Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
4 are Possibly Damaging.
13 are Probably Damaging.
15 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 37 of 37] 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 44629 UTSW Ahsa1 0.000 V8831 225 N 710 12 87269923 N107S A G missense Het probably damaging 1.000 06/11/2013
2 44625 UTSW Arhgap23 0.000 V8831 225 N 710 11 97456545 I690V A G missense Het probably benign 0.002 phenotype 06/11/2013
3 44606 UTSW Bard1 1.000 V8831 225 N 710 1 71088217 P78S G A missense Het probably damaging 1.000 phenotype 06/11/2013
4 44623 UTSW Ccar1 0.937 V8831 225 N 710 10 62747406 T976I G A missense Het unknown 06/11/2013
5 44612 UTSW Cdc7 1.000 V8831 209 N 710 5 106968910 N50K T A missense Het probably benign 0.009 phenotype 06/11/2013
6 44609 UTSW Cep85 0.950 V8831 225 N 710 4 134156069 E170K C T missense Het possibly damaging 0.938 phenotype 06/11/2013
7 44630 UTSW Cpsf2 0.966 V8831 225 N 710 12 102003141 R757C C T missense Het probably damaging 1.000 06/11/2013
8 44633 UTSW Csmd3 0.000 V8831 226 N 710 15 48457696 D239E A T missense Het probably damaging 0.963 06/11/2013
9 44604 UTSW Dnah7b 0.141 V8831 225 N 710 1 46373298 Y4022* T G nonsense Het probably null 06/11/2013
10 44618 UTSW Elmo3 0.000 V8831 225 N 710 8 105307061 N179S A G missense Het probably benign 0.243 phenotype 06/11/2013
11 44640 UTSW H2-T24 0.000 V8831 225 N 710 17 36017324 Q89L T A missense Het probably damaging 0.961 06/11/2013
12 44632 UTSW Hist1h2bj 0.252 V8831 225 N 710 13 22043281 G C unclassified Het probably benign phenotype 06/11/2013
13 44635 UTSW Irak4 0.823 V8831 225 N 710 15 94561484 I327T T C missense Het probably damaging 0.995 0.385 phenotype 06/11/2013
14 44615 UTSW Itpr2 0.000 V8831 225 N 710 6 146385882 L157Q A T missense Het probably damaging 1.000 phenotype 06/11/2013
15 44641 UTSW Lama1 1.000 V8831 225 N 710 17 67752883 D656N G A missense Het probably benign 0.001 phenotype 06/11/2013
16 44627 UTSW Lrrc72 0.072 V8831 225 N 710 12 36208657 T67K G T missense Het possibly damaging 0.655 06/11/2013
17 44605 UTSW Map2 0.813 V8831 225 N 710 1 66415845 I1298S T G missense Het probably damaging 1.000 phenotype 06/11/2013
18 66995 UTSW Mroh2a 0.951 V8831 217 N 710 1 88256167 T TN frame shift Het probably null phenotype 08/20/2013
19 44642 UTSW Ndst1 1.000 V8831 225 N 710 18 60702927 A428V G A missense Het probably damaging 0.995 phenotype 06/11/2013
20 44607 UTSW Obsl1 0.271 V8831 213 N 710 1 75486756 T1764M G A missense Het probably benign 0.000 0.090 06/11/2013
21 44631 UTSW Olfr1369-ps1 0.259 V8831 225 N 710 13 21116003 Y104H T C missense Het possibly damaging 0.934 06/11/2013
22 44638 UTSW Olfr177 0.078 V8831 225 N 710 16 58873075 T25K G T missense Het probably benign 0.283 phenotype 06/11/2013
23 44617 UTSW Olfr481 0.067 V8831 225 N 710 7 108081535 A247V C T missense Het probably benign 0.238 phenotype 06/11/2013
24 44614 UTSW Plxna1 0.868 V8831 225 N 710 6 89357137 V170A A G missense Het probably damaging 0.993 phenotype 06/11/2013
25 44622 UTSW Rfx6 1.000 V8831 225 N 710 10 51718208 G A critical splice donor site 1 bp Het probably null phenotype 06/11/2013
26 44621 UTSW Shprh 0.000 V8831 182 N 710 10 11186862 D1238N G A missense Het probably damaging 1.000 Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators] (source: MGI)">phenotype 06/11/2013
27 44636 UTSW Slc15a2 0.110 V8831 225 N 710 16 36772445 M179T A G missense Het probably benign 0.000 phenotype 06/11/2013
28 44637 UTSW Slc9c1 0.452 V8831 225 N 710 16 45577899 I676F A T missense Het possibly damaging 0.894 phenotype 06/11/2013
29 44628 UTSW Smoc1 1.000 V8831 225 N 710 12 81168255 D305G A G missense Het probably damaging 0.998 phenotype 06/11/2013
30 44639 UTSW Spdef 0.720 V8831 225 N 710 17 27718077 R184H C T missense Het probably damaging 1.000 phenotype 06/11/2013
31 44624 UTSW Stxbp4 0.000 V8831 225 N 710 11 90480671 A535T C T missense Het probably benign 0.342 06/11/2013
32 44608 UTSW Tcp11l1 0.138 V8831 225 N 710 2 104685484 V345L C G missense Het probably benign 0.000 06/11/2013
33 66996 UTSW Ticam1 0.000 V8831 217 N 710 17 56269969 TC T frame shift Het probably null phenotype 08/20/2013
34 44613 UTSW Ttc28 0.000 V8831 225 N 710 5 111100712 Y177F A T missense Het probably benign 0.114 06/11/2013
35 44611 UTSW Ugt2b34 0.107 V8831 225 N 710 5 86906674 Y83N A T missense Het probably benign 0.390 06/11/2013
36 44616 UTSW Vmn2r30 V8831 225 N 710 7 7334149 R163C G A missense Het probably benign 0.002 06/11/2013
37 44620 UTSW Xirp1 0.278 V8831 225 N 710 9 120016907 Q970P T G missense Het probably benign 0.000 phenotype 06/11/2013
[records 1 to 37 of 37]