Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
5 are Possibly Damaging.
9 are Probably Damaging.
8 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 299127 APN Arhgef12 0.935 IGL02574 9 43005623 D409G T C missense Het probably damaging 0.989 phenotype 04/16/2015
2 299139 APN AW551984 0.073 IGL02574 9 39589086 L792R A C missense Het possibly damaging 0.906 04/16/2015
3 299143 APN Cep192 0.000 IGL02574 18 67841279 E1151G A G missense Het probably damaging 0.986 04/16/2015
4 299123 APN Cfap44 0.000 IGL02574 16 44481383 P1828Q C A missense Het probably damaging 0.999 phenotype 04/16/2015
5 299147 APN Chid1 0.078 IGL02574 7 141496690 A T splice site Het probably benign 04/16/2015
6 299128 APN Col6a6 0.106 IGL02574 9 105782191 L518F C A missense Het probably damaging 1.000 04/16/2015
7 299125 APN Ctsz 0.167 IGL02574 2 174429098 R201K C T missense Het probably benign 0.156 phenotype 04/16/2015
8 299131 APN D430042O09Rik 0.000 IGL02574 7 125829753 T516A A G missense Het possibly damaging 0.482 phenotype 04/16/2015
9 299134 APN Diras1 0.250 IGL02574 10 81022285 Y44C T C missense Het probably damaging 1.000 phenotype 04/16/2015
10 299140 APN Grip1 1.000 IGL02574 10 119942913 V159A T C missense Het probably damaging 0.997 phenotype 04/16/2015
11 299146 APN Hpd 0.156 IGL02574 5 123179357 T C splice site Het probably benign phenotype 04/16/2015
12 299124 APN Jag2 1.000 IGL02574 12 112915511 N463S T C missense Het probably benign 0.321 phenotype 04/16/2015
13 299148 APN Kmt2a 1.000 IGL02574 9 44830513 C A splice site Het probably benign phenotype 04/16/2015
14 299136 APN Myo5a 0.947 IGL02574 9 75211147 N1619D A G missense Het probably benign 0.001 phenotype 04/16/2015
15 299145 APN Ncbp1 1.000 IGL02574 4 46168449 A G critical splice acceptor site Het probably null phenotype 04/16/2015
16 299132 APN Olfr103 0.066 IGL02574 17 37336524 A236E G T missense Het probably damaging 0.999 phenotype 04/16/2015
17 299126 APN Olfr133 0.137 IGL02574 17 38149389 T267I C T missense Het possibly damaging 0.558 phenotype 04/16/2015
18 299142 APN Pacsin2 0.000 IGL02574 15 83388663 A154E G T missense Het possibly damaging 0.814 phenotype 04/16/2015
19 299144 APN Plcd4 0.000 IGL02574 1 74564380 I647F A T missense Het probably damaging 1.000 phenotype 04/16/2015
20 299137 APN Prdm10 1.000 IGL02574 9 31357293 A846V C T missense Het probably damaging 0.999 phenotype 04/16/2015
21 299135 APN Ptgs2 0.701 IGL02574 1 150102775 G213* G T nonsense Het probably null phenotype 04/16/2015
22 299129 APN Rcan3 0.113 IGL02574 4 135425395 S5N C T missense Het probably benign 0.053 04/16/2015
23 299130 APN Rnf123 0.223 IGL02574 9 108068302 R390* G A nonsense Het probably null phenotype 04/16/2015
24 299138 APN Serpinc1 1.000 IGL02574 1 161002459 N465S A G missense Het probably benign 0.002 phenotype 04/16/2015
25 299133 APN Slc40a1 1.000 IGL02574 1 45912374 I208V T C missense Het possibly damaging 0.771 phenotype 04/16/2015
26 299141 APN Vcl 1.000 IGL02574 14 20929575 Q19* C T nonsense Het probably null phenotype 04/16/2015
[records 1 to 26 of 26]