Incidental Mutations

64 incidental mutations are currently displayed, and affect 64 genes.
9 are Possibly Damaging.
26 are Probably Damaging.
21 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 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 93065 APN Actn4 0.841 IGL01637 G1 7 28904684 (GRCm38) I384N A T missense Het probably damaging 1.000 phenotype 2013-12-09
2 93060 APN Adsl 1.000 IGL01637 G1 15 80948700 (GRCm38) Q51H G T missense Het probably null 0.240 phenotype 2013-12-09
3 93072 APN Apcdd1 0.165 IGL01637 G1 18 62937286 (GRCm38) E208G A G missense Het probably damaging 1.000 phenotype 2013-12-09
4 93082 APN Arrdc4 0.169 IGL01637 G1 7 68744832 (GRCm38) R155* G A nonsense Het probably null phenotype 2013-12-09
5 93032 APN Atp9b 0.095 IGL01637 G1 18 80756455 (GRCm38) E823G T C missense Het probably benign 0.058 2013-12-09
6 93083 APN Bmp1 1.000 IGL01637 G1 14 70492461 (GRCm38) W468R A G missense Het probably damaging 1.000 phenotype 2013-12-09
7 93081 APN C6 0.120 IGL01637 G1 15 4759917 (GRCm38) I281M A G missense Het possibly damaging 0.691 phenotype 2013-12-09
8 93067 APN Ccdc88b 0.000 IGL01637 G1 19 6846710 (GRCm38) T1392A T C missense Het probably benign 0.134 phenotype 2013-12-09
9 93071 APN Dhx34 0.444 IGL01637 G1 7 16205473 (GRCm38) S665Y G T missense Het probably damaging 1.000 phenotype 2013-12-09
10 93087 APN Dock1 1.000 IGL01637 G1 7 135137813 (GRCm38) A T critical splice acceptor site Het probably null phenotype 2013-12-09
11 93075 APN Dpp7 0.094 IGL01637 G1 2 25354613 (GRCm38) N252S T C missense Het probably benign 0.006 phenotype 2013-12-09
12 93037 APN Dyrk2 0.550 IGL01637 G1 10 118860507 (GRCm38) V282A A G missense Het probably damaging 0.995 phenotype 2013-12-09
13 93035 APN Edrf1 0.603 IGL01637 G1 7 133650525 (GRCm38) L401P T C missense Het probably damaging 1.000 phenotype 2013-12-09
14 93054 APN Epc1 1.000 IGL01637 G1 18 6439724 (GRCm38) V150A A G missense Het probably benign 0.224 phenotype 2013-12-09
15 93064 APN Fam170a 0.000 IGL01637 G1 18 50281667 (GRCm38) M127L A T missense Het possibly damaging 0.881 0.104 2013-12-09
16 93055 APN Fam19a3 0.032 IGL01637 G1 3 104773079 (GRCm38) V75M C T missense Het probably damaging 1.000 phenotype 2013-12-09
17 93070 APN Gabrg1 0.055 IGL01637 G1 5 70777205 (GRCm38) T277S T A missense Het probably damaging 0.995 phenotype 2013-12-09
18 93088 APN Galntl5 0.000 IGL01637 G1 5 25189825 (GRCm38) T C splice site Het probably benign phenotype 2013-12-09
19 93058 APN Gbp2b 0.000 IGL01637 G1 3 142598312 (GRCm38) N56S A G missense Het probably damaging 0.999 phenotype 2013-12-09
20 93073 APN Gfm2 0.660 IGL01637 G1 13 97150409 (GRCm38) V172E T A missense Het probably damaging 1.000 phenotype 2013-12-09
21 93051 APN Gm10419 IGL01637 G1 5 108372358 (GRCm38) T C unclassified Het probably benign 2013-12-09
22 93027 APN Gm7293 0.805 IGL01637 G1 9 51623606 (GRCm38) A G exon Het noncoding transcript 2013-12-09
23 93028 APN Gstm3 0.090 IGL01637 G1 3 107967633 (GRCm38) E101G T C missense Het probably damaging 1.000 2013-12-09
24 93079 APN Ifnlr1 0.000 IGL01637 G1 4 135686545 (GRCm38) W2R T C missense Het possibly damaging 0.630 phenotype 2013-12-09
25 93044 APN Ighv13-1 0.186 IGL01637 G1 12 114267733 (GRCm38) A T unclassified Het probably benign 2013-12-09
26 93041 APN Ighv7-1 0.083 IGL01637 G1 12 113896503 (GRCm38) I90F T A missense Het possibly damaging 0.780 2013-12-09
27 93068 APN Itga2b 0.287 IGL01637 G1 11 102455583 (GRCm38) L1009P A G missense Het probably damaging 1.000 phenotype 2013-12-09
28 93077 APN Kif1a 0.867 IGL01637 G1 1 93039853 (GRCm38) V1112A A G missense Het possibly damaging 0.952 phenotype 2013-12-09
29 93030 APN Kif5a 1.000 IGL01637 G1 10 127245368 (GRCm38) D232E A T missense Het possibly damaging 0.940 phenotype 2013-12-09
30 93085 APN Klb 0.889 IGL01637 G1 5 65375679 (GRCm38) G A critical splice acceptor site Het probably null phenotype 2013-12-09
31 93033 APN Lrriq1 0.069 IGL01637 G1 10 103215628 (GRCm38) A421V G A missense Het probably benign 0.000 2013-12-09
32 93074 APN Mdga1 0.262 IGL01637 G1 17 29839871 (GRCm38) R721C G A missense Het probably damaging 1.000 phenotype 2013-12-09
33 93089 APN Mrpl48 0.901 IGL01637 G1 7 100550532 (GRCm38) G T splice site Het probably benign phenotype 2013-12-09
34 93080 APN Myo18b 1.000 IGL01637 G1 5 112840629 (GRCm38) R1030S T A missense Het possibly damaging 0.817 phenotype 2013-12-09
35 93031 APN Nf1 1.000 IGL01637 G1 11 79547120 (GRCm38) H2101Q T A missense Het probably damaging 0.999 phenotype 2013-12-09
36 93047 APN Nlrp3 0.063 IGL01637 G1 11 59549378 (GRCm38) L594I C A missense Het probably damaging 0.992 phenotype 2013-12-09
37 93066 APN Notch2 1.000 IGL01637 G1 3 98146060 (GRCm38) T2013I C T missense Het probably damaging 1.000 phenotype 2013-12-09
38 93034 APN Olfr1018 0.076 IGL01637 G1 2 85822988 (GRCm38) T6S A T missense Het probably benign 0.003 phenotype 2013-12-09
39 93049 APN Olfr131 0.085 IGL01637 G1 17 38082103 (GRCm38) L292F G A missense Het possibly damaging 0.896 phenotype 2013-12-09
40 278721 APN Olfr593 0.051 IGL01637 G1 7 103212177 (GRCm38) R95S C A missense Het probably benign 0.000 phenotype 2015-04-16
41 93029 APN Olfr812 0.051 IGL01637 G1 10 129842610 (GRCm38) L144P A G missense Het probably benign 0.140 phenotype 2013-12-09
42 93040 APN Olfr845 0.114 IGL01637 G1 9 19338964 (GRCm38) F168S T C missense Het probably damaging 1.000 phenotype 2013-12-09
43 93053 APN Panx3 0.000 IGL01637 G1 9 37664056 (GRCm38) D170G T C missense Het probably damaging 0.976 phenotype 2013-12-09
44 93078 APN Pclo 0.000 IGL01637 G1 5 14540034 (GRCm38) S783G A G missense Het unknown phenotype 2013-12-09
45 93039 APN Pde3b 0.000 IGL01637 G1 7 114526901 (GRCm38) L790* T A nonsense Het probably null phenotype 2013-12-09
46 93086 APN Pik3r2 0.000 IGL01637 G1 8 70772348 (GRCm38) T C unclassified Het probably benign phenotype 2013-12-09
47 93063 APN Rassf4 0.069 IGL01637 G1 6 116641690 (GRCm38) F211L A G missense Het probably damaging 0.999 phenotype 2013-12-09
48 93056 APN Rbl2 1.000 IGL01637 G1 8 91106438 (GRCm38) P666S C T missense Het probably benign 0.000 phenotype 2013-12-09
49 93061 APN Rnf123 0.144 IGL01637 G1 9 108058238 (GRCm38) F979L A G missense Het probably damaging 0.997 phenotype 2013-12-09
50 93057 APN Rock2 0.847 IGL01637 G1 12 16965171 (GRCm38) D788E T A missense Het probably benign 0.000 phenotype 2013-12-09
51 93048 APN Serpina3b 0.065 IGL01637 G1 12 104132957 (GRCm38) T244A A G missense Het probably benign 0.003 2013-12-09
52 93059 APN Setd1b 1.000 IGL01637 G1 5 123148513 (GRCm38) S541P T C missense Het unknown phenotype 2013-12-09
53 93052 APN Slc12a4 0.311 IGL01637 G1 8 105960707 (GRCm38) D60G T C missense Het possibly damaging 0.718 phenotype 2013-12-09
54 93036 APN Stac2 0.164 IGL01637 G1 11 98041354 (GRCm38) E241G T C missense Het probably benign 0.004 2013-12-09
55 93076 APN Tas2r115 0.050 IGL01637 G1 6 132737629 (GRCm38) Y120H A G missense Het probably damaging 0.993 2013-12-09
56 93043 APN Tmtc2 0.108 IGL01637 G1 10 105370085 (GRCm38) F450I A T missense Het probably benign 0.003 phenotype 2013-12-09
57 93084 APN Txnl1 0.469 IGL01637 G1 18 63674191 (GRCm38) I198N A T missense Het probably damaging 0.978 2013-12-09
58 93046 APN Ubr2 0.859 IGL01637 G1 17 46956654 (GRCm38) M1049K A T missense Het probably damaging 0.998 phenotype 2013-12-09
59 93038 APN Ugt2b5 0.060 IGL01637 G1 5 87139900 (GRCm38) E136G T C missense Het probably benign 0.044 2013-12-09
60 93045 APN Unc13b 0.350 IGL01637 G1 4 43241066 (GRCm38) T3623I C T missense Het probably damaging 1.000 phenotype 2013-12-09
61 93062 APN Usp13 0.000 IGL01637 G1 3 32919064 (GRCm38) S797T T A missense Het probably benign 0.023 2013-12-09
62 93050 APN Vmn1r173 0.536 IGL01637 G1 7 23702948 (GRCm38) T203S A T missense Het probably damaging 0.959 2013-12-09
63 93042 APN Vwf 0.238 IGL01637 G1 6 125645736 (GRCm38) I1718N T A missense Het probably damaging 1.000 phenotype 2013-12-09
64 93069 APN Zfr 1.000 IGL01637 G1 15 12159646 (GRCm38) H676R A G missense Het probably benign 0.260 phenotype 2013-12-09
[records 1 to 64 of 64]