Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
1 are Possibly Damaging.
13 are Probably Damaging.
12 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 157622 UTSW 1700021F07Rik 0.053 R1319 G1 225 N 2 173527923 (GRCm38) S77C A T missense Het probably damaging 0.981 2014-02-18
2 157644 UTSW Adam28 0.159 R1319 G1 225 N 14 68609129 (GRCm38) E745G T C missense Het probably benign 0.278 phenotype 2014-02-18
3 157645 UTSW Adamts12 0.095 R1319 G1 225 N 15 11286791 (GRCm38) K827N G T missense Het probably benign 0.021 phenotype 2014-02-18
4 157643 UTSW Ang2 0.062 R1319 G1 225 N 14 51195707 (GRCm38) T73A T C missense Het probably benign 0.024 2014-02-18
5 157638 UTSW Bbs10 1.000 R1319 G1 155 N 10 111298874 (GRCm38) L51P T C missense Het probably damaging 1.000 phenotype 2014-02-18
6 157633 UTSW Bean1 0.000 R1319 G1 225 N 8 104217224 (GRCm38) I137T T C missense Het probably benign 0.000 phenotype 2014-02-18
7 157628 UTSW Cttnbp2 0.000 R1319 G1 225 N 6 18434630 (GRCm38) T410A T C missense Het probably benign 0.001 phenotype 2014-02-18
8 157626 UTSW Cyp4a10 0.082 R1319 G1 225 N 4 115521145 (GRCm38) I143L A C missense Het probably damaging 0.978 phenotype 2014-02-18
9 157631 UTSW Dlg2 0.000 R1319 G1 225 N 7 92438023 (GRCm38) Q788L A T missense Het probably damaging 0.977 phenotype 2014-02-18
10 157627 UTSW Epha10 0.000 R1319 G1 225 N 4 124881914 (GRCm38) V14I G A missense Het probably benign 0.000 phenotype 2014-02-18
11 157620 UTSW Eprs 1.000 R1319 G1 225 N 1 185384962 (GRCm38) D401N G A missense Het probably damaging 1.000 phenotype 2014-02-18
12 157642 UTSW Fam169a 0.077 R1319 G1 225 N 13 97097562 (GRCm38) V114A T C missense Het probably damaging 0.996 2014-02-18
13 157649 UTSW Fbn2 0.902 R1319 G1 225 N 18 58200610 (GRCm38) P178S G A missense Het possibly damaging 0.880 phenotype 2014-02-18
14 157624 UTSW Fcrls 0.053 R1319 G1 124 N 3 87262177 (GRCm38) A C critical splice donor site 2 bp Het probably null phenotype 2014-02-18
15 157635 UTSW Grm1 0.389 R1319 G1 119 N 10 10689398 (GRCm38) H1055Q G T missense Het probably benign 0.047 phenotype 2014-02-18
16 157619 UTSW Mcm6 1.000 R1319 G1 215 N 1 128349052 (GRCm38) N267S T C missense Het probably benign 0.000 phenotype 2014-02-18
17 157650 UTSW Olfr262 0.100 R1319 G1 225 N 19 12241502 (GRCm38) D53G T C missense Het probably damaging 0.997 phenotype 2014-02-18
18 157623 UTSW Phc3 0.000 R1319 G1 225 N 3 30929869 (GRCm38) I699V T C missense Het probably damaging 0.971 2014-02-18
19 157641 UTSW Prl2c2 0.148 R1319 G1 156 N 13 13002201 (GRCm38) T47R G C missense Het probably damaging 0.983 0.647 2014-02-18
20 157629 UTSW Pyroxd1 1.000 R1319 G1 210 N 6 142359148 (GRCm38) V367A T C missense Het probably benign 0.331 2014-02-18
21 157618 UTSW R3hdm1 0.000 R1319 G1 225 N 1 128231405 (GRCm38) R939H G A missense Het probably benign 0.009 2014-02-18
22 157621 UTSW Rag1 0.509 R1319 G1 225 N 2 101643192 (GRCm38) I535N A T missense Het probably damaging 0.997 phenotype 2014-02-18
23 157640 UTSW Rhot1 1.000 R1319 G1 225 N 11 80246021 (GRCm38) C310R T C missense Het probably damaging 0.982 phenotype 2014-02-18
24 157632 UTSW Tnrc6a 0.821 R1319 G1 225 N 7 123184251 (GRCm38) V1481M G A missense Het probably benign 0.017 phenotype 2014-02-18
25 157646 UTSW Vmn1r234 0.051 R1319 G1 225 N 17 21228910 (GRCm38) M29L A T missense Het probably benign 0.011 2014-02-18
26 157630 UTSW Vmn2r68 0.073 R1319 G1 225 N 7 85232492 (GRCm38) I460T A G missense Het probably damaging 0.959 2014-02-18
27 157634 UTSW Zfhx3 0.924 R1319 G1 202 N 8 108933833 (GRCm38) Y1240N T A missense Het probably damaging 0.993 phenotype 2014-02-18
[records 1 to 27 of 27]