Incidental Mutations

49 incidental mutations are currently displayed, and affect 49 genes.
8 are Possibly Damaging.
19 are Probably Damaging.
14 are Probably Benign.
7 are Probably Null.
2 create premature stop codons.
4 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 49 of 49] 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 280031 APN Adam29 0.100 IGL02108 8 55872311 I369M T C missense Het probably damaging 0.978 phenotype 04/16/2015
2 280051 APN Aff1 0.334 IGL02108 5 103811109 T G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
3 280043 APN Arid1a 1.000 IGL02108 4 133680516 P2227T G T missense Het unknown phenotype 04/16/2015
4 280045 APN Atp12a 0.000 IGL02108 14 56384068 D720V A T missense Het possibly damaging 0.947 0.128 phenotype 04/16/2015
5 280054 APN Auh 0.000 IGL02108 13 52889097 T C splice site Het probably benign phenotype 04/16/2015
6 280021 APN Bptf 1.000 IGL02108 11 107074988 V1012L C A missense Het probably benign 0.448 phenotype 04/16/2015
7 280042 APN Cbr1 0.150 IGL02108 16 93610199 F268L T C missense Het probably benign 0.028 phenotype 04/16/2015
8 280016 APN Ccdc190 0.109 IGL02108 1 169933986 D219G A G missense Het probably damaging 0.993 04/16/2015
9 280055 APN Ccnb1 1.000 IGL02108 13 100781157 C T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
10 280041 APN Cdh19 0.000 IGL02108 1 110889731 S760R G T missense Het probably benign 0.315 phenotype 04/16/2015
11 280056 APN Cecr2 1.000 IGL02108 6 120762558 G A critical splice donor site 1 bp Het probably null phenotype 04/16/2015
12 280011 APN Chid1 0.077 IGL02108 7 141532928 M1K A T start codon destroyed Het probably null 0.984 04/16/2015
13 280048 APN Dzank1 0.000 IGL02108 2 144506223 T208A T C missense Het probably benign 0.023 phenotype 04/16/2015
14 280044 APN Ecm2 0.169 IGL02108 13 49518444 Y140* T A nonsense Het probably null phenotype 04/16/2015
15 280014 APN Enox2 IGL02108 X 49013516 L533S A G missense Het possibly damaging 0.743 phenotype 04/16/2015
16 280019 APN Fntb 1.000 IGL02108 12 76887857 E167G A G missense Het possibly damaging 0.626 phenotype 04/16/2015
17 280046 APN Gpihbp1 0.000 IGL02108 15 75597612 V92A T C missense Het probably benign 0.332 phenotype 04/16/2015
18 280049 APN Grsf1 0.000 IGL02108 5 88665903 R329Q C T missense Het probably benign 0.348 phenotype 04/16/2015
19 280013 APN Gtpbp4 0.966 IGL02108 13 8985213 D370V T A missense Het probably benign 0.203 phenotype 04/16/2015
20 280047 APN Hist1h2ab IGL02108 13 23751224 V31A T C missense Het probably benign 0.355 phenotype 04/16/2015
21 280017 APN Klhl14 0.490 IGL02108 18 21557920 Y491F T A missense Het probably damaging 0.984 phenotype 04/16/2015
22 280028 APN Lamb3 0.231 IGL02108 1 193332222 Q563L A T missense Het probably damaging 1.000 phenotype 04/16/2015
23 280039 APN Lcn2 0.000 IGL02108 2 32387605 L124Q A T missense Het probably damaging 0.989 phenotype 04/16/2015
24 280030 APN Mbl1 0.000 IGL02108 14 41153651 S21P T C missense Het possibly damaging 0.734 phenotype 04/16/2015
25 280053 APN Myrip 0.000 IGL02108 9 120467565 G A critical splice donor site 1 bp Het probably null 04/16/2015
26 280032 APN Nmur2 0.106 IGL02108 11 56040364 T174A T C missense Het probably benign 0.329 phenotype 04/16/2015
27 280050 APN Odf1 0.063 IGL02108 15 38226379 Y174* C A nonsense Het probably null phenotype 04/16/2015
28 280027 APN Olfr1024 0.081 IGL02108 2 85904150 D301E A T missense Het possibly damaging 0.671 phenotype 04/16/2015
29 280012 APN Olfr877 0.076 IGL02108 9 37854938 V40E T A missense Het possibly damaging 0.883 phenotype 04/16/2015
30 280009 APN Olfr969 0.229 IGL02108 9 39795512 I46F A T missense Het probably damaging 0.993 phenotype 04/16/2015
31 280026 APN Optn 0.223 IGL02108 2 5031273 V466A A G missense Het possibly damaging 0.907 phenotype 04/16/2015
32 280025 APN Pde9a 0.412 IGL02108 17 31461693 S316N G A missense Het probably benign 0.000 phenotype 04/16/2015
33 280037 APN Phf3 0.000 IGL02108 1 30829951 I672K A T missense Het probably damaging 1.000 phenotype 04/16/2015
34 280036 APN Pklr 0.351 IGL02108 3 89137403 I63F A T missense Het probably damaging 1.000 phenotype 04/16/2015
35 280057 APN Plet1 0.000 IGL02108 9 50499087 T C splice site Het probably benign 04/16/2015
36 280029 APN Pp2d1 0.061 IGL02108 17 53515405 D211V T A missense Het probably damaging 1.000 04/16/2015
37 280023 APN Ppp6r3 0.893 IGL02108 19 3492494 W384R A T missense Het probably damaging 1.000 phenotype 04/16/2015
38 280034 APN Prdm11 0.490 IGL02108 2 92975703 I301V T C missense Het probably damaging 0.997 04/16/2015
39 280010 APN Prkar1a 1.000 IGL02108 11 109667525 R357C C T missense Het probably damaging 1.000 phenotype 04/16/2015
40 280015 APN Ptchd1 0.000 IGL02108 X 155573552 T886A T C missense Het probably damaging 0.988 phenotype 04/16/2015
41 280040 APN Ptpre 0.662 IGL02108 7 135659102 E156V A T missense Het possibly damaging 0.846 phenotype 04/16/2015
42 280035 APN Ptprq 0.394 IGL02108 10 107646617 T1032A T C missense Het probably damaging 1.000 phenotype 04/16/2015
43 280020 APN Rras2 0.320 IGL02108 7 114060388 I47T A G missense Het probably damaging 1.000 phenotype 04/16/2015
44 280024 APN Setdb2 0.555 IGL02108 14 59402315 R709Q C T missense Het probably damaging 1.000 phenotype 04/16/2015
45 280022 APN Sh3rf3 0.157 IGL02108 10 59135828 V826E T A missense Het probably damaging 0.999 04/16/2015
46 280018 APN Tmem127 0.000 IGL02108 2 127257106 S132T T A missense Het probably damaging 0.980 phenotype 04/16/2015
47 280038 APN Tnrc6c 0.000 IGL02108 11 117721199 P221Q C A missense Het probably benign 0.293 phenotype 04/16/2015
48 280052 APN Tstd3 0.093 IGL02108 4 21759366 A T intron Het probably benign 04/16/2015
49 280033 APN Usp46 0.182 IGL02108 5 74029206 T55P T G missense Het probably damaging 1.000 phenotype 04/16/2015
[records 1 to 49 of 49]