Incidental Mutations

43 incidental mutations are currently displayed, and affect 43 genes.
6 are Possibly Damaging.
14 are Probably Damaging.
16 are Probably Benign.
7 are Probably Null.
3 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 43 of 43] 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 77007 UTSW Abcb1b 0.290 R0847 G1 225 N 5 8845764 I899T T C missense Het probably damaging 0.994 phenotype 10/16/2013
2 77037 UTSW Ahnak 0.292 R0847 G1 225 N 19 9006433 Q1694* C T nonsense Het probably null phenotype 10/16/2013
3 77002 UTSW AI314180 0.389 R0847 G1 225 N 4 58841439 T645I G A missense Het probably benign 0.143 10/16/2013
4 77013 UTSW Cblc 0.000 R0847 G1 225 N 7 19790534 Y260* A T nonsense Het probably null phenotype 10/16/2013
5 77012 UTSW Ceacam5 0.061 R0847 G1 225 N 7 17757837 T711A A G missense Het possibly damaging 0.707 10/16/2013
6 77021 UTSW Cep63 0.604 R0847 G1 225 N 9 102588758 S690P A G missense Het probably benign 0.117 phenotype 10/16/2013
7 76997 UTSW Chia1 0.544 R0847 G1 225 N 3 106131937 I448F A T missense Het probably benign 0.115 phenotype 10/16/2013
8 77020 UTSW Dmxl2 1.000 R0847 G1 225 N 9 54405828 F1712I A T missense Het probably damaging 1.000 phenotype 10/16/2013
9 77001 UTSW Exosc3 0.960 R0847 G1 225 N 4 45319695 V109A A G missense Het probably damaging 1.000 phenotype 10/16/2013
10 77014 UTSW Fxyd7 0.000 R0847 G1 225 N 7 31044604 C60R A G missense Het probably damaging 0.991 phenotype 10/16/2013
11 77033 UTSW Gm17349 R0847 G1 181 N 15 99702408 C A unclassified Het probably benign 10/16/2013
12 77005 UTSW Gpn2 0.962 R0847 G1 225 N 4 133588595 N199D A G missense Het probably benign 0.406 10/16/2013
13 76999 UTSW Ints12 1.000 R0847 G1 225 N 3 133108842 T270M C T missense Het possibly damaging 0.721 phenotype 10/16/2013
14 77003 UTSW Kdm4a 0.837 R0847 G1 225 N 4 118164498 E266K C T missense Het probably damaging 0.959 phenotype 10/16/2013
15 77034 UTSW Kremen2 0.098 R0847 G1 222 N 17 23744660 T50N G T missense Het probably damaging 0.997 phenotype 10/16/2013
16 77004 UTSW Macf1 1.000 R0847 G1 225 N 4 123399366 D1249E A T missense Het probably benign 0.026 phenotype 10/16/2013
17 77028 UTSW Mdga2 0.000 R0847 G1 225 N 12 66723080 K146N T A missense Het probably damaging 0.999 phenotype 10/16/2013
18 77036 UTSW Med20 1.000 R0847 G1 225 N 17 47611693 G A critical splice donor site 1 bp Het probably null phenotype 10/16/2013
19 77010 UTSW Myo18b 1.000 R0847 G1 225 N 5 112874488 T C unclassified Het probably benign phenotype 10/16/2013
20 77026 UTSW Nav3 0.000 R0847 G1 225 N 10 109903857 T84S T A missense Het possibly damaging 0.942 phenotype 10/16/2013
21 77019 UTSW Olfm2 0.100 R0847 G1 225 N 9 20668657 V266A A G missense Het probably damaging 0.998 phenotype 10/16/2013
22 77038 UTSW Olfr1453 0.098 R0847 G1 225 N 19 13027731 Y199* A T nonsense Het probably null phenotype 10/16/2013
23 77039 UTSW Olfr1487 0.079 R0847 G1 225 N 19 13619551 H87Y C T missense Het probably benign 0.098 phenotype 10/16/2013
24 77027 UTSW Olfr810 0.088 R0847 G1 225 N 10 129791458 I44F T A missense Het probably damaging 1.000 phenotype 10/16/2013
25 77011 UTSW Pthlh 1.000 R0847 G1 199 N 6 147263268 A T critical splice donor site 2 bp Het probably null phenotype 10/16/2013
26 77032 UTSW Rpap3 1.000 R0847 G1 198 N 15 97703201 C T critical splice donor site 1 bp Het probably null phenotype 10/16/2013
27 76996 UTSW Rprd2 0.589 R0847 G1 225 N 3 95765413 S893P A G missense Het probably benign 0.003 10/16/2013
28 77022 UTSW Sacm1l 1.000 R0847 G1 225 N 9 123548862 G69D G A missense Het probably damaging 0.999 phenotype 10/16/2013
29 76994 UTSW Slc27a4 1.000 R0847 G1 225 N 2 29811249 S351P T C missense Het probably benign 0.204 phenotype 10/16/2013
30 77023 UTSW Sobp 0.720 R0847 G1 225 N 10 43022419 R390P C G missense Het probably damaging 0.999 phenotype 10/16/2013
31 77029 UTSW Spata7 0.122 R0847 G1 225 N 12 98648430 M107K T A missense Het possibly damaging 0.821 phenotype 10/16/2013
32 77006 UTSW Sri 0.260 R0847 G1 225 N 5 8063755 G A splice site 5 bp Het probably null phenotype 10/16/2013
33 77025 UTSW Stab2 0.000 R0847 G1 225 N 10 86969871 I204V T C missense Het probably benign 0.001 phenotype 10/16/2013
34 77017 UTSW Synm 0.000 R0847 G1 225 N 7 67735056 I511V T C missense Het probably damaging 0.999 phenotype 10/16/2013
35 76995 UTSW Tbr1 1.000 R0847 G1 225 N 2 61805029 S108P T C missense Het probably benign 0.002 phenotype 10/16/2013
36 77000 UTSW Tln1 1.000 R0847 G1 225 N 4 43555333 F197S A G missense Het probably damaging 0.999 phenotype 10/16/2013
37 76998 UTSW Tmem167b 0.186 R0847 G1 225 N 3 108560221 G46R C T missense Het probably benign 0.000 10/16/2013
38 77009 UTSW Tmprss11g 0.071 R0847 G1 225 N 5 86490726 K301R T C missense Het probably benign 0.006 10/16/2013
39 77035 UTSW Tnfrsf21 0.142 R0847 G1 225 N 17 43038213 H239Y C T missense Het probably benign 0.000 0.068 phenotype 10/16/2013
40 77024 UTSW Trpm2 0.142 R0847 G1 225 N 10 77929288 V960M C T missense Het possibly damaging 0.941 phenotype 10/16/2013
41 77016 UTSW Ube3a 0.584 R0847 G1 225 N 7 59276586 D371N G A missense Het possibly damaging 0.798 phenotype 10/16/2013
42 77015 UTSW Vmn2r57 0.122 R0847 G1 225 N 7 41428801 F78I A T missense Het probably benign 0.002 10/16/2013
43 77030 UTSW Wisp1 0.089 R0847 G1 225 N 15 66919275 C309G T G missense Het probably damaging 1.000 phenotype 10/16/2013
[records 1 to 43 of 43]