Incidental Mutations

64 incidental mutations are currently displayed, and affect 64 genes.
9 are Possibly Damaging.
20 are Probably Damaging.
27 are Probably Benign.
7 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 64 of 64] 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 306491 APN 4930572O03Rik IGL00088 G1 5 15656886 C A utr 5 prime Het probably benign 04/16/2015
2 747 APN Ankhd1 0.000 IGL00088 G1 18 36665459 A G unclassified Het probably benign 07/12/2011
3 1481 APN Anpep 0.000 IGL00088 G1 7 79825736 V879A A G missense Het possibly damaging 0.643 phenotype 07/12/2011
4 1045 APN Asb13 0.109 IGL00088 G1 13 3643476 V78G T G missense Het probably null 0.996 phenotype 07/12/2011
5 1096 APN Atad2b 0.000 IGL00088 G1 12 5024593 R1051G A G missense Het probably damaging 0.999 phenotype 07/12/2011
6 996 APN Bdp1 1.000 IGL00088 G1 13 100098510 Y192C T C missense Het probably damaging 1.000 phenotype 07/12/2011
7 1963 APN C1ql2 0.093 IGL00088 G1 1 120341670 G185C G T missense Het probably damaging 1.000 07/12/2011
8 1724 APN C87499 0.306 IGL00088 G1 4 88629070 K121N T A missense Het probably benign 0.434 07/12/2011
9 1514 APN Catsperg2 0.085 IGL00088 G1 7 29705404 S745P A G missense Het possibly damaging 0.856 07/12/2011
10 2007 APN Col19a1 1.000 IGL00088 G1 1 24561306 S52T A T missense Het unknown phenotype 07/12/2011
11 1415 APN Col4a2 1.000 IGL00088 G1 8 11443685 G1418V G T missense Het probably damaging 1.000 phenotype 07/12/2011
12 1834 APN Crnkl1 0.962 IGL00088 G1 2 145918468 D677N C T missense Het possibly damaging 0.754 phenotype 07/12/2011
13 306486 APN Cyp2j8 0.078 IGL00088 G1 4 96503842 N125I T A missense Het probably benign 0.063 04/16/2015
14 1521 APN Cyp2t4 0.077 IGL00088 G1 7 27155298 M68L A T missense Het probably benign 0.001 07/12/2011
15 1782 APN Dclk2 0.000 IGL00088 G1 3 86799090 T A critical splice acceptor site Het probably null phenotype 07/12/2011
16 1310 APN Dmxl2 1.000 IGL00088 G1 9 54401704 D1921G T C missense Het probably benign 0.000 phenotype 07/12/2011
17 1624 APN Dnah10 0.178 IGL00088 G1 5 124828603 G4104S G A missense Het probably damaging 1.000 phenotype 07/12/2011
18 1714 APN Echdc2 0.095 IGL00088 G1 4 108178911 I273T T C missense Het probably damaging 1.000 07/12/2011
19 1696 APN Extl1 0.322 IGL00088 G1 4 134358019 K596E T C missense Het probably damaging 0.999 phenotype 07/12/2011
20 715 APN Fads3 0.000 IGL00088 G1 19 10052299 D108V A T missense Het probably null 0.981 phenotype 07/12/2011
21 917 APN Fam135b 0.000 IGL00088 G1 15 71450494 L1274P A G missense Het probably damaging 1.000 07/12/2011
22 306485 APN Fat1 1.000 IGL00088 G1 8 45024602 H2228Q T A missense Het possibly damaging 0.931 phenotype 04/16/2015
23 1245 APN Gcc2 0.216 IGL00088 G1 10 58292680 H1341Y C T missense Het probably damaging 0.997 phenotype 07/12/2011
24 1213 APN Gls2 0.000 IGL00088 G1 10 128200971 A G unclassified 1691 bp Het probably null phenotype 07/12/2011
25 1690 APN Gm13119 0.000 IGL00088 G1 4 144362530 H139Q T A missense Het possibly damaging 0.912 07/12/2011
26 719 APN Gpr137 0.000 IGL00088 G1 19 6939704 V139G A C missense Het probably damaging 0.998 07/12/2011
27 1955 APN Ikbke 0.000 IGL00088 G1 1 131270012 A G splice site 6 bp Het probably null phenotype 07/12/2011
28 1564 APN Irak2 0.000 IGL00088 G1 6 113678675 N285Y A T missense Het probably benign 0.405 phenotype 07/12/2011
29 1405 APN Kcnu1 0.000 IGL00088 G1 8 25897856 C566Y G A missense Het probably benign 0.001 phenotype 07/12/2011
30 1095 APN Klhl29 0.155 IGL00088 G1 12 5140705 P97S G A missense Het probably benign 0.009 07/12/2011
31 1257 APN Lama4 1.000 IGL00088 G1 10 39065595 T C splice site Het probably benign phenotype 07/12/2011
32 1900 APN Lhx6 0.800 IGL00088 G1 2 36091716 G A splice site Het probably benign phenotype 07/12/2011
33 306488 APN Mdn1 1.000 IGL00088 G1 4 32723651 L2529P T C missense Het probably damaging 1.000 04/16/2015
34 306487 APN Muc4 0.088 IGL00088 G1 16 32754086 G1321R G A missense Het probably benign 0.354 phenotype 04/16/2015
35 1793 APN Naa15 0.962 IGL00088 G1 3 51438405 V19D T A missense Het probably damaging 1.000 phenotype 07/12/2011
36 1162 APN Ncbp3 0.094 IGL00088 G1 11 73073529 A T splice site Het probably benign 07/12/2011
37 1274 APN Nckipsd 0.314 IGL00088 G1 9 108814969 V530I G A missense Het probably benign 0.068 phenotype 07/12/2011
38 1895 APN Neb 0.790 IGL00088 G1 2 52308747 I394T A G missense Het possibly damaging 0.545 0.070 phenotype 07/12/2011
39 28102 APN Nnmt 0.000 IGL00088 G1 9 48591924 A T utr 3 prime Het probably benign phenotype 04/17/2013
40 953 APN Nupl1 0.944 IGL00088 G1 14 60242577 I207L T A missense Het probably benign 0.009 phenotype 07/12/2011
41 306483 APN Olfr113 0.120 IGL00088 G1 17 37574917 C169S A T missense Het probably damaging 0.979 phenotype 04/16/2015
42 843 APN Olfr180 0.091 IGL00088 G1 16 58915850 E264K C T missense Het probably benign 0.007 phenotype 07/12/2011
43 1476 APN Olfr290 0.188 IGL00088 G1 7 84916370 M197K T A missense Het probably damaging 0.990 phenotype 07/12/2011
44 306484 APN Otud4 0.144 IGL00088 G1 8 79672881 N741K T A missense Het probably damaging 0.987 phenotype 04/16/2015
45 1368 APN Pard6a 0.461 IGL00088 G1 8 105703201 C264S T A missense Het probably benign 0.001 phenotype 07/12/2011
46 306489 APN Plch2 0.000 IGL00088 G1 4 155006642 N276S T C missense Het probably damaging 1.000 phenotype 04/16/2015
47 885 APN Racgap1 1.000 IGL00088 G1 15 99636122 T C unclassified Het probably benign phenotype 07/12/2011
48 1147 APN Rad51d 1.000 IGL00088 G1 11 82889746 D70G T C missense Het probably damaging 0.999 phenotype 07/12/2011
49 906 APN Recql4 1.000 IGL00088 G1 15 76707336 A484T C T missense Het possibly damaging 0.521 phenotype 07/12/2011
50 1570 APN Reg3g 0.000 IGL00088 G1 6 78466779 S149T A T missense Het probably benign 0.000 phenotype 07/12/2011
51 1494 APN Rpl13a 0.946 IGL00088 G1 7 45127071 C A unclassified Het probably null phenotype 07/12/2011
52 306490 APN Scn10a 0.256 IGL00088 G1 9 119672226 Y164C T C missense Het probably damaging 1.000 phenotype 04/16/2015
53 1890 APN Scn2a 1.000 IGL00088 G1 2 65764440 I1878V A G missense Het probably benign 0.000 phenotype 07/12/2011
54 947 APN Sgcg 0.153 IGL00088 G1 14 61240347 R98* T A nonsense Het probably null phenotype 07/12/2011
55 1585 APN Tas2r137 0.068 IGL00088 G1 6 40491340 I35F A T missense Het probably benign 0.202 phenotype 07/12/2011
56 1099 APN Tex19.2 0.175 IGL00088 G1 11 121116812 F270S A G missense Het possibly damaging 0.930 Tex19.1 causes testis degeneration and male infertility owing to meiotic arrest in the germ cells. [provided by MGI curators] (source: MGI)">phenotype 07/12/2011
57 1279 APN Traip 1.000 IGL00088 G1 9 107970550 R391W C T missense Het probably benign 0.154 phenotype 07/12/2011
58 1179 APN Trim7 0.093 IGL00088 G1 11 48845571 N251D A G missense Het probably damaging 0.993 phenotype 07/12/2011
59 861 APN Trmt2a 0.000 IGL00088 G1 16 18249487 V8D T A missense Het probably benign 0.000 phenotype 07/12/2011
60 1883 APN Ubr3 1.000 IGL00088 G1 2 69988810 I9L A C missense Het probably benign 0.402 phenotype 07/12/2011
61 1601 APN Usp42 0.000 IGL00088 G1 5 143717142 S575P A G missense Het probably benign 0.003 phenotype 07/12/2011
62 1536 APN Vmn2r52 0.134 IGL00088 G1 7 10169096 H468Q G T missense Het probably benign 0.297 07/12/2011
63 1502 APN Vmn2r59 0.073 IGL00088 G1 7 42012064 T776S T A missense Het possibly damaging 0.907 07/12/2011
64 1017 APN Zcchc6 0.645 IGL00088 G1 13 59816698 E221G T C missense Het probably damaging 1.000 07/12/2011
[records 1 to 64 of 64]