L G A missense Het probably damaging 1.000 10/26/2016
29 437992 UTSW Slc37a1 0.117 R5609 G1 202 N 17 31338008 V383M G A missense Het possibly damaging 0.665 phenotype 10/26/2016
30 437974 UTSW Slc9a9 0.106 R5609 G1 225 N 9 94809937 Y182N T A missense Het probably damaging 0.996 phenotype 10/26/2016
31 437956 UTSW Slx4ip 0.164 R5609 G1 225 N 2 137000242 D29G A G missense Het probably damaging 1.000 10/26/2016
32 437962 UTSW St3gal5 0.169 R5609 G1 225 N 6 72153462 V319A T C missense Het possibly damaging 0.746 phenotype 10/26/2016
33 437997 UTSW Tbc1d10c 0.110 R5609 G1 225 N 19 4189882 M76I C T missense Het possibly damaging 0.892 phenotype 10/26/2016
34 437988 UTSW Thrb 0.313 R5609 G1 225 N 14 18033526 H416N C A missense Het probably benign 0.217 phenotype 10/26/2016
35 437984 UTSW Timp2 0.000 R5609 G1 225 N 11 118320161 D60V T A missense Het probably damaging 1.000 phenotype 10/26/2016
36 437994 UTSW Ubxn6 0.151 R5609 G1 95 N 17 56069745 E216K C T missense Het probably benign 0.399 10/26/2016
37 437986 UTSW Unc79 1.000 R5609 G1 225 N 12 103128268 M1977T T C missense Het probably benign 0.000 phenotype 10/26/2016
38 437968 UTSW Uri1 0.883 R5609 G1 225 N 7 37963529 R347* G A nonsense Het probably null phenotype 10/26/2016
39 437964 UTSW Vmn1r73 0.056 R5609 G1 225 N 7 11756664 W136* G A nonsense Het probably null 10/26/2016
40 457992 UTSW Vmn2r124 0.284 R5609 G1 225 N 17 18073840 Y730H T C missense Het probably benign 0.000 02/16/2017
41 437983 UTSW Wnk4 0.366 R5609 G1 225 N 11 101275636 C T unclassified Het probably benign phenotype 10/26/2016
42 437957 UTSW Zfhx4 0.508 R5609 G1 225 N 3 5403619 N2971D A G missense Het probably damaging 0.998 10/26/2016
[records 1 to 42 of 42]