Incidental Mutations

49 incidental mutations are currently displayed, and affect 49 genes.
9 are Possibly Damaging.
16 are Probably Damaging.
16 are Probably Benign.
6 are Probably Null.
4 create premature stop codons.
2 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 294156 APN 0610009O20Rik 0.285 IGL02456 18 38261124 (GRCm38) L458Q T A missense Het probably damaging 1.000 2015-04-16
2 294166 APN 4921511C20Rik IGL02456 X 127394961 (GRCm38) Y174* T A nonsense Het probably null 2015-04-16
3 294164 APN Apc 0.970 IGL02456 18 34313882 (GRCm38) S1243* C A nonsense Het probably null phenotype 2015-04-16
4 294186 APN Atp8b5 0.074 IGL02456 4 43365578 (GRCm38) T731A A G missense Het probably benign 0.163 2015-04-16
5 294149 APN Bcl2a1c 0.297 IGL02456 9 114330390 (GRCm38) F79I T A missense Het probably damaging 1.000 2015-04-16
6 294184 APN Brip1 0.000 IGL02456 11 86065099 (GRCm38) L863I G T missense Het possibly damaging 0.707 phenotype 2015-04-16
7 294152 APN Cbx4 1.000 IGL02456 11 119082112 (GRCm38) K146* T A nonsense Het probably null phenotype 2015-04-16
8 294179 APN Ccdc36 0.127 IGL02456 9 108406621 (GRCm38) T208K G T missense Het probably benign 0.001 2015-04-16
9 294170 APN Ces1a 0.000 IGL02456 8 93039498 (GRCm38) V163I C T missense Het possibly damaging 0.565 2015-04-16
10 294189 APN Ces5a 0.125 IGL02456 8 93528644 (GRCm38) C T splice site Het probably benign phenotype 2015-04-16
11 294176 APN Cfhr1 0.072 IGL02456 1 139556393 (GRCm38) N128K A C missense Het possibly damaging 0.877 phenotype 2015-04-16
12 294158 APN Clcn3 0.527 IGL02456 8 60941357 (GRCm38) D46G T C missense Het probably damaging 0.998 phenotype 2015-04-16
13 294174 APN Cntnap1 0.270 IGL02456 11 101178129 (GRCm38) I166S T G missense Het probably benign 0.305 phenotype 2015-04-16
14 294194 APN Cntnap3 0.055 IGL02456 13 64799058 (GRCm38) A T splice site Het probably benign phenotype 2015-04-16
15 294196 APN Cntnap5c 0.066 IGL02456 17 58407744 (GRCm38) T A splice site Het probably benign 2015-04-16
16 294159 APN Ddx23 1.000 IGL02456 15 98647549 (GRCm38) V626E A T missense Het probably damaging 0.999 phenotype 2015-04-16
17 294175 APN Gcm2 0.677 IGL02456 13 41103001 (GRCm38) Y424C T C missense Het probably benign 0.015 phenotype 2015-04-16
18 294183 APN Gm9964 0.180 IGL02456 11 79296370 (GRCm38) F84L A G missense Het probably damaging 0.985 2015-04-16
19 294172 APN Grn 0.494 IGL02456 11 102436104 (GRCm38) D509E T A missense Het probably benign 0.007 phenotype 2015-04-16
20 294162 APN Kdm5c IGL02456 X 152246318 (GRCm38) D343N G A missense Het probably damaging 1.000 phenotype 2015-04-16
21 294188 APN Ly75 0.000 IGL02456 2 60293781 (GRCm38) M1717I C T missense Het probably benign 0.090 phenotype 2015-04-16
22 294163 APN Map1a 0.311 IGL02456 2 121298653 (GRCm38) P133T C A missense Het probably damaging 1.000 phenotype 2015-04-16
23 294157 APN Mpp2 0.000 IGL02456 11 102059373 (GRCm38) A552S C A missense Het possibly damaging 0.716 phenotype 2015-04-16
24 294178 APN Mtr 1.000 IGL02456 13 12199094 (GRCm38) I897M T C missense Het probably damaging 0.981 phenotype 2015-04-16
25 294173 APN Npas3 0.920 IGL02456 12 54048767 (GRCm38) I337F A T missense Het probably damaging 0.993 phenotype 2015-04-16
26 294191 APN Nup85 1.000 IGL02456 11 115581865 (GRCm38) T C unclassified Het probably benign phenotype 2015-04-16
27 294151 APN Olfr118 0.057 IGL02456 17 37672449 (GRCm38) M142K T A missense Het possibly damaging 0.903 phenotype 2015-04-16
28 294153 APN Olfr325 0.059 IGL02456 11 58581198 (GRCm38) L118H T A missense Het possibly damaging 0.482 phenotype 2015-04-16
29 294160 APN Olfr517 0.115 IGL02456 7 108869050 (GRCm38) Y35H A G missense Het probably benign 0.190 phenotype 2015-04-16
30 294171 APN Olfr630 0.088 IGL02456 7 103755493 (GRCm38) I31F T A missense Het possibly damaging 0.938 phenotype 2015-04-16
31 294154 APN Olfr683 0.083 IGL02456 7 105143759 (GRCm38) N178S T C missense Het probably damaging 0.989 phenotype 2015-04-16
32 294169 APN Pdia4 0.000 IGL02456 6 47803495 (GRCm38) D301E A T missense Het probably benign 0.190 phenotype 2015-04-16
33 294180 APN Phf2 0.334 IGL02456 13 48828846 (GRCm38) G134C C A missense Het unknown phenotype 2015-04-16
34 294168 APN Polr2h 1.000 IGL02456 16 20720602 (GRCm38) L76H T A missense Het probably damaging 1.000 phenotype 2015-04-16
35 294185 APN Rbm47 0.229 IGL02456 5 66027021 (GRCm38) R80C G A missense Het probably damaging 1.000 phenotype 2015-04-16
36 294155 APN Sfmbt1 0.748 IGL02456 14 30785880 (GRCm38) S286P T C missense Het probably damaging 0.994 phenotype 2015-04-16
37 294197 APN Slc5a12 0.135 IGL02456 2 110616834 (GRCm38) T C splice site Het probably benign phenotype 2015-04-16
38 294167 APN Tacc2 0.000 IGL02456 7 130626261 (GRCm38) S1559P T C missense Het probably benign 0.350 phenotype 2015-04-16
39 294181 APN Tbc1d16 0.000 IGL02456 11 119210546 (GRCm38) H46P T G missense Het probably damaging 1.000 2015-04-16
40 294193 APN Tbck 0.324 IGL02456 3 132734714 (GRCm38) A G splice site Het probably benign phenotype 2015-04-16
41 294192 APN Tmtc4 0.000 IGL02456 14 122925962 (GRCm38) A T critical splice donor site 2 bp Het probably null 2015-04-16
42 294190 APN Ttc13 0.000 IGL02456 8 124690361 (GRCm38) T C critical splice acceptor site Het probably null 2015-04-16
43 294195 APN Ttc17 0.528 IGL02456 2 94362785 (GRCm38) T C splice site Het probably benign 2015-04-16
44 294150 APN Vmn1r121 0.070 IGL02456 7 21098513 (GRCm38) M1L T A start codon destroyed Het possibly damaging 0.924 2015-04-16
45 294182 APN Vps13c 0.000 IGL02456 9 67952976 (GRCm38) S2825P T C missense Het probably damaging 1.000 phenotype 2015-04-16
46 294177 APN Zan 0.078 IGL02456 5 137446844 (GRCm38) S1718A A C missense Het unknown phenotype 2015-04-16
47 294165 APN Zfp39 0.211 IGL02456 11 58902800 (GRCm38) Y37* G T nonsense Het probably null phenotype 2015-04-16
48 294161 APN Zfp407 1.000 IGL02456 18 84558641 (GRCm38) N1449S T C missense Het probably damaging 0.996 phenotype 2015-04-16
49 294187 APN Zhx2 0.310 IGL02456 15 57823639 (GRCm38) D801E C A missense Het possibly damaging 0.720 phenotype 2015-04-16
[records 1 to 49 of 49]